Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23129 |
|---|---|
| ensemblid | ENSG00000004399.13 |
| hgncid | 9107 |
| symbol | PLXND1 |
| name | plexin D1 |
| refseq_nuc | NM_015103.3 |
| refseq_prot | NP_055918.3 |
| ensembl_nuc | ENST00000324093.9 |
| ensembl_prot | ENSP00000317128.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129555214 |
| end | 129606676 |
| strand | - |
| ver | v1.2 |
| region | chr3:129555214-129606676 |
| region5000 | chr3:129550214-129611676 |
| regionname0 | PLXND1_chr3_129555214_129606676 |
| regionname5000 | PLXND1_chr3_129550214_129611676 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1925 | 187 | 18 | 32 | 106 | 6 | 25 | 86 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002 | 0/0 | 1925 | 112 | 34 | 17 | 51 | 2 | 8 | 35 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003 | 0/1 | 1925 | 42 | 13 | 16 | 0 | 6 | 6 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004 | 0/0 | 1925 | 29 | 6 | 3 | 15 | 1 | 4 | 13 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0005 | 0/0 | 1925 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006 | 0/0 | 1925 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0007 | 0/0 | 1925 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0008 | 0/0 | 1925 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0009 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0010 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0011 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0012 | 0/0 | 1925 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0013 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0014 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0015 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0016 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0017 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0018 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0019 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0020 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0021 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0022 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0023 | 1/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0024 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0025 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0026 | 0/0 | 1925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0027 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0028 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0029 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0030 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0031 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0032 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0033 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 5778 | 110 | 8 | 27 | 54 | 6 | 15 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0002 | 0/0 | 5778 | 53 | 2 | 5 | 39 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0003 | 0/0 | 5778 | 44 | 0 | 0 | 40 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0004 | 0/0 | 5778 | 24 | 3 | 1 | 15 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0005 | 0/0 | 5778 | 23 | 9 | 8 | 1 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0006 | 0/0 | 5778 | 13 | 11 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0007 | 0/0 | 5778 | 13 | 2 | 5 | 0 | 5 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0008 | 0/1 | 5778 | 12 | 1 | 8 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0009 | 0/0 | 5778 | 10 | 0 | 4 | 6 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0010 | 0/0 | 5778 | 7 | 0 | 3 | 0 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0011 | 0/0 | 5778 | 6 | 4 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0012 | 0/0 | 5778 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0013 | 0/0 | 5778 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0014 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0015 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0016 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0017 | 0/0 | 5778 | 4 | 2 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0018 | 0/0 | 5778 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0019 | 0/0 | 5778 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0020 | 0/0 | 5778 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0021 | 0/0 | 5778 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0022 | 0/0 | 5778 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0023 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0024 | 0/0 | 5778 | 2 | 0 | 0 | 0 | 2 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0025 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0026 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0027 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0028 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0029 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0030 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0031 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0032 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0033 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0034 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0035 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0036 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0037 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0038 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0039 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0040 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0041 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0042 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0043 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0044 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0045 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0046 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0047 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0048 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0049 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0050 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0051 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0052 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0053 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0054 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0055 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0056 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0057 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0058 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0059 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0060 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0061 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0062 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0063 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0064 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0065 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0066 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0067 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0068 | 1/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0069 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0070 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| c0071 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1136 | 234 | 53 | 46 | 85 | 14 | 35 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0002 | 0/0 | 1136 | 64 | 5 | 7 | 45 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0003 | 0/0 | 1136 | 62 | 0 | 3 | 55 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0004 | 0/1 | 1136 | 30 | 15 | 10 | 0 | 3 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0005 | 0/0 | 1136 | 6 | 6 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0006 | 0/0 | 1136 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0007 | 0/0 | 1136 | 3 | 1 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0008 | 0/0 | 1136 | 3 | 1 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0009 | 0/0 | 1136 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0010 | 0/0 | 1136 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0011 | 0/0 | 1136 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0012 | 0/0 | 1136 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0013 | 0/0 | 1136 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| t0014 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0002 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0011 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0021 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5778 | 110 | 8 | 27 | 54 | 6 | 15 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0002 | 0/0 | 5778 | 53 | 2 | 5 | 39 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0011 | 0/0 | 5778 | 6 | 4 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0013 | 0/0 | 5778 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0020 | 0/0 | 5778 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0028 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0039 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0045 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0047 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0048 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0056 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0061 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0064 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0069 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0003 | 0/0 | 5778 | 44 | 0 | 0 | 40 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0005 | 0/0 | 5778 | 23 | 9 | 8 | 1 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0006 | 0/0 | 5778 | 13 | 11 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0009 | 0/0 | 5778 | 10 | 0 | 4 | 6 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0012 | 0/0 | 5778 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0015 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0017 | 0/0 | 5778 | 4 | 2 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0042 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0043 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0049 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0050 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0052 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0066 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0070 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0007 | 0/0 | 5778 | 13 | 2 | 5 | 0 | 5 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0008 | 0/1 | 5778 | 12 | 1 | 8 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0010 | 0/0 | 5778 | 7 | 0 | 3 | 0 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0014 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0018 | 0/0 | 5778 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0051 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0004 | 0/0 | 5778 | 24 | 3 | 1 | 15 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0019 | 0/0 | 5778 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0035 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0067 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0005c0016 | 0/0 | 5778 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0023 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0040 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0041 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0007c0021 | 0/0 | 5778 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0008c0022 | 0/0 | 5778 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0009c0032 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0009c0033 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0010c0026 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0011c0029 | 0/0 | 5778 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0012c0024 | 0/0 | 5778 | 2 | 0 | 0 | 0 | 2 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0013c0053 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0013c0054 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0014c0025 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0015c0027 | 0/0 | 5778 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0016c0030 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0017c0058 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0018c0057 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0019c0055 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0020c0037 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0021c0038 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0022c0059 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0023c0068 | 1/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0024c0044 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0025c0065 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0026c0062 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0027c0063 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0028c0031 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0029c0046 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0030c0060 | 0/0 | 5778 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0031c0036 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0032c0034 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0033c0071 | 0/0 | 5778 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6913 | 106 | 7 | 25 | 54 | 6 | 14 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0001t0008 | 0/0 | 6913 | 3 | 1 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0001t0013 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0002t0002 | 0/0 | 6913 | 52 | 2 | 5 | 38 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0002t0012 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0011t0001 | 0/0 | 6913 | 6 | 4 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0013t0003 | 0/0 | 6913 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0020t0001 | 0/0 | 6913 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0028t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0039t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0045t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0047t0002 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0048t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0056t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0061t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0064t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0001c0069t0011 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0003t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0003t0003 | 0/0 | 6913 | 43 | 0 | 0 | 39 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0005t0001 | 0/0 | 6913 | 23 | 9 | 8 | 1 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0006t0001 | 0/0 | 6913 | 13 | 11 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0009t0001 | 0/0 | 6913 | 3 | 0 | 1 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0009t0003 | 0/0 | 6913 | 7 | 0 | 3 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0012t0001 | 0/0 | 6913 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0015t0006 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0017t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0017t0007 | 0/0 | 6913 | 3 | 1 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0042t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0043t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0049t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0050t0009 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0052t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0066t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0002c0070t0011 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0007t0001 | 0/0 | 6913 | 13 | 2 | 5 | 0 | 5 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0008t0004 | 0/1 | 6913 | 12 | 1 | 8 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0010t0001 | 0/0 | 6913 | 7 | 0 | 3 | 0 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0014t0004 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0018t0005 | 0/0 | 6913 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0003c0051t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0004t0001 | 0/0 | 6913 | 24 | 3 | 1 | 15 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0019t0004 | 0/0 | 6913 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0035t0004 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0004c0067t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0005c0016t0001 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0023t0001 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0040t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0006c0041t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0007c0021t0002 | 0/0 | 6913 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0007c0021t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0008c0022t0001 | 0/0 | 6913 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0009c0032t0005 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0009c0033t0005 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0010c0026t0004 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0011c0029t0010 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0012c0024t0004 | 0/0 | 6913 | 2 | 0 | 0 | 0 | 2 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0013c0053t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0013c0054t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0014c0025t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0015c0027t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0016c0030t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0017c0058t0014 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0018c0057t0009 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0019c0055t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0020c0037t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0021c0038t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0022c0059t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0023c0068t0001 | 1/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0024c0044t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0025c0065t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0026c0062t0002 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0027c0063t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0028c0031t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0029c0046t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0030c0060t0002 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0031c0036t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0032c0034t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| a0033c0071t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | copy fasta | chr3 | 129550214 | 129611676 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0008g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0001t0013g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0002t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0011t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0011t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0011t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0013t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0013t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0020t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0020t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0020t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0028t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0039t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0045t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0047t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0048t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0056t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0061t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0064t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0001c0069t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0005t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0006t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0003g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0009t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0012t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0012t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0012t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0012t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0012t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0015t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0015t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0015t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0015t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0015t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0017t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0017t0007g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0017t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0042t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0043t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0049t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0050t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0052t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0066t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0002c0070t0011g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0007t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0008t0004g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0010t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0010t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0010t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0010t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0014t0004g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0014t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0014t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0014t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0018t0005g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0018t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0018t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0003c0051t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0019t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0019t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0019t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0035t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0004c0067t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0005c0016t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0005c0016t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0005c0016t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0006c0023t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0006c0023t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0006c0040t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0006c0041t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0007c0021t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0007c0021t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0008c0022t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0008c0022t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0009c0032t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0009c0033t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0010c0026t0004g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0011c0029t0010g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0012c0024t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0012c0024t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0013c0053t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0013c0054t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0014c0025t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0014c0025t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0015c0027t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0015c0027t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0016c0030t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0017c0058t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0018c0057t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0019c0055t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0020c0037t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0021c0038t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0022c0059t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0023c0068t0001g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0024c0044t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0025c0065t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0026c0062t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0027c0063t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0028c0031t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0029c0046t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0030c0060t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0031c0036t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0032c0034t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| a0033c0071t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00140 | hp1 | a0002 | c0017 | t0007 | g0143 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00140 | hp2 | a0003 | c0007 | t0001 | g0103 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00280 | hp1 | a0003 | c0007 | t0001 | g0026 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00323 | hp1 | a0003 | c0008 | t0004 | g0177 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00408 | hp2 | a0004 | c0004 | t0001 | g0252 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00438 | hp1 | a0001 | c0061 | t0001 | g0077 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00438 | hp2 | a0001 | c0011 | t0001 | g0212 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00597 | hp2 | a0002 | c0066 | t0002 | g0092 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00609 | hp1 | a0001 | c0028 | t0001 | g0025 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00621 | hp1 | a0002 | c0003 | t0003 | g0046 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0173 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00639 | hp2 | a0004 | c0019 | t0004 | g0249 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00642 | hp1 | a0003 | c0007 | t0001 | g0080 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00642 | hp2 | a0003 | c0008 | t0004 | g0039 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0045 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00733 | hp1 | a0001 | c0001 | t0013 | g0147 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00733 | hp2 | a0003 | c0007 | t0001 | g0009 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00735 | hp1 | a0002 | c0050 | t0009 | g0120 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00735 | hp2 | a0003 | c0007 | t0001 | g0099 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00738 | hp1 | a0002 | c0017 | t0007 | g0033 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG00738 | hp2 | a0002 | c0005 | t0001 | g0055 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01069 | hp1 | a0002 | c0005 | t0001 | g0028 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01069 | hp2 | a0003 | c0007 | t0001 | g0027 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01070 | hp2 | a0003 | c0008 | t0004 | g0038 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01071 | hp1 | a0003 | c0008 | t0004 | g0038 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01071 | hp2 | a0002 | c0005 | t0001 | g0028 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01099 | hp1 | a0003 | c0010 | t0001 | g0263 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01099 | hp2 | a0002 | c0005 | t0001 | g0150 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01109 | hp1 | a0003 | c0007 | t0001 | g0009 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01109 | hp2 | a0002 | c0006 | t0001 | g0010 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01167 | hp1 | a0002 | c0005 | t0001 | g0291 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01168 | hp1 | a0003 | c0008 | t0004 | g0294 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01169 | hp1 | a0002 | c0005 | t0001 | g0055 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01175 | hp2 | a0003 | c0008 | t0004 | g0017 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01192 | hp1 | a0003 | c0008 | t0004 | g0179 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01243 | hp1 | a0007 | c0021 | t0002 | g0023 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01255 | hp1 | a0002 | c0006 | t0001 | g0007 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01255 | hp2 | a0002 | c0009 | t0003 | g0232 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01257 | hp1 | a0003 | c0010 | t0001 | g0050 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01258 | hp2 | a0003 | c0010 | t0001 | g0050 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01346 | hp1 | a0002 | c0005 | t0001 | g0004 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01346 | hp2 | a0026 | c0062 | t0002 | g0096 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01433 | hp2 | a0003 | c0008 | t0004 | g0293 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01496 | hp1 | a0002 | c0012 | t0001 | g0281 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01515 | hp1 | a0002 | c0005 | t0001 | g0135 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01515 | hp2 | a0003 | c0007 | t0001 | g0009 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01516 | hp1 | a0012 | c0024 | t0004 | g0140 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01516 | hp2 | a0008 | c0022 | t0001 | g0061 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01517 | hp1 | a0012 | c0024 | t0004 | g0178 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01517 | hp2 | a0003 | c0007 | t0001 | g0027 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01884 | hp1 | a0002 | c0005 | t0001 | g0287 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01891 | hp1 | a0005 | c0016 | t0001 | g0307 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01891 | hp2 | a0002 | c0012 | t0001 | g0278 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01975 | hp2 | a0002 | c0009 | t0003 | g0018 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01978 | hp1 | a0002 | c0009 | t0003 | g0018 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01978 | hp2 | a0002 | c0005 | t0001 | g0148 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01981 | hp2 | a0004 | c0035 | t0004 | g0250 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02015 | hp1 | a0004 | c0004 | t0001 | g0019 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02055 | hp1 | a0002 | c0015 | t0006 | g0121 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02055 | hp2 | a0002 | c0006 | t0001 | g0289 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0233 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02074 | hp2 | a0002 | c0003 | t0003 | g0218 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0210 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0046 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0225 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02145 | hp1 | a0002 | c0017 | t0007 | g0033 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02145 | hp2 | a0002 | c0015 | t0006 | g0146 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02148 | hp2 | a0004 | c0004 | t0001 | g0245 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02155 | hp2 | a0002 | c0003 | t0003 | g0234 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02165 | hp1 | a0022 | c0059 | t0002 | g0086 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02257 | hp1 | a0017 | c0058 | t0014 | g0270 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02257 | hp2 | a0006 | c0023 | t0001 | g0144 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02258 | hp1 | a0003 | c0018 | t0005 | g0051 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02258 | hp2 | a0003 | c0008 | t0004 | g0017 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02280 | hp2 | a0005 | c0016 | t0001 | g0022 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02293 | hp2 | a0002 | c0009 | t0001 | g0229 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02451 | hp1 | a0002 | c0012 | t0001 | g0052 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0224 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02523 | hp2 | a0027 | c0063 | t0002 | g0074 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02602 | hp2 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02615 | hp1 | a0002 | c0017 | t0004 | g0275 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02622 | hp1 | a0003 | c0007 | t0001 | g0009 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02622 | hp2 | a0020 | c0037 | t0001 | g0257 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02630 | hp1 | a0004 | c0067 | t0004 | g0303 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0272 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02647 | hp2 | a0003 | c0014 | t0004 | g0053 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02698 | hp1 | a0006 | c0041 | t0001 | g0261 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02698 | hp2 | a0003 | c0007 | t0001 | g0026 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02717 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02717 | hp2 | a0010 | c0026 | t0004 | g0054 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02723 | hp1 | a0009 | c0033 | t0005 | g0267 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02723 | hp2 | a0003 | c0014 | t0004 | g0292 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0036 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02735 | hp2 | a0002 | c0005 | t0001 | g0127 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02809 | hp1 | a0002 | c0012 | t0001 | g0282 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02809 | hp2 | a0001 | c0047 | t0002 | g0283 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02818 | hp1 | a0002 | c0015 | t0006 | g0118 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02818 | hp2 | a0002 | c0049 | t0001 | g0280 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02886 | hp1 | a0002 | c0070 | t0011 | g0305 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0246 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02896 | hp1 | a0001 | c0011 | t0001 | g0015 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02896 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02897 | hp1 | a0002 | c0005 | t0001 | g0276 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02897 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02922 | hp1 | a0006 | c0023 | t0001 | g0138 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02922 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02965 | hp1 | a0002 | c0015 | t0006 | g0119 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02965 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02970 | hp1 | a0003 | c0014 | t0004 | g0284 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0244 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02976 | hp1 | a0003 | c0014 | t0004 | g0288 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02976 | hp2 | a0003 | c0014 | t0004 | g0053 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03017 | hp2 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03041 | hp1 | a0006 | c0040 | t0004 | g0262 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03041 | hp2 | a0002 | c0012 | t0001 | g0052 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03139 | hp1 | a0004 | c0019 | t0004 | g0247 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03139 | hp2 | a0003 | c0018 | t0005 | g0051 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03195 | hp1 | a0002 | c0015 | t0006 | g0117 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0004 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03209 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03209 | hp2 | a0005 | c0016 | t0001 | g0308 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03225 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0299 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03239 | hp1 | a0003 | c0008 | t0004 | g0039 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03239 | hp2 | a0008 | c0022 | t0001 | g0060 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03453 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03453 | hp2 | a0011 | c0029 | t0010 | g0057 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03486 | hp1 | a0001 | c0011 | t0001 | g0015 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03486 | hp2 | a0003 | c0051 | t0004 | g0279 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0013 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0108 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03492 | hp1 | a0002 | c0003 | t0003 | g0013 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03516 | hp1 | a0004 | c0019 | t0004 | g0240 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0004 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03540 | hp1 | a0005 | c0016 | t0001 | g0022 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03540 | hp2 | a0001 | c0069 | t0011 | g0306 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03579 | hp1 | a0003 | c0018 | t0005 | g0260 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03579 | hp2 | a0007 | c0021 | t0004 | g0069 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03654 | hp1 | a0002 | c0003 | t0003 | g0208 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03654 | hp2 | a0024 | c0044 | t0001 | g0131 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03688 | hp1 | a0004 | c0004 | t0001 | g0239 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03704 | hp1 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0301 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03834 | hp2 | a0002 | c0005 | t0001 | g0155 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03927 | hp2 | a0004 | c0004 | t0001 | g0254 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03942 | hp1 | a0002 | c0005 | t0001 | g0126 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0109 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0089 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04115 | hp2 | a0032 | c0034 | t0001 | g0242 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04184 | hp1 | a0001 | c0020 | t0001 | g0166 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04184 | hp2 | a0029 | c0046 | t0001 | g0182 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04199 | hp1 | a0001 | c0020 | t0001 | g0132 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04199 | hp2 | a0003 | c0010 | t0001 | g0265 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04204 | hp2 | a0004 | c0004 | t0001 | g0241 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04228 | hp1 | a0002 | c0005 | t0001 | g0139 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG04228 | hp2 | a0004 | c0004 | t0001 | g0248 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18522 | hp1 | a0019 | c0055 | t0001 | g0122 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18522 | hp2 | a0002 | c0006 | t0001 | g0269 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0214 | EAS | CHB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18906 | hp1 | a0001 | c0045 | t0001 | g0149 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0226 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18940 | hp2 | a0001 | c0002 | t0012 | g0095 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0043 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18942 | hp2 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18943 | hp2 | a0004 | c0004 | t0001 | g0056 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18944 | hp1 | a0002 | c0003 | t0003 | g0236 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0056 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18947 | hp2 | a0002 | c0009 | t0003 | g0219 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18950 | hp1 | a0004 | c0004 | t0001 | g0019 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18951 | hp2 | a0014 | c0025 | t0001 | g0255 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0193 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18954 | hp2 | a0002 | c0003 | t0003 | g0237 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18959 | hp1 | a0021 | c0038 | t0003 | g0213 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18959 | hp2 | a0014 | c0025 | t0001 | g0154 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18960 | hp2 | a0002 | c0003 | t0003 | g0048 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18965 | hp1 | a0013 | c0053 | t0003 | g0221 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18965 | hp2 | a0013 | c0054 | t0003 | g0220 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18966 | hp2 | a0002 | c0052 | t0003 | g0168 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0045 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18969 | hp2 | a0002 | c0009 | t0001 | g0228 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18973 | hp1 | a0004 | c0004 | t0001 | g0194 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18973 | hp2 | a0002 | c0003 | t0003 | g0048 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18974 | hp1 | a0004 | c0004 | t0001 | g0253 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18974 | hp2 | a0015 | c0027 | t0001 | g0201 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18977 | hp1 | a0001 | c0011 | t0001 | g0215 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18977 | hp2 | a0004 | c0004 | t0001 | g0049 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18979 | hp1 | a0001 | c0028 | t0001 | g0025 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18980 | hp1 | a0002 | c0005 | t0001 | g0188 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18980 | hp2 | a0002 | c0009 | t0001 | g0217 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18981 | hp2 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18984 | hp2 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18988 | hp2 | a0031 | c0036 | t0001 | g0238 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18992 | hp2 | a0015 | c0027 | t0001 | g0195 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18993 | hp1 | a0016 | c0030 | t0001 | g0058 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18993 | hp2 | a0002 | c0003 | t0003 | g0044 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18994 | hp1 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18995 | hp1 | a0002 | c0003 | t0003 | g0302 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18999 | hp1 | a0004 | c0004 | t0001 | g0251 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18999 | hp2 | a0002 | c0003 | t0003 | g0222 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19000 | hp1 | a0002 | c0003 | t0003 | g0206 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19003 | hp2 | a0002 | c0009 | t0003 | g0047 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0216 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19005 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19007 | hp1 | a0004 | c0004 | t0001 | g0049 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0235 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19011 | hp2 | a0002 | c0003 | t0003 | g0044 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19012 | hp1 | a0004 | c0004 | t0001 | g0298 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19030 | hp1 | a0002 | c0006 | t0001 | g0123 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19043 | hp1 | a0030 | c0060 | t0002 | g0070 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19043 | hp2 | a0001 | c0056 | t0001 | g0259 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0211 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19057 | hp2 | a0002 | c0003 | t0003 | g0300 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19058 | hp1 | a0033 | c0071 | t0003 | g0309 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19060 | hp1 | a0001 | c0064 | t0001 | g0093 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19060 | hp2 | a0002 | c0003 | t0003 | g0207 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19062 | hp1 | a0001 | c0048 | t0002 | g0134 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19062 | hp2 | a0001 | c0013 | t0003 | g0125 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19063 | hp2 | a0002 | c0043 | t0003 | g0223 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19065 | hp2 | a0025 | c0065 | t0002 | g0090 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19066 | hp2 | a0004 | c0004 | t0001 | g0019 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19068 | hp1 | a0002 | c0042 | t0003 | g0209 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19074 | hp1 | a0001 | c0039 | t0002 | g0231 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19077 | hp1 | a0002 | c0009 | t0003 | g0018 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19084 | hp2 | a0002 | c0009 | t0003 | g0047 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0043 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19087 | hp1 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19087 | hp2 | a0028 | c0031 | t0002 | g0059 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19090 | hp1 | a0004 | c0004 | t0001 | g0243 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19090 | hp2 | a0004 | c0004 | t0001 | g0297 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19240 | hp1 | a0002 | c0012 | t0001 | g0290 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA19240 | hp2 | a0007 | c0021 | t0002 | g0023 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20129 | hp1 | a0003 | c0018 | t0005 | g0258 | AFR | ASW | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ASW | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20805 | hp1 | a0003 | c0007 | t0001 | g0102 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20805 | hp2 | a0004 | c0004 | t0001 | g0197 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20905 | hp1 | a0001 | c0020 | t0001 | g0167 | SAS | GIH | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0104 | SAS | GIH | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG01123 | hp2 | a0003 | c0008 | t0004 | g0017 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02109 | hp1 | a0005 | c0016 | t0001 | g0022 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02109 | hp2 | a0002 | c0005 | t0001 | g0277 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02486 | hp2 | a0009 | c0032 | t0005 | g0268 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02559 | hp1 | a0010 | c0026 | t0004 | g0054 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG02559 | hp2 | a0011 | c0029 | t0010 | g0057 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03471 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG03471 | hp2 | a0018 | c0057 | t0009 | g0286 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG06807 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| HG06807 | hp2 | a0002 | c0006 | t0001 | g0285 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA20300 | hp2 | a0003 | c0007 | t0001 | g0266 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0008 | t0004 | g0296 | REF | REF | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| homoSapiens_grch38 | hp1 | a0023 | c0068 | t0001 | g0304 | REF | REF | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129556419
|
C | T | 1 | a0027 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.5671G>A | p.Ala1891Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 5708/6913 | 5671/5778 | 1891/1925 | chr3 | 129556419 | ||
| chr3:129557159
|
C | T | 1 | a0026 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.5510G>A | p.Arg1837His | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/36 | 5547/6913 | 5510/5778 | 1837/1925 | chr3 | 129557159 | ||
| chr3:129563137
|
C | T | 32 | a0001a0002a0003others(29): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
missense_variant | MODERATE | c.4625G>A | p.Ser1542Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/36 | 4662/6913 | 4625/5778 | 1542/1925 | chr3 | 129563137 | ||
| chr3:129565975
|
A | C | 7 | a0003a0006a0007others(4): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
missense_variant | MODERATE | c.4234T>G | p.Leu1412Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/36 | 4271/6913 | 4234/5778 | 1412/1925 | chr3 | 129565975 | ||
| chr3:129565993
|
T | G | 1 | a0031 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.4216A>C | p.Met1406Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/36 | 4253/6913 | 4216/5778 | 1406/1925 | chr3 | 129565993 | ||
| chr3:129567745
|
A | C | 1 | a0028 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.3926T>G | p.Leu1309Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/36 | 3963/6913 | 3926/5778 | 1309/1925 | chr3 | 129567745 | ||
| chr3:129569927
|
C | T | 1 | a0029 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.3781G>A | p.Ala1261Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/36 | 3818/6913 | 3781/5778 | 1261/1925 | chr3 | 129569927 | ||
| chr3:129571135
|
G | A | 1 | a0012 | 2 | HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.3505C>T | p.Arg1169Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3542/6913 | 3505/5778 | 1169/1925 | chr3 | 129571135 | ||
| chr3:129571725
|
A | G | 1 | a0030 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3197T>C | p.Met1066Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3234/6913 | 3197/5778 | 1066/1925 | chr3 | 129571725 | ||
| chr3:129571843
|
G | A | 1 | a0025 | 1 | NA19065.hp2 | missense_variant&splice_region_variant | MODERATE | c.3079C>T | p.Arg1027Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3116/6913 | 3079/5778 | 1027/1925 | chr3 | 129571843 | ||
| chr3:129572861
|
C | T | 1 | a0024 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2918G>A | p.Arg973Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/36 | 2955/6913 | 2918/5778 | 973/1925 | chr3 | 129572861 | ||
| chr3:129574340
|
T | C | 31 | a0001a0002a0003others(28): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
missense_variant | MODERATE | c.2681A>G | p.His894Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2718/6913 | 2681/5778 | 894/1925 | chr3 | 129574340 | ||
| chr3:129574369
|
C | T | 1 | a0022 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2652G>A | p.Met884Ile | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2689/6913 | 2652/5778 | 884/1925 | chr3 | 129574369 | ||
| chr3:129574413
|
T | C | 17 | a0002a0003a0004others(14): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
missense_variant | MODERATE | c.2608A>G | p.Met870Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2645/6913 | 2608/5778 | 870/1925 | chr3 | 129574413 | ||
| chr3:129575498
|
C | T | 1 | a0021 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.2501G>A | p.Arg834Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/36 | 2538/6913 | 2501/5778 | 834/1925 | chr3 | 129575498 | ||
| chr3:129575549
|
C | T | 1 | a0020 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2450G>A | p.Arg817Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/36 | 2487/6913 | 2450/5778 | 817/1925 | chr3 | 129575549 | ||
| chr3:129584393
|
G | C | 1 | a0013 | 2 | NA18965.hp1 NA18965.hp2 |
missense_variant | MODERATE | c.2021C>G | p.Pro674Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 2058/6913 | 2021/5778 | 674/1925 | chr3 | 129584393 | ||
| chr3:129584543
|
G | A | 1 | a0019 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1871C>T | p.Ser624Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 1908/6913 | 1871/5778 | 624/1925 | chr3 | 129584543 | ||
| chr3:129585954
|
G | A | 5 | a0004a0015a0016others(2): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
missense_variant&splice_region_variant | MODERATE | c.1849C>T | p.Pro617Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/36 | 1886/6913 | 1849/5778 | 617/1925 | chr3 | 129585954 | ||
| chr3:129586616
|
C | A | 1 | a0014 | 2 | NA18951.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.1592G>T | p.Gly531Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1629/6913 | 1592/5778 | 531/1925 | chr3 | 129586616 | ||
| chr3:129586617
|
C | T | 6 | a0004a0005a0015others(3): Show | 39 | HG00408.hp2 HG00639.hp2 HG01891.hp1 others(36): Show |
missense_variant | MODERATE | c.1591G>A | p.Gly531Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1628/6913 | 1591/5778 | 531/1925 | chr3 | 129586617 | ||
| chr3:129586664
|
T | C | 2 | a0010a0018 | 3 | HG02559.hp1 HG02717.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1544A>G | p.Tyr515Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1581/6913 | 1544/5778 | 515/1925 | chr3 | 129586664 | ||
| chr3:129586695
|
C | G | 2 | a0009a0017 | 3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.1513G>C | p.Val505Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1550/6913 | 1513/5778 | 505/1925 | chr3 | 129586695 | ||
| chr3:129586697
|
T | C | 1 | a0015 | 2 | NA18974.hp2 NA18992.hp2 |
missense_variant | MODERATE | c.1511A>G | p.Gln504Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1548/6913 | 1511/5778 | 504/1925 | chr3 | 129586697 | ||
| chr3:129586707
|
C | T | 1 | a0007 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1501G>A | p.Glu501Lys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1538/6913 | 1501/5778 | 501/1925 | chr3 | 129586707 | ||
| chr3:129605765
|
C | G | 1 | a0008 | 2 | HG01516.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.875G>C | p.Gly292Ala | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 912/6913 | 875/5778 | 292/1925 | chr3 | 129605765 | ||
| chr3:129605787
|
G | A | 1 | a0033 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.853C>T | p.His285Tyr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 890/6913 | 853/5778 | 285/1925 | chr3 | 129605787 | ||
| chr3:129606477
|
A | G | 1 | a0016 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.163T>C | p.Ser55Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 200/6913 | 163/5778 | 55/1925 | chr3 | 129606477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129556363
|
C | T | 25 | a0001c0002a0001c0039a0001c0047others(22): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
synonymous_variant | LOW | c.5727G>A | p.Gln1909Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 5764/6913 | 5727/5778 | 1909/1925 | chr3 | 129556363 | ||
| chr3:129556632
|
C | T | 1 | a0003c0051 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.5646G>A | p.Lys1882Lys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/36 | 5683/6913 | 5646/5778 | 1882/1925 | chr3 | 129556632 | ||
| chr3:129559661
|
T | G | 1 | a0002c0042 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.5256A>C | p.Gly1752Gly | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/36 | 5293/6913 | 5256/5778 | 1752/1925 | chr3 | 129559661 | ||
| chr3:129562875
|
C | T | 12 | a0001c0002a0001c0039a0001c0047others(9): Show | 64 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(61): Show |
synonymous_variant | LOW | c.4737G>A | p.Thr1579Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/36 | 4774/6913 | 4737/5778 | 1579/1925 | chr3 | 129562875 | ||
| chr3:129567516
|
G | A | 1 | a0002c0043 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.4062C>T | p.Phe1354Phe | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/36 | 4099/6913 | 4062/5778 | 1354/1925 | chr3 | 129567516 | ||
| chr3:129567570
|
G | C | 50 | a0001c0002a0001c0013a0001c0028others(47): Show | 252 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
synonymous_variant | LOW | c.4008C>G | p.Leu1336Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/36 | 4045/6913 | 4008/5778 | 1336/1925 | chr3 | 129567570 | ||
| chr3:129567792
|
G | A | 24 | a0001c0013a0001c0069a0002c0003others(21): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
synonymous_variant | LOW | c.3879C>T | p.Phe1293Phe | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/36 | 3916/6913 | 3879/5778 | 1293/1925 | chr3 | 129567792 | ||
| chr3:129570909
|
C | T | 12 | a0002c0006a0002c0012a0002c0015others(9): Show | 63 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(60): Show |
synonymous_variant | LOW | c.3627G>A | p.Gln1209Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/36 | 3664/6913 | 3627/5778 | 1209/1925 | chr3 | 129570909 | ||
| chr3:129571244
|
G | A | 12 | a0001c0002a0001c0028a0001c0039others(9): Show | 65 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
synonymous_variant | LOW | c.3396C>T | p.Asn1132Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3433/6913 | 3396/5778 | 1132/1925 | chr3 | 129571244 | ||
| chr3:129571259
|
G | A | 1 | a0009c0033 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3381C>T | p.Pro1127Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3418/6913 | 3381/5778 | 1127/1925 | chr3 | 129571259 | ||
| chr3:129571706
|
C | T | 1 | a0001c0045 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3216G>A | p.Thr1072Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3253/6913 | 3216/5778 | 1072/1925 | chr3 | 129571706 | ||
| chr3:129572656
|
G | A | 12 | a0001c0069a0002c0006a0002c0012others(9): Show | 59 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(56): Show |
synonymous_variant | LOW | c.3030C>T | p.Ser1010Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/36 | 3067/6913 | 3030/5778 | 1010/1925 | chr3 | 129572656 | ||
| chr3:129572908
|
T | C | 39 | a0001c0013a0001c0048a0001c0069others(36): Show | 187 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
synonymous_variant | LOW | c.2871A>G | p.Pro957Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/36 | 2908/6913 | 2871/5778 | 957/1925 | chr3 | 129572908 | ||
| chr3:129573602
|
C | T | 3 | a0009c0032a0009c0033a0017c0058 | 3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.2829G>A | p.Val943Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/36 | 2866/6913 | 2829/5778 | 943/1925 | chr3 | 129573602 | ||
| chr3:129573719
|
G | A | 1 | a0002c0012 | 6 | HG01496.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.2712C>T | p.Asp904Asp | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/36 | 2749/6913 | 2712/5778 | 904/1925 | chr3 | 129573719 | ||
| chr3:129574348
|
G | A | 1 | a0001c0020 | 3 | HG04184.hp1 HG04199.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.2673C>T | p.Pro891Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2710/6913 | 2673/5778 | 891/1925 | chr3 | 129574348 | ||
| chr3:129578380
|
C | G | 23 | a0001c0011a0001c0013a0001c0039others(20): Show | 109 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
synonymous_variant | LOW | c.2295G>C | p.Thr765Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/36 | 2332/6913 | 2295/5778 | 765/1925 | chr3 | 129578380 | ||
| chr3:129583612
|
G | A | 8 | a0004c0004a0004c0019a0004c0035others(5): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
synonymous_variant | LOW | c.2196C>T | p.Ser732Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/36 | 2233/6913 | 2196/5778 | 732/1925 | chr3 | 129583612 | ||
| chr3:129584229
|
G | A | 8 | a0004c0004a0004c0019a0004c0035others(5): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
synonymous_variant | LOW | c.2034C>T | p.His678His | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/36 | 2071/6913 | 2034/5778 | 678/1925 | chr3 | 129584229 | ||
| chr3:129584434
|
G | A | 1 | a0003c0018 | 4 | HG02258.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1980C>T | p.Tyr660Tyr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 2017/6913 | 1980/5778 | 660/1925 | chr3 | 129584434 | ||
| chr3:129586195
|
G | A | 1 | a0001c0056 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1698C>T | p.Cys566Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 4/36 | 1735/6913 | 1698/5778 | 566/1925 | chr3 | 129586195 | ||
| chr3:129589366
|
G | A | 14 | a0001c0002a0001c0028a0001c0061others(11): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
synonymous_variant | LOW | c.1473C>T | p.Asn491Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/36 | 1510/6913 | 1473/5778 | 491/1925 | chr3 | 129589366 | ||
| chr3:129605350
|
A | G | 65 | a0001c0001a0001c0002a0001c0011others(62): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
synonymous_variant | LOW | c.1290T>C | p.Cys430Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 1327/6913 | 1290/5778 | 430/1925 | chr3 | 129605350 | ||
| chr3:129605893
|
C | T | 1 | a0028c0031 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.747G>A | p.Leu249Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 784/6913 | 747/5778 | 249/1925 | chr3 | 129605893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129555225
|
G | A | 4 | a0003c0018t0005a0009c0032t0005a0009c0033t0005others(1): Show | 7 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1087C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 1087 | chr3 | 129555225 | |||||
| chr3:129555268
|
C | A | 1 | a0001c0002t0012 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 1044 | chr3 | 129555268 | |||||
| chr3:129555357
|
C | T | 1 | a0002c0015t0006 | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*955G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 955 | chr3 | 129555357 | |||||
| chr3:129555372
|
C | T | 3 | a0002c0015t0006a0002c0050t0009a0018c0057t0009 | 7 | HG00735.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*940G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 940 | chr3 | 129555372 | |||||
| chr3:129555520
|
G | A | 27 | a0001c0002t0002a0001c0002t0012a0001c0039t0002others(24): Show | 100 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*792C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 792 | chr3 | 129555520 | |||||
| chr3:129555613
|
C | T | 12 | a0002c0017t0004a0002c0017t0007a0003c0008t0004others(9): Show | 33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*699G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 699 | chr3 | 129555613 | |||||
| chr3:129555640
|
C | T | 1 | a0001c0001t0013 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 672 | chr3 | 129555640 | |||||
| chr3:129555731
|
G | A | 1 | a0002c0017t0007 | 3 | HG00140.hp1 HG00738.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 581 | chr3 | 129555731 | |||||
| chr3:129555812
|
C | T | 28 | a0001c0002t0002a0001c0002t0012a0001c0039t0002others(25): Show | 102 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*500G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 500 | chr3 | 129555812 | |||||
| chr3:129555971
|
G | A | 25 | a0001c0013t0003a0002c0003t0003a0002c0009t0003others(22): Show | 102 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*341C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 341 | chr3 | 129555971 | |||||
| chr3:129556035
|
C | T | 1 | a0001c0001t0008 | 3 | HG00639.hp1 HG02735.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 277 | chr3 | 129556035 | |||||
| chr3:129556046
|
G | A | 1 | a0017c0058t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 266 | chr3 | 129556046 | |||||
| chr3:129556093
|
A | G | 15 | a0002c0015t0006a0002c0017t0004a0002c0017t0007others(12): Show | 40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 219 | chr3 | 129556093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129556455
|
G | C | 1 | a0002c0012t0001g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5662-27C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556455 | ||||||
| chr3:129556509
|
C | T | 3 | a0003c0014t0004g0288a0003c0014t0004g0292a0007c0021t0004g0069 | 3 | HG02723.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5662-81G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556509 | ||||||
| chr3:129556560
|
C | A | 33 | a0002c0015t0006g0117a0002c0015t0006g0118a0002c0015t0006g0119others(30): Show | 40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.5661+57G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556560 | ||||||
| chr3:129556712
|
G | A | 1 | a0002c0003t0003g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5587-21C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556712 | ||||||
| chr3:129556776
|
T | C | 88 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(85): Show | 106 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.5587-85A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556776 | ||||||
| chr3:129556837
|
A | G | 8 | a0002c0003t0001g0230a0004c0004t0001g0056a0004c0004t0001g0241others(5): Show | 9 | HG00408.hp2 HG00621.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.5587-146T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556837 | ||||||
| chr3:129556903
|
C | T | 53 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(50): Show | 63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.5586+180G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556903 | ||||||
| chr3:129557065
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5586+18C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129557065 | ||||||
| chr3:129557070
|
C | T | 1 | a0002c0003t0003g0046 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.5586+13G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129557070 | ||||||
| chr3:129557270
|
C | G | 5 | a0002c0015t0006g0117a0002c0015t0006g0118a0002c0015t0006g0119others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5446-47G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557270 | ||||||
| chr3:129557270
|
C | T | 1 | a0002c0005t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5446-47G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557270 | ||||||
| chr3:129557400
|
G | T | 1 | a0001c0002t0002g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5446-177C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557400 | ||||||
| chr3:129557425
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0162 | 3 | HG01106.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5446-202G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557425 | ||||||
| chr3:129557487
|
A | AG | 193 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(190): Show | 257 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.5446-265dupC | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557487 | ||||||
| chr3:129557502
|
G | C | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5446-279C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557502 | ||||||
| chr3:129557533
|
A | G | 3 | a0004c0004t0001g0019a0004c0004t0001g0248a0004c0004t0001g0251 | 5 | HG02015.hp1 HG04228.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.5446-310T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557533 | ||||||
| chr3:129557569
|
T | C | 27 | a0002c0017t0004g0275a0002c0017t0007g0033a0002c0017t0007g0143others(24): Show | 35 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.5446-346A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557569 | ||||||
| chr3:129557643
|
C | T | 42 | a0001c0013t0003g0014a0001c0013t0003g0125a0002c0003t0003g0001others(39): Show | 63 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.5446-420G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557643 | ||||||
| chr3:129557751
|
C | T | 1 | a0008c0022t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5446-528G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557751 | ||||||
| chr3:129557758
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0256 | 2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.5446-535G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557758 | ||||||
| chr3:129558098
|
T | C | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5445+330A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558098 | ||||||
| chr3:129558149
|
C | T | 2 | a0001c0002t0002g0079a0001c0002t0002g0084 | 2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.5445+279G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558149 | ||||||
| chr3:129558303
|
A | C | 92 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(89): Show | 112 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.5445+125T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558303 | ||||||
| chr3:129558638
|
T | C | 29 | a0002c0017t0004g0275a0002c0017t0007g0033a0002c0017t0007g0143others(26): Show | 37 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.5298-63A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129558638 | ||||||
| chr3:129558875
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.5298-300C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129558875 | ||||||
| chr3:129559098
|
G | A | 1 | a0005c0016t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5297+522C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559098 | ||||||
| chr3:129559149
|
C | T | 26 | a0002c0017t0004g0275a0002c0017t0007g0033a0002c0017t0007g0143others(23): Show | 33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.5297+471G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559149 | ||||||
| chr3:129559339
|
A | G | 92 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(89): Show | 112 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.5297+281T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559339 | ||||||
| chr3:129559358
|
G | C | 3 | a0004c0004t0001g0193a0004c0004t0001g0194a0015c0027t0001g0195 | 3 | NA18952.hp2 NA18973.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.5297+262C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559358 | ||||||
| chr3:129559462
|
A | G | 1 | a0029c0046t0001g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5297+158T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559462 | ||||||
| chr3:129559603
|
GC | G | 52 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0068others(49): Show | 63 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.5297+16delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559603 | ||||||
| chr3:129559823
|
C | T | 2 | a0002c0050t0009g0120a0018c0057t0009g0286 | 2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5134-40G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559823 | ||||||
| chr3:129559917
|
C | T | 3 | a0001c0001t0001g0295a0001c0002t0002g0107a0001c0013t0003g0125 | 3 | HG01167.hp2 HG03688.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.5134-134G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559917 | ||||||
| chr3:129559950
|
G | A | 5 | a0002c0015t0006g0117a0002c0015t0006g0118a0002c0015t0006g0119others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5134-167C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559950 | ||||||
| chr3:129560057
|
C | T | 2 | a0002c0050t0009g0120a0018c0057t0009g0286 | 2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5133+273G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560057 | ||||||
| chr3:129560121
|
A | G | 1 | a0004c0004t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5133+209T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560121 | ||||||
| chr3:129560188
|
T | G | 1 | a0003c0008t0004g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5133+142A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560188 | ||||||
| chr3:129560190
|
C | T | 1 | a0002c0005t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5133+140G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560190 | ||||||
| chr3:129560235
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5133+95G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560235 | ||||||
| chr3:129560238
|
G | A | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5133+92C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560238 | ||||||
| chr3:129560727
|
T | C | 88 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(85): Show | 106 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.4994-4A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560727 | ||||||
| chr3:129560754
|
C | T | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(305): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.4994-31G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560754 | ||||||
| chr3:129560828
|
G | A | 3 | a0001c0011t0001g0015a0001c0056t0001g0259a0020c0037t0001g0257 | 6 | HG02622.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4994-105C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560828 | ||||||
| chr3:129560877
|
G | A | 6 | a0003c0008t0004g0038a0003c0008t0004g0039a0003c0008t0004g0177others(3): Show | 8 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.4994-154C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560877 | ||||||
| chr3:129560930
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4994-207G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560930 | ||||||
| chr3:129560992
|
A | G | 60 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(57): Show | 73 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.4994-269T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560992 | ||||||
| chr3:129561021
|
G | A | 1 | a0006c0023t0001g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4994-298C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561021 | ||||||
| chr3:129561127
|
C | T | 5 | a0002c0015t0006g0117a0002c0015t0006g0118a0002c0015t0006g0119others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4994-404G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561127 | ||||||
| chr3:129561313
|
G | A | 1 | a0003c0051t0004g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4993+333C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561313 | ||||||
| chr3:129561418
|
C | T | 27 | a0002c0017t0004g0275a0002c0017t0007g0033a0002c0017t0007g0143others(24): Show | 34 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.4993+228G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561418 | ||||||
| chr3:129561639
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19077.hp2 | splice_region_variant&intron_variant | LOW | c.4993+7C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561639 | ||||||
| chr3:129561730
|
G | A | 1 | a0003c0008t0004g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4930-21C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 28/35 | chr3 | 129561730 | ||||||
| chr3:129561782
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4929+18G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 28/35 | chr3 | 129561782 | ||||||
| chr3:129561967
|
G | C | 1 | a0002c0005t0001g0277 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4826-64C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129561967 | ||||||
| chr3:129562101
|
C | T | 32 | a0002c0017t0004g0275a0002c0017t0007g0033a0002c0017t0007g0143others(29): Show | 40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.4826-198G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562101 | ||||||
| chr3:129562163
|
A | G | 5 | a0002c0015t0006g0117a0002c0015t0006g0118a0002c0015t0006g0119others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4826-260T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562163 | ||||||
| chr3:129562194
|
C | T | 1 | a0002c0009t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4826-291G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562194 | ||||||
| chr3:129562236
|
C | T | 1 | a0004c0004t0001g0251 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4826-333G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562236 | ||||||
| chr3:129562245
|
GCTCACAC others(4): Show |
G | 53 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(50): Show | 63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.4826-353_4826-343d others(13): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562245 | ||||||
| chr3:129562370
|
TGTG | T | 53 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(50): Show | 63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.4825+414_4825+416d others(5): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562370 | ||||||
| chr3:129562378
|
T | C | 1 | a0001c0056t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4825+409A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562378 | ||||||
| chr3:129562595
|
C | T | 30 | a0002c0017t0004g0275a0002c0050t0009g0120a0003c0008t0004g0017others(27): Show | 37 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4825+192G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562595 | ||||||
| chr3:129562615
|
G | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0142others(27): Show | 40 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.4825+172C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562615 | ||||||
| chr3:129563023
|
G | C | 44 | a0001c0069t0011g0306a0002c0005t0001g0287a0002c0017t0004g0275others(41): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.4668+71C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/35 | chr3 | 129563023 | ||||||
| chr3:129563270
|
G | C | 1 | a0002c0012t0001g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4522-30C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563270 | ||||||
| chr3:129563294
|
T | C | 211 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(208): Show | 279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.4522-54A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563294 | ||||||
| chr3:129563295
|
G | A | 30 | a0002c0005t0001g0155a0003c0007t0001g0009a0003c0007t0001g0026others(27): Show | 43 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.4522-55C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563295 | ||||||
| chr3:129563510
|
C | T | 55 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(52): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4522-270G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563510 | ||||||
| chr3:129563579
|
C | T | 2 | a0008c0022t0001g0060a0008c0022t0001g0061 | 2 | HG01516.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.4522-339G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563579 | ||||||
| chr3:129563697
|
A | G | 54 | a0001c0001t0008g0173a0001c0069t0011g0306a0002c0006t0001g0007others(51): Show | 68 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.4522-457T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563697 | ||||||
| chr3:129563784
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4522-544T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563784 | ||||||
| chr3:129564024
|
T | C | 1 | a0002c0006t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4522-784A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564024 | ||||||
| chr3:129564027
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4522-787C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564027 | ||||||
| chr3:129564125
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4522-885G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564125 | ||||||
| chr3:129564134
|
C | T | 81 | a0001c0069t0011g0306a0002c0006t0001g0007a0002c0006t0001g0269others(78): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.4522-894G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564134 | ||||||
| chr3:129564269
|
G | A | 2 | a0007c0021t0002g0023a0007c0021t0004g0069 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4522-1029C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564269 | ||||||
| chr3:129564416
|
C | T | 4 | a0002c0003t0003g0046a0002c0003t0003g0211a0002c0003t0003g0233others(1): Show | 5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.4521+924G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564416 | ||||||
| chr3:129564510
|
T | G | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4521+830A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564510 | ||||||
| chr3:129564606
|
C | T | 3 | a0001c0002t0002g0008a0001c0002t0002g0097a0027c0063t0002g0074 | 6 | HG02080.hp2 HG02083.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.4521+734G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564606 | ||||||
| chr3:129564698
|
G | A | 8 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0006t0001g0285others(5): Show | 11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.4521+642C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564698 | ||||||
| chr3:129564710
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4521+630A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564710 | ||||||
| chr3:129564766
|
C | T | 4 | a0002c0003t0003g0046a0002c0003t0003g0211a0002c0003t0003g0233others(1): Show | 5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.4521+574G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564766 | ||||||
| chr3:129564769
|
A | T | 1 | a0002c0070t0011g0305 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4521+571T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564769 | ||||||
| chr3:129564783
|
C | T | 55 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(52): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4521+557G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564783 | ||||||
| chr3:129564832
|
A | G | 4 | a0002c0049t0001g0280a0005c0016t0001g0022a0005c0016t0001g0307others(1): Show | 6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4521+508T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564832 | ||||||
| chr3:129564839
|
G | T | 20 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(17): Show | 24 | HG00408.hp2 HG02015.hp1 HG02148.hp2 others(21): Show |
intron_variant | MODIFIER | c.4521+501C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564839 | ||||||
| chr3:129564922
|
G | A | 89 | a0001c0069t0011g0306a0002c0006t0001g0007a0002c0006t0001g0010others(86): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4521+418C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564922 | ||||||
| chr3:129565060
|
G | A | 1 | a0002c0005t0001g0276 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4521+280C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565060 | ||||||
| chr3:129565217
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0064 | 6 | NA18945.hp1 NA18947.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.4521+123G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565217 | ||||||
| chr3:129565270
|
G | A | 1 | a0001c0020t0001g0166 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4521+70C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565270 | ||||||
| chr3:129565284
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4521+56C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565284 | ||||||
| chr3:129565307
|
G | A | 37 | a0002c0006t0001g0007a0002c0006t0001g0269a0002c0006t0001g0289others(34): Show | 46 | HG00408.hp2 HG00639.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.4521+33C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565307 | ||||||
| chr3:129565546
|
C | T | 1 | a0015c0027t0001g0201 | 1 | NA18974.hp2 | splice_region_variant&intron_variant | LOW | c.4323-8G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565546 | ||||||
| chr3:129565572
|
G | T | 40 | a0001c0069t0011g0306a0002c0070t0011g0305a0003c0007t0001g0009others(37): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4323-34C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565572 | ||||||
| chr3:129565619
|
C | G | 4 | a0002c0049t0001g0280a0005c0016t0001g0022a0005c0016t0001g0307others(1): Show | 6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4323-81G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565619 | ||||||
| chr3:129565711
|
C | G | 55 | a0001c0001t0001g0160a0001c0002t0002g0005a0001c0002t0002g0008others(52): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4323-173G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565711 | ||||||
| chr3:129565794
|
A | G | 91 | a0001c0069t0011g0306a0002c0006t0001g0007a0002c0006t0001g0010others(88): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4322+93T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565794 | ||||||
| chr3:129566138
|
C | T | 1 | a0001c0020t0001g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4192-121G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566138 | ||||||
| chr3:129566156
|
C | T | 1 | a0001c0020t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4192-139G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566156 | ||||||
| chr3:129566332
|
G | A | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4191+195C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566332 | ||||||
| chr3:129566425
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0162 | 3 | HG01106.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4191+102C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566425 | ||||||
| chr3:129566433
|
G | A | 1 | a0001c0002t0002g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4191+94C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566433 | ||||||
| chr3:129566480
|
G | A | 1 | a0004c0004t0001g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4191+47C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566480 | ||||||
| chr3:129566734
|
A | C | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4087-103T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566734 | ||||||
| chr3:129566744
|
G | A | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4087-113C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566744 | ||||||
| chr3:129566757
|
C | T | 1 | a0001c0002t0002g0101 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4087-126G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566757 | ||||||
| chr3:129567060
|
G | GGGCA | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4086+428_4087-430d others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567060 | ||||||
| chr3:129567118
|
G | T | 1 | a0028c0031t0002g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4086+374C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567118 | ||||||
| chr3:129567205
|
GC | G | 45 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(42): Show | 57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4086+286delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567205 | ||||||
| chr3:129567366
|
C | T | 3 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0006t0001g0285 | 6 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.4086+126G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567366 | ||||||
| chr3:129567484
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.4086+8C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567484 | ||||||
| chr3:129567688
|
C | A | 126 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0069t0011g0306others(123): Show | 172 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.3973+10G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/35 | chr3 | 129567688 | ||||||
| chr3:129567810
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.3866-5C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129567810 | ||||||
| chr3:129567983
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3866-178G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129567983 | ||||||
| chr3:129568032
|
C | T | 1 | a0003c0051t0004g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3866-227G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568032 | ||||||
| chr3:129568033
|
G | A | 8 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0006t0001g0285others(5): Show | 11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3866-228C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568033 | ||||||
| chr3:129568088
|
C | G | 1 | a0028c0031t0002g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-283G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568088 | ||||||
| chr3:129568089
|
G | T | 1 | a0028c0031t0002g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-284C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568089 | ||||||
| chr3:129568091
|
T | A | 1 | a0028c0031t0002g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-286A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568091 | ||||||
| chr3:129568161
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(48): Show | 69 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.3866-356T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568161 | ||||||
| chr3:129568333
|
A | G | 1 | a0001c0002t0002g0088 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3866-528T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568333 | ||||||
| chr3:129568506
|
C | T | 1 | a0015c0027t0001g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3866-701G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568506 | ||||||
| chr3:129568630
|
C | T | 88 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0069t0011g0306others(85): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3866-825G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568630 | ||||||
| chr3:129568714
|
A | G | 4 | a0002c0049t0001g0280a0005c0016t0001g0022a0005c0016t0001g0307others(1): Show | 6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3866-909T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568714 | ||||||
| chr3:129568733
|
G | C | 1 | a0003c0008t0004g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3866-928C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568733 | ||||||
| chr3:129569173
|
A | T | 1 | a0003c0010t0001g0020 | 3 | HG02602.hp2 HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3865+670T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569173 | ||||||
| chr3:129569194
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+649A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569194 | ||||||
| chr3:129569195
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+648T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569195 | ||||||
| chr3:129569197
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+646A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569197 | ||||||
| chr3:129569256
|
A | AAC | 135 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0048t0002g0134others(132): Show | 186 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.3865+585_3865+586d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569256 | ||||||
| chr3:129569258
|
C | CAT | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3865+584_3865+585i others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569258 | ||||||
| chr3:129569285
|
G | A | 9 | a0003c0008t0004g0038a0003c0008t0004g0039a0003c0008t0004g0177others(6): Show | 11 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.3865+558C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569285 | ||||||
| chr3:129569463
|
T | C | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3865+380A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569463 | ||||||
| chr3:129569562
|
A | G | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3865+281T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569562 | ||||||
| chr3:129569632
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0199 | 4 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+211G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569632 | ||||||
| chr3:129569707
|
C | A | 1 | a0001c0020t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3865+136G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569707 | ||||||
| chr3:129569726
|
CT | C | 4 | a0002c0003t0003g0046a0002c0003t0003g0211a0002c0003t0003g0233others(1): Show | 5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3865+116delA | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569726 | ||||||
| chr3:129569805
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3865+38G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569805 | ||||||
| chr3:129570008
|
A | G | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3751-51T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570008 | ||||||
| chr3:129570215
|
G | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0137a0001c0001t0001g0157others(6): Show | 10 | HG00558.hp2 HG01934.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3751-258C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570215 | ||||||
| chr3:129570236
|
G | A | 1 | a0002c0009t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3751-279C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570236 | ||||||
| chr3:129570247
|
C | T | 49 | a0002c0006t0001g0007a0002c0006t0001g0010a0002c0006t0001g0123others(46): Show | 63 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.3751-290G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570247 | ||||||
| chr3:129570415
|
T | C | 86 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0048t0002g0134others(83): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.3750+371A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570415 | ||||||
| chr3:129570419
|
C | CA | 46 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0048t0002g0134others(43): Show | 67 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3750+366dupT | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570419 | ||||||
| chr3:129570458
|
T | A | 1 | a0002c0003t0003g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3750+328A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570458 | ||||||
| chr3:129570504
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3750+282G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570504 | ||||||
| chr3:129570752
|
A | G | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3750+34T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570752 | ||||||
| chr3:129570774
|
C | T | 1 | a0001c0039t0002g0231 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3750+12G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570774 | ||||||
| chr3:129570988
|
A | G | 192 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(189): Show | 254 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.3600+52T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129570988 | ||||||
| chr3:129571002
|
C | T | 1 | a0004c0019t0004g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3600+38G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129571002 | ||||||
| chr3:129571018
|
C | T | 1 | a0003c0018t0005g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3600+22G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129571018 | ||||||
| chr3:129571344
|
T | C | 88 | a0001c0013t0003g0014a0001c0013t0003g0125a0001c0048t0002g0134others(85): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3337-41A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571344 | ||||||
| chr3:129571425
|
G | A | 1 | a0003c0008t0004g0017 | 3 | HG01123.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.3336+84C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571425 | ||||||
| chr3:129571484
|
C | T | 1 | a0004c0004t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3336+25G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571484 | ||||||
| chr3:129571876
|
T | C | 1 | a0005c0016t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3078-32A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571876 | ||||||
| chr3:129571898
|
G | A | 1 | a0006c0040t0004g0262 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3078-54C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571898 | ||||||
| chr3:129571934
|
A | G | 1 | a0005c0016t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3078-90T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571934 | ||||||
| chr3:129571941
|
C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3078-97G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571941 | ||||||
| chr3:129571981
|
C | T | 1 | a0001c0002t0002g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3078-137G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571981 | ||||||
| chr3:129572013
|
C | T | 1 | a0003c0010t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3078-169G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572013 | ||||||
| chr3:129572025
|
G | T | 1 | a0004c0004t0001g0253 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3078-181C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572025 | ||||||
| chr3:129572089
|
GTC | G | 54 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(51): Show | 65 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.3078-247_3078-246d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572089 | ||||||
| chr3:129572302
|
G | A | 1 | a0002c0012t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3077+307C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572302 | ||||||
| chr3:129572587
|
T | C | 1 | a0001c0002t0002g0091 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3077+22A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572587 | ||||||
| chr3:129572800
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2937+42G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/35 | chr3 | 129572800 | ||||||
| chr3:129573025
|
C | T | 53 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(50): Show | 64 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2838-84G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573025 | ||||||
| chr3:129573093
|
A | G | 2 | a0002c0050t0009g0120a0018c0057t0009g0286 | 2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2838-152T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573093 | ||||||
| chr3:129573222
|
C | T | 82 | a0001c0013t0003g0014a0001c0013t0003g0125a0002c0003t0001g0230others(79): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2838-281G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573222 | ||||||
| chr3:129573424
|
C | T | 2 | a0003c0014t0004g0053a0003c0014t0004g0284 | 3 | HG02647.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2837+170G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573424 | ||||||
| chr3:129573520
|
A | G | 1 | a0004c0004t0001g0253 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2837+74T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573520 | ||||||
| chr3:129573521
|
G | A | 1 | a0004c0004t0001g0253 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2837+73C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573521 | ||||||
| chr3:129573578
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2837+16G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573578 | ||||||
| chr3:129573843
|
C | G | 1 | a0001c0002t0002g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2686-98G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129573843 | ||||||
| chr3:129574034
|
T | C | 1 | a0002c0003t0003g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2686-289A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574034 | ||||||
| chr3:129574105
|
C | T | 17 | a0003c0007t0001g0009a0003c0007t0001g0026a0003c0007t0001g0027others(14): Show | 25 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.2685+231G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574105 | ||||||
| chr3:129574181
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0064 | 6 | NA18945.hp1 NA18947.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+155C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574181 | ||||||
| chr3:129574263
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(162): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2685+73C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574263 | ||||||
| chr3:129574303
|
C | T | 1 | a0003c0007t0001g0026 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2685+33G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574303 | ||||||
| chr3:129574522
|
C | T | 1 | a0013c0054t0003g0220 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2531-32G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574522 | ||||||
| chr3:129574587
|
G | A | 1 | a0001c0045t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2531-97C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574587 | ||||||
| chr3:129574764
|
A | G | 35 | a0002c0006t0001g0007a0002c0006t0001g0269a0002c0006t0001g0289others(32): Show | 44 | HG00408.hp2 HG00639.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.2531-274T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574764 | ||||||
| chr3:129574804
|
C | T | 2 | a0001c0002t0002g0112a0004c0019t0004g0249 | 2 | HG00639.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2531-314G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574804 | ||||||
| chr3:129574821
|
C | G | 2 | a0001c0002t0002g0071a0001c0002t0002g0081 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2531-331G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574821 | ||||||
| chr3:129574847
|
C | T | 37 | a0001c0069t0011g0306a0002c0006t0001g0010a0002c0006t0001g0123others(34): Show | 44 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2531-357G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574847 | ||||||
| chr3:129574853
|
C | A | 1 | a0001c0002t0002g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2531-363G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574853 | ||||||
| chr3:129574946
|
C | T | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-456G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574946 | ||||||
| chr3:129574996
|
G | A | 24 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(21): Show | 28 | HG00639.hp2 HG01981.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.2530+473C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574996 | ||||||
| chr3:129575106
|
A | C | 14 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0158others(11): Show | 20 | HG00597.hp1 HG00609.hp2 HG03490.hp1 others(17): Show |
intron_variant | MODIFIER | c.2530+363T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575106 | ||||||
| chr3:129575130
|
T | C | 59 | a0001c0069t0011g0306a0002c0006t0001g0007a0002c0006t0001g0010others(56): Show | 76 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(73): Show |
intron_variant | MODIFIER | c.2530+339A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575130 | ||||||
| chr3:129575240
|
T | A | 1 | a0001c0045t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2530+229A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575240 | ||||||
| chr3:129575273
|
CTA | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(89): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.2530+194_2530+195d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575273 | ||||||
| chr3:129575401
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02280.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2530+68C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575401 | ||||||
| chr3:129575451
|
G | C | 39 | a0001c0069t0011g0306a0002c0006t0001g0010a0002c0006t0001g0123others(36): Show | 46 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2530+18C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575451 | ||||||
| chr3:129575613
|
C | T | 73 | a0001c0011t0001g0015a0001c0011t0001g0212a0001c0011t0001g0215others(70): Show | 106 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-51G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575613 | ||||||
| chr3:129575615
|
G | A | 1 | a0003c0007t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2437-53C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575615 | ||||||
| chr3:129575719
|
C | T | 1 | a0004c0004t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2436+47G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575719 | ||||||
| chr3:129575725
|
G | A | 62 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(59): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2436+41C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575725 | ||||||
| chr3:129575880
|
C | T | 1 | a0001c0001t0001g0021 | 3 | HG00323.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2347-25G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129575880 | ||||||
| chr3:129575998
|
G | A | 2 | a0001c0002t0002g0079a0001c0002t0002g0084 | 2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2347-143C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129575998 | ||||||
| chr3:129576170
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2347-315G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576170 | ||||||
| chr3:129576244
|
G | A | 3 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0006t0001g0285 | 6 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2347-389C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576244 | ||||||
| chr3:129576272
|
G | A | 1 | a0018c0057t0009g0286 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2347-417C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576272 | ||||||
| chr3:129576289
|
T | C | 1 | a0003c0014t0004g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2347-434A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576289 | ||||||
| chr3:129576356
|
A | G | 1 | a0002c0003t0003g0301 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2347-501T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576356 | ||||||
| chr3:129576592
|
A | T | 1 | a0001c0002t0002g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2347-737T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576592 | ||||||
| chr3:129576622
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2347-767A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576622 | ||||||
| chr3:129576687
|
G | A | 1 | a0001c0002t0002g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2347-832C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576687 | ||||||
| chr3:129576776
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG00099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2347-921G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576776 | ||||||
| chr3:129576811
|
A | G | 2 | a0007c0021t0002g0023a0007c0021t0004g0069 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2347-956T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576811 | ||||||
| chr3:129576863
|
C | T | 1 | a0030c0060t0002g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2347-1008G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576863 | ||||||
| chr3:129577137
|
CCT | C | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2346+1190_2346+119 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577137 | ||||||
| chr3:129577177
|
C | T | 115 | a0001c0011t0001g0015a0001c0011t0001g0212a0001c0011t0001g0215others(112): Show | 157 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.2346+1152G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577177 | ||||||
| chr3:129577224
|
G | A | 1 | a0004c0004t0001g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2346+1105C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577224 | ||||||
| chr3:129577233
|
G | A | 1 | a0004c0004t0001g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2346+1096C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577233 | ||||||
| chr3:129577635
|
A | G | 1 | a0001c0002t0002g0073 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2346+694T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577635 | ||||||
| chr3:129577913
|
G | T | 42 | a0001c0069t0011g0306a0002c0006t0001g0010a0002c0006t0001g0123others(39): Show | 51 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.2346+416C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577913 | ||||||
| chr3:129577939
|
G | A | 60 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(57): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2346+390C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577939 | ||||||
| chr3:129578004
|
A | G | 76 | a0001c0011t0001g0015a0001c0011t0001g0212a0001c0011t0001g0215others(73): Show | 109 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2346+325T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578004 | ||||||
| chr3:129578035
|
C | T | 1 | a0002c0005t0001g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2346+294G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578035 | ||||||
| chr3:129578152
|
G | A | 2 | a0007c0021t0002g0023a0007c0021t0004g0069 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2346+177C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578152 | ||||||
| chr3:129578169
|
G | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(304): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.2346+160C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578169 | ||||||
| chr3:129578554
|
T | C | 1 | a0005c0016t0001g0022 | 3 | HG02109.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2242-121A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578554 | ||||||
| chr3:129578635
|
C | T | 60 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(57): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2242-202G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578635 | ||||||
| chr3:129578750
|
A | G | 29 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(26): Show | 33 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.2242-317T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578750 | ||||||
| chr3:129578834
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2242-401C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578834 | ||||||
| chr3:129579049
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2242-616G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579049 | ||||||
| chr3:129579232
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2242-799T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579232 | ||||||
| chr3:129579255
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2242-822G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579255 | ||||||
| chr3:129579263
|
A | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01106.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2242-830T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579263 | ||||||
| chr3:129579286
|
G | A | 35 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0015t0006g0117others(32): Show | 42 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.2242-853C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579286 | ||||||
| chr3:129579320
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2242-887G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579320 | ||||||
| chr3:129579466
|
G | A | 1 | a0002c0050t0009g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2242-1033C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579466 | ||||||
| chr3:129579510
|
A | C | 1 | a0009c0032t0005g0268 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2242-1077T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579510 | ||||||
| chr3:129579577
|
C | T | 2 | a0005c0016t0001g0022a0005c0016t0001g0308 | 4 | HG02109.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-1144G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579577 | ||||||
| chr3:129579702
|
T | A | 1 | a0004c0004t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2242-1269A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579702 | ||||||
| chr3:129579843
|
C | T | 73 | a0001c0011t0001g0015a0001c0011t0001g0212a0001c0011t0001g0215others(70): Show | 105 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2242-1410G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579843 | ||||||
| chr3:129579950
|
A | G | 1 | a0004c0004t0001g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2242-1517T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579950 | ||||||
| chr3:129580151
|
G | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(229): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2242-1718C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580151 | ||||||
| chr3:129580182
|
C | G | 4 | a0001c0002t0002g0079a0001c0002t0002g0084a0001c0002t0002g0205others(1): Show | 4 | HG00423.hp1 NA18963.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-1749G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580182 | ||||||
| chr3:129580235
|
G | A | 2 | a0001c0002t0002g0008a0001c0002t0002g0097 | 5 | HG02080.hp2 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242-1802C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580235 | ||||||
| chr3:129580236
|
G | GC | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2242-1804dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580236 | ||||||
| chr3:129580422
|
G | A | 12 | a0001c0001t0001g0063a0001c0001t0001g0264a0003c0010t0001g0020others(9): Show | 15 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242-1989C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580422 | ||||||
| chr3:129580438
|
T | C | 108 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(105): Show | 146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2242-2005A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580438 | ||||||
| chr3:129580560
|
G | C | 1 | a0004c0004t0001g0299 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2242-2127C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580560 | ||||||
| chr3:129580715
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(277): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2242-2282A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580715 | ||||||
| chr3:129580745
|
G | A | 5 | a0004c0004t0001g0049a0004c0004t0001g0243a0015c0027t0001g0201others(2): Show | 6 | NA18974.hp2 NA18977.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-2312C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580745 | ||||||
| chr3:129581039
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2241+2528A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581039 | ||||||
| chr3:129581039
|
T | G | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+2528A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581039 | ||||||
| chr3:129581055
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2241+2512C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581055 | ||||||
| chr3:129581316
|
C | A | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+2251G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581316 | ||||||
| chr3:129581333
|
C | T | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+2234G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581333 | ||||||
| chr3:129581446
|
C | T | 2 | a0002c0003t0003g0235a0002c0005t0001g0287 | 2 | HG01884.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2241+2121G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581446 | ||||||
| chr3:129581448
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(93): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.2241+2119T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581448 | ||||||
| chr3:129581464
|
AGAAATCC others(7): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2241+2089_2241+210 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581464 | ||||||
| chr3:129581733
|
T | C | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1834A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581733 | ||||||
| chr3:129581760
|
G | A | 1 | a0019c0055t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2241+1807C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581760 | ||||||
| chr3:129581820
|
C | T | 1 | a0019c0055t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2241+1747G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581820 | ||||||
| chr3:129581864
|
C | A | 108 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(105): Show | 146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2241+1703G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581864 | ||||||
| chr3:129581909
|
A | G | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1658T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581909 | ||||||
| chr3:129581990
|
G | GGAGCAGG others(19): Show |
1 | a0002c0003t0003g0211 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2241+1551_2241+157 others(30): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581990 | ||||||
| chr3:129581997
|
G | A | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+1570C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581997 | ||||||
| chr3:129582024
|
A | G | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1543T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582024 | ||||||
| chr3:129582056
|
G | A | 1 | a0004c0004t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2241+1511C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582056 | ||||||
| chr3:129582090
|
C | T | 75 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(72): Show | 107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1477G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582090 | ||||||
| chr3:129582315
|
A | G | 1 | a0001c0047t0002g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2241+1252T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582315 | ||||||
| chr3:129582428
|
T | C | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1139A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582428 | ||||||
| chr3:129582522
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0256 | 2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2241+1045G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582522 | ||||||
| chr3:129582543
|
G | C | 2 | a0007c0021t0002g0023a0007c0021t0004g0069 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2241+1024C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582543 | ||||||
| chr3:129582575
|
CCCTGGCA others(7): Show |
C | 1 | a0001c0047t0002g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2241+978_2241+991d others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582575 | ||||||
| chr3:129582608
|
C | T | 1 | a0003c0008t0004g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2241+959G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582608 | ||||||
| chr3:129582705
|
G | A | 1 | a0001c0064t0001g0093 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2241+862C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582705 | ||||||
| chr3:129582726
|
A | G | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+841T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582726 | ||||||
| chr3:129583031
|
G | A | 76 | a0001c0001t0001g0063a0001c0001t0001g0187a0001c0001t0001g0264others(73): Show | 108 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2241+536C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583031 | ||||||
| chr3:129583102
|
T | G | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+465A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583102 | ||||||
| chr3:129583277
|
T | C | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+290A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583277 | ||||||
| chr3:129583316
|
G | A | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+251C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583316 | ||||||
| chr3:129583418
|
C | T | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+149G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583418 | ||||||
| chr3:129583424
|
G | A | 1 | a0009c0033t0005g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2241+143C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583424 | ||||||
| chr3:129583786
|
G | A | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2139-117C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129583786 | ||||||
| chr3:129584029
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2138+96A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584029 | ||||||
| chr3:129584049
|
C | G | 2 | a0006c0023t0001g0138a0006c0023t0001g0144 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2138+76G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584049 | ||||||
| chr3:129584055
|
A | G | 1 | a0002c0005t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2138+70T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584055 | ||||||
| chr3:129584354
|
T | C | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(303): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.2029+31A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/35 | chr3 | 129584354 | ||||||
| chr3:129584355
|
G | A | 1 | a0002c0005t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2029+30C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/35 | chr3 | 129584355 | ||||||
| chr3:129584593
|
T | G | 132 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0002t0002g0005others(129): Show | 179 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1852-31A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584593 | ||||||
| chr3:129584645
|
C | G | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1852-83G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584645 | ||||||
| chr3:129584660
|
T | A | 2 | a0009c0032t0005g0268a0009c0033t0005g0267 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1852-98A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584660 | ||||||
| chr3:129584729
|
T | A | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1852-167A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584729 | ||||||
| chr3:129584742
|
T | G | 1 | a0002c0015t0006g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1852-180A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584742 | ||||||
| chr3:129584901
|
G | A | 165 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0002t0002g0005others(162): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1852-339C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584901 | ||||||
| chr3:129584989
|
C | T | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-427G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584989 | ||||||
| chr3:129585081
|
G | A | 1 | a0001c0002t0002g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1852-519C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585081 | ||||||
| chr3:129585139
|
G | A | 1 | a0002c0012t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1852-577C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585139 | ||||||
| chr3:129585207
|
A | G | 7 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0015t0006g0117others(4): Show | 10 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1852-645T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585207 | ||||||
| chr3:129585380
|
G | A | 2 | a0001c0001t0001g0153a0001c0045t0001g0149 | 2 | HG01106.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1851+572C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585380 | ||||||
| chr3:129585407
|
G | A | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1851+545C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585407 | ||||||
| chr3:129585463
|
G | A | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1851+489C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585463 | ||||||
| chr3:129585472
|
T | C | 47 | a0001c0011t0001g0212a0001c0011t0001g0215a0001c0013t0003g0014others(44): Show | 68 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1851+480A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585472 | ||||||
| chr3:129585502
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1851+450G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585502 | ||||||
| chr3:129585607
|
C | G | 30 | a0004c0004t0001g0019a0004c0004t0001g0049a0004c0004t0001g0056others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1851+345G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585607 | ||||||
| chr3:129586391
|
A | G | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1621-119T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586391 | ||||||
| chr3:129586450
|
A | G | 2 | a0005c0016t0001g0022a0005c0016t0001g0308 | 4 | HG02109.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620+138T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586450 | ||||||
| chr3:129586476
|
G | C | 1 | a0003c0008t0004g0017 | 3 | HG01123.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1620+112C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586476 | ||||||
| chr3:129586527
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1620+61G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586527 | ||||||
| chr3:129586558
|
G | A | 2 | a0001c0001t0001g0184a0001c0045t0001g0149 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1620+30C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586558 | ||||||
| chr3:129586727
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp2 | splice_region_variant&intron_variant | LOW | c.1489-8C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586727 | ||||||
| chr3:129586756
|
T | C | 3 | a0002c0003t0003g0222a0002c0003t0003g0235a0002c0043t0003g0223 | 3 | NA18999.hp2 NA19009.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1489-37A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586756 | ||||||
| chr3:129586779
|
G | A | 1 | a0002c0005t0001g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1489-60C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586779 | ||||||
| chr3:129586863
|
A | C | 1 | a0003c0010t0001g0050 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1489-144T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586863 | ||||||
| chr3:129586989
|
C | T | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-270G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586989 | ||||||
| chr3:129586995
|
C | G | 1 | a0001c0001t0013g0147 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1489-276G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586995 | ||||||
| chr3:129587076
|
T | C | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1489-357A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587076 | ||||||
| chr3:129587189
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1489-470C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587189 | ||||||
| chr3:129587222
|
C | A | 2 | a0003c0010t0001g0020a0003c0010t0001g0265 | 4 | HG02602.hp2 HG03017.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-503G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587222 | ||||||
| chr3:129587222
|
C | G | 69 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0002t0002g0094others(66): Show | 97 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1489-503G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587222 | ||||||
| chr3:129587224
|
G | C | 165 | a0001c0001t0001g0063a0001c0001t0001g0114a0001c0001t0001g0115others(162): Show | 217 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1489-505C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587224 | ||||||
| chr3:129587361
|
G | A | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1489-642C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587361 | ||||||
| chr3:129587366
|
T | C | 1 | a0002c0005t0001g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1489-647A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587366 | ||||||
| chr3:129587437
|
C | A | 69 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(66): Show | 99 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1489-718G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587437 | ||||||
| chr3:129587470
|
G | A | 2 | a0002c0005t0001g0126a0002c0005t0001g0127 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1489-751C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587470 | ||||||
| chr3:129587498
|
T | C | 3 | a0005c0016t0001g0022a0005c0016t0001g0307a0005c0016t0001g0308 | 5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-779A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587498 | ||||||
| chr3:129587648
|
T | C | 2 | a0006c0023t0001g0138a0006c0023t0001g0144 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-929A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587648 | ||||||
| chr3:129587686
|
C | T | 1 | a0004c0004t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1489-967G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587686 | ||||||
| chr3:129587968
|
C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1489-1249G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587968 | ||||||
| chr3:129587971
|
A | AC | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(142): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1489-1253dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587971 | ||||||
| chr3:129588050
|
C | T | 69 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(66): Show | 99 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1488+1301G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588050 | ||||||
| chr3:129588172
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1488+1179T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588172 | ||||||
| chr3:129588277
|
G | A | 1 | a0032c0034t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1488+1074C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588277 | ||||||
| chr3:129588348
|
C | T | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+1003G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588348 | ||||||
| chr3:129588412
|
A | T | 1 | a0001c0002t0002g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1488+939T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588412 | ||||||
| chr3:129588428
|
GC | G | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+922delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588428 | ||||||
| chr3:129588471
|
TGTGA | T | 159 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0002t0002g0005others(156): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1488+876_1488+879d others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588471 | ||||||
| chr3:129588560
|
A | G | 2 | a0006c0023t0001g0138a0006c0023t0001g0144 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1488+791T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588560 | ||||||
| chr3:129588609
|
G | C | 5 | a0002c0005t0001g0287a0002c0006t0001g0007a0002c0006t0001g0269others(2): Show | 9 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+742C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588609 | ||||||
| chr3:129588645
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1488+706C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588645 | ||||||
| chr3:129588658
|
G | A | 1 | a0002c0003t0003g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1488+693C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588658 | ||||||
| chr3:129588803
|
C | T | 68 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(65): Show | 98 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1488+548G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588803 | ||||||
| chr3:129588814
|
C | T | 3 | a0009c0032t0005g0268a0009c0033t0005g0267a0017c0058t0014g0270 | 3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1488+537G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588814 | ||||||
| chr3:129588884
|
G | C | 1 | a0003c0010t0001g0050 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1488+467C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588884 | ||||||
| chr3:129588969
|
G | A | 8 | a0002c0006t0001g0010a0002c0006t0001g0123a0002c0015t0006g0117others(5): Show | 11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1488+382C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588969 | ||||||
| chr3:129589114
|
T | G | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+237A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589114 | ||||||
| chr3:129589149
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(300): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.1488+202A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589149 | ||||||
| chr3:129589253
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(139): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1488+98C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589253 | ||||||
| chr3:129589545
|
C | T | 1 | a0002c0005t0001g0272 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1312-18G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589545 | ||||||
| chr3:129589582
|
G | A | 30 | a0001c0069t0011g0306a0002c0070t0011g0305a0003c0010t0001g0050others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1312-55C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589582 | ||||||
| chr3:129589594
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1312-67C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589594 | ||||||
| chr3:129589654
|
A | C | 30 | a0001c0069t0011g0306a0002c0070t0011g0305a0003c0010t0001g0050others(27): Show | 34 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1312-127T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589654 | ||||||
| chr3:129589874
|
T | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-347A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589874 | ||||||
| chr3:129589900
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0190 | 2 | NA18990.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1312-373C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589900 | ||||||
| chr3:129590041
|
C | A | 1 | a0002c0003t0003g0224 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1312-514G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590041 | ||||||
| chr3:129590062
|
G | T | 1 | a0001c0047t0002g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-535C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590062 | ||||||
| chr3:129590083
|
A | C | 1 | a0002c0003t0003g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1312-556T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590083 | ||||||
| chr3:129590304
|
G | A | 68 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0015others(65): Show | 97 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1312-777C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590304 | ||||||
| chr3:129590304
|
G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(139): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1312-777C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590304 | ||||||
| chr3:129590307
|
CT | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(140): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1312-781delA | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590307 | ||||||
| chr3:129590349
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1312-822C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590349 | ||||||
| chr3:129590420
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(140): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1312-893A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590420 | ||||||
| chr3:129590442
|
C | T | 1 | a0004c0004t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1312-915G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590442 | ||||||
| chr3:129590558
|
C | T | 2 | a0002c0005t0001g0055a0002c0005t0001g0291 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1312-1031G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590558 | ||||||
| chr3:129590607
|
T | C | 1 | a0001c0002t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1312-1080A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590607 | ||||||
| chr3:129590612
|
G | A | 61 | a0001c0001t0001g0063a0001c0001t0001g0264a0001c0011t0001g0212others(58): Show | 84 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1312-1085C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590612 | ||||||
| chr3:129590735
|
C | A | 1 | a0005c0016t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1312-1208G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590735 | ||||||
| chr3:129590746
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1312-1219C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590746 | ||||||
| chr3:129591018
|
C | CAA | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-1492_1312-149 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591018 | ||||||
| chr3:129591044
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1312-1517C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591044 | ||||||
| chr3:129591059
|
T | C | 1 | a0005c0016t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1312-1532A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591059 | ||||||
| chr3:129591102
|
G | A | 6 | a0001c0011t0001g0015a0001c0056t0001g0259a0003c0018t0005g0051others(3): Show | 10 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-1575C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591102 | ||||||
| chr3:129591222
|
C | T | 1 | a0002c0006t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312-1695G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591222 | ||||||
| chr3:129591241
|
G | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0101 | 2 | HG01993.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1312-1714C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591241 | ||||||
| chr3:129591348
|
C | T | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-1821G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591348 | ||||||
| chr3:129591350
|
C | T | 3 | a0002c0003t0003g0046a0002c0003t0003g0211a0002c0003t0003g0233 | 4 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-1823G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591350 | ||||||
| chr3:129591353
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01106.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1312-1826C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591353 | ||||||
| chr3:129591431
|
G | C | 2 | a0001c0001t0008g0036a0001c0001t0008g0173 | 3 | HG00639.hp1 HG02735.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1312-1904C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591431 | ||||||
| chr3:129591437
|
A | G | 3 | a0004c0004t0001g0056a0004c0004t0001g0297a0004c0004t0001g0298 | 4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-1910T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591437 | ||||||
| chr3:129591524
|
G | A | 4 | a0004c0004t0001g0241a0004c0004t0001g0252a0004c0004t0001g0253others(1): Show | 4 | HG00408.hp2 HG03927.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-1997C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591524 | ||||||
| chr3:129591562
|
A | G | 28 | a0003c0010t0001g0050a0004c0004t0001g0019a0004c0004t0001g0049others(25): Show | 32 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-2035T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591562 | ||||||
| chr3:129591799
|
C | T | 1 | a0006c0041t0001g0261 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1312-2272G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591799 | ||||||
| chr3:129591856
|
C | G | 1 | a0003c0008t0004g0294 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1312-2329G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591856 | ||||||
| chr3:129592057
|
C | A | 1 | a0004c0004t0001g0253 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1312-2530G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592057 | ||||||
| chr3:129592068
|
C | T | 2 | a0003c0008t0004g0293a0003c0008t0004g0294 | 2 | HG01168.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1312-2541G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592068 | ||||||
| chr3:129592109
|
C | G | 3 | a0002c0003t0003g0046a0002c0006t0001g0269a0031c0036t0001g0238 | 4 | HG00621.hp1 HG02132.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-2582G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592109 | ||||||
| chr3:129592375
|
A | T | 1 | a0002c0005t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1312-2848T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592375 | ||||||
| chr3:129592380
|
T | G | 28 | a0003c0010t0001g0050a0004c0004t0001g0019a0004c0004t0001g0049others(25): Show | 32 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-2853A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592380 | ||||||
| chr3:129592569
|
G | A | 2 | a0014c0025t0001g0154a0014c0025t0001g0255 | 2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1312-3042C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592569 | ||||||
| chr3:129592651
|
T | C | 1 | a0001c0002t0012g0095 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1312-3124A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592651 | ||||||
| chr3:129592686
|
T | C | 62 | a0001c0001t0001g0264a0001c0011t0001g0015a0001c0011t0001g0212others(59): Show | 89 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1312-3159A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592686 | ||||||
| chr3:129592721
|
A | G | 2 | a0002c0015t0006g0117a0002c0015t0006g0146 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1312-3194T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592721 | ||||||
| chr3:129592725
|
T | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1312-3198A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592725 | ||||||
| chr3:129592773
|
G | A | 60 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(57): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1312-3246C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592773 | ||||||
| chr3:129592839
|
C | T | 1 | a0001c0002t0002g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1312-3312G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592839 | ||||||
| chr3:129592959
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0174a0002c0005t0001g0188 | 4 | NA18980.hp1 NA18986.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-3432C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592959 | ||||||
| chr3:129592977
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0145 | 5 | HG00099.hp1 HG01123.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-3450G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592977 | ||||||
| chr3:129593034
|
G | C | 2 | a0002c0006t0001g0007a0002c0006t0001g0289 | 6 | HG01255.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-3507C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593034 | ||||||
| chr3:129593135
|
C | T | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-3608G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593135 | ||||||
| chr3:129593161
|
C | T | 6 | a0001c0011t0001g0015a0001c0056t0001g0259a0003c0018t0005g0051others(3): Show | 10 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-3634G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593161 | ||||||
| chr3:129593169
|
T | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-3642A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593169 | ||||||
| chr3:129593264
|
C | T | 1 | a0003c0014t0004g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1312-3737G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593264 | ||||||
| chr3:129593433
|
G | A | 1 | a0026c0062t0002g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1312-3906C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593433 | ||||||
| chr3:129593495
|
G | A | 1 | a0003c0007t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1312-3968C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593495 | ||||||
| chr3:129593588
|
C | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1312-4061G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593588 | ||||||
| chr3:129593845
|
C | T | 1 | a0032c0034t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1312-4318G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593845 | ||||||
| chr3:129593858
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0256 | 2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1312-4331C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593858 | ||||||
| chr3:129594059
|
C | T | 1 | a0004c0004t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1312-4532G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594059 | ||||||
| chr3:129594138
|
G | A | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-4611C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594138 | ||||||
| chr3:129594146
|
A | G | 154 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0008others(151): Show | 202 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.1312-4619T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594146 | ||||||
| chr3:129594384
|
G | A | 1 | a0002c0050t0009g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1312-4857C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594384 | ||||||
| chr3:129594387
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312-4860G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594387 | ||||||
| chr3:129594478
|
T | A | 1 | a0002c0003t0003g0225 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1312-4951A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594478 | ||||||
| chr3:129594530
|
T | C | 1 | a0001c0002t0002g0073 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1312-5003A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594530 | ||||||
| chr3:129594564
|
C | T | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5037G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594564 | ||||||
| chr3:129594566
|
T | C | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5039A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594566 | ||||||
| chr3:129594567
|
C | T | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5040G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594567 | ||||||
| chr3:129594586
|
C | A | 1 | a0015c0027t0001g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1312-5059G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594586 | ||||||
| chr3:129594595
|
C | A | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1312-5068G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594595 | ||||||
| chr3:129594646
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-5119T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594646 | ||||||
| chr3:129594661
|
A | G | 1 | a0012c0024t0004g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-5134T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594661 | ||||||
| chr3:129594662
|
G | A | 1 | a0012c0024t0004g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-5135C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594662 | ||||||
| chr3:129594678
|
G | A | 1 | a0004c0019t0004g0249 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1312-5151C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594678 | ||||||
| chr3:129594707
|
A | G | 1 | a0003c0008t0004g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1312-5180T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594707 | ||||||
| chr3:129594754
|
C | T | 1 | a0001c0002t0002g0072 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-5227G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594754 | ||||||
| chr3:129594788
|
C | T | 2 | a0002c0006t0001g0010a0002c0006t0001g0123 | 5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-5261G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594788 | ||||||
| chr3:129594806
|
C | G | 1 | a0003c0014t0004g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1312-5279G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594806 | ||||||
| chr3:129594869
|
T | TA | 8 | a0001c0001t0001g0176a0001c0001t0001g0191a0001c0002t0002g0071others(5): Show | 8 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-5343dupT | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | ||||||
| chr3:129594869
|
T | TAA | 144 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0008others(141): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1312-5344_1312-534 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | ||||||
| chr3:129594869
|
T | TAAA | 6 | a0001c0002t0002g0073a0001c0002t0002g0076a0002c0003t0003g0207others(3): Show | 6 | HG03239.hp2 NA18954.hp2 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-5345_1312-534 others(7): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | ||||||
| chr3:129594991
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0142a0002c0017t0007g0143 | 4 | HG00140.hp1 HG01258.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-5464T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594991 | ||||||
| chr3:129595102
|
G | GATGGGCT others(1): Show |
17 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(14): Show | 24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5576_1312-557 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595102 | ||||||
| chr3:129595104
|
C | A | 17 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(14): Show | 24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5577G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595104 | ||||||
| chr3:129595107
|
T | TGG | 17 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(14): Show | 24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5581_1312-558 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595107 | ||||||
| chr3:129595189
|
T | G | 3 | a0007c0021t0002g0023a0007c0021t0004g0069a0030c0060t0002g0070 | 4 | HG01243.hp1 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-5662A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595189 | ||||||
| chr3:129595242
|
T | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-5715A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595242 | ||||||
| chr3:129595345
|
C | T | 1 | a0002c0005t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1312-5818G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595345 | ||||||
| chr3:129595416
|
T | A | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1312-5889A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595416 | ||||||
| chr3:129595416
|
T | G | 151 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0008others(148): Show | 199 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1312-5889A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595416 | ||||||
| chr3:129595427
|
G | A | 6 | a0003c0008t0004g0038a0003c0008t0004g0039a0003c0008t0004g0177others(3): Show | 8 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-5900C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595427 | ||||||
| chr3:129595546
|
G | C | 1 | a0002c0012t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1312-6019C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595546 | ||||||
| chr3:129595596
|
G | A | 61 | a0001c0001t0001g0264a0001c0011t0001g0015a0001c0011t0001g0212others(58): Show | 88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1312-6069C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595596 | ||||||
| chr3:129595654
|
A | G | 1 | a0003c0007t0001g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1312-6127T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595654 | ||||||
| chr3:129595916
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-6389G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595916 | ||||||
| chr3:129595919
|
A | ACG | 2 | a0007c0021t0002g0023a0007c0021t0004g0069 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1312-6394_1312-639 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595919 | ||||||
| chr3:129595921
|
G | GCA | 18 | a0002c0003t0003g0210a0003c0010t0001g0050a0004c0004t0001g0049others(15): Show | 20 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-6396_1312-639 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACA | 22 | a0001c0001t0001g0142a0001c0001t0001g0264a0001c0011t0001g0015others(19): Show | 31 | HG00408.hp2 HG00673.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1312-6398_1312-639 others(8): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACA | 33 | a0001c0011t0001g0212a0001c0011t0001g0215a0001c0013t0003g0014others(30): Show | 49 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1312-6400_1312-639 others(10): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(1): Show |
63 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0029others(60): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1312-6402_1312-639 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(3): Show |
73 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(70): Show | 101 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1312-6404_1312-639 others(14): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(5): Show |
18 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0065others(15): Show | 20 | HG00597.hp1 HG01255.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-6406_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(7): Show |
1 | a0001c0001t0001g0192 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1312-6408_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(9): Show |
1 | a0001c0047t0002g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-6410_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACACAC others(11): Show |
2 | a0001c0020t0001g0132a0002c0050t0009g0120 | 2 | HG00735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1312-6412_1312-639 others(22): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACGCAC others(5): Show |
1 | a0002c0070t0011g0305 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCACGCAC others(7): Show |
1 | a0001c0069t0011g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCCACACA others(4): Show |
1 | a0001c0001t0001g0180 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(15): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACA | 3 | a0001c0002t0002g0075a0001c0002t0002g0076a0027c0063t0002g0074 | 3 | HG02523.hp2 NA19055.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(10): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(1): Show |
2 | a0001c0002t0002g0008a0001c0002t0002g0112 | 5 | HG02080.hp2 HG03669.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(3): Show |
5 | a0001c0002t0002g0062a0001c0002t0002g0078a0001c0002t0002g0110others(2): Show | 5 | HG00438.hp1 NA18944.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(14): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(5): Show |
4 | a0001c0002t0002g0079a0001c0002t0002g0081a0001c0002t0002g0082others(1): Show | 4 | HG00423.hp1 HG00642.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(7): Show |
18 | a0001c0002t0002g0005a0001c0002t0002g0024a0001c0002t0002g0068others(15): Show | 24 | HG00597.hp2 HG00609.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(9): Show |
11 | a0001c0002t0002g0016a0001c0002t0002g0073a0001c0002t0002g0097others(8): Show | 17 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(11): Show |
10 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0104others(7): Show | 11 | HG00140.hp2 HG01069.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(22): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(13): Show |
1 | a0001c0002t0002g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(24): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCACAC others(15): Show |
2 | a0001c0002t0002g0111a0001c0002t0002g0113 | 2 | NA18952.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(26): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCGCAC others(7): Show |
1 | a0001c0002t0002g0072 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCGCAC others(9): Show |
1 | a0001c0002t0002g0083 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCGCAC others(17): Show |
1 | a0001c0002t0002g0108 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(28): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595921
|
G | GCGCGCAC others(19): Show |
1 | a0001c0002t0002g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(30): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | ||||||
| chr3:129595923
|
A | G | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6396T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595923 | ||||||
| chr3:129595946
|
C | CACACACA others(7): Show |
1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6420_1312-641 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595946 | ||||||
| chr3:129595949
|
T | A | 150 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0008others(147): Show | 198 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.1312-6422A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595949 | ||||||
| chr3:129596024
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-6497T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596024 | ||||||
| chr3:129596052
|
G | A | 12 | a0002c0005t0001g0287a0002c0006t0001g0007a0002c0006t0001g0269others(9): Show | 18 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1312-6525C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596052 | ||||||
| chr3:129596189
|
G | C | 3 | a0007c0021t0002g0023a0007c0021t0004g0069a0030c0060t0002g0070 | 4 | HG01243.hp1 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-6662C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596189 | ||||||
| chr3:129596236
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1312-6709C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596236 | ||||||
| chr3:129596262
|
C | G | 1 | a0004c0004t0001g0243 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1312-6735G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596262 | ||||||
| chr3:129596294
|
C | T | 1 | a0001c0002t0002g0073 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1312-6767G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596294 | ||||||
| chr3:129596301
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1312-6774C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596301 | ||||||
| chr3:129596408
|
C | G | 1 | a0002c0015t0006g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1312-6881G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596408 | ||||||
| chr3:129596445
|
C | A | 1 | a0002c0005t0001g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1312-6918G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596445 | ||||||
| chr3:129596453
|
C | T | 17 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(14): Show | 24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-6926G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596453 | ||||||
| chr3:129596526
|
T | A | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6999A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596526 | ||||||
| chr3:129596624
|
C | G | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-7097G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596624 | ||||||
| chr3:129596644
|
G | A | 64 | a0001c0001t0001g0189a0001c0002t0002g0005a0001c0002t0002g0008others(61): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1312-7117C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596644 | ||||||
| chr3:129596735
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0141 | 3 | NA18981.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1312-7208G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596735 | ||||||
| chr3:129596736
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-7209T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596736 | ||||||
| chr3:129596738
|
C | G | 1 | a0012c0024t0004g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-7211G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596738 | ||||||
| chr3:129596843
|
A | T | 1 | a0002c0003t0003g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1312-7316T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596843 | ||||||
| chr3:129596886
|
C | T | 1 | a0001c0002t0002g0072 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-7359G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596886 | ||||||
| chr3:129596887
|
G | A | 1 | a0019c0055t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1312-7360C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596887 | ||||||
| chr3:129596926
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(147): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1312-7399C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596926 | ||||||
| chr3:129596988
|
C | A | 124 | a0001c0001t0001g0264a0001c0002t0002g0005a0001c0002t0002g0008others(121): Show | 168 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1312-7461G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596988 | ||||||
| chr3:129597176
|
G | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1312-7649C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597176 | ||||||
| chr3:129597212
|
T | C | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-7685A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597212 | ||||||
| chr3:129597417
|
G | T | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-7890C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597417 | ||||||
| chr3:129597424
|
G | C | 11 | a0002c0005t0001g0287a0002c0006t0001g0007a0002c0006t0001g0285others(8): Show | 17 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1312-7897C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597424 | ||||||
| chr3:129597483
|
G | GC | 17 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0190others(14): Show | 17 | HG00423.hp2 HG01515.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1311+7845dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597483 | ||||||
| chr3:129597492
|
C | CCCA | 23 | a0003c0010t0001g0050a0004c0004t0001g0019a0004c0004t0001g0049others(20): Show | 27 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1311+7836_1311+783 others(7): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597492 | ||||||
| chr3:129597559
|
G | A | 1 | a0001c0069t0011g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1311+7770C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597559 | ||||||
| chr3:129597585
|
C | G | 2 | a0001c0001t0001g0203a0002c0005t0001g0139 | 2 | HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1311+7744G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597585 | ||||||
| chr3:129597636
|
G | A | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+7693C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597636 | ||||||
| chr3:129597701
|
G | T | 1 | a0001c0002t0002g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1311+7628C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597701 | ||||||
| chr3:129597751
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(299): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1311+7578C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597751 | ||||||
| chr3:129597801
|
G | C | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1311+7528C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597801 | ||||||
| chr3:129597824
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+7505G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597824 | ||||||
| chr3:129597930
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1311+7399A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597930 | ||||||
| chr3:129598134
|
G | A | 1 | a0002c0003t0003g0237 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1311+7195C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598134 | ||||||
| chr3:129598284
|
C | T | 2 | a0002c0006t0001g0010a0002c0006t0001g0123 | 5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+7045G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598284 | ||||||
| chr3:129598402
|
T | C | 60 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(57): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1311+6927A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598402 | ||||||
| chr3:129598461
|
G | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1311+6868C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598461 | ||||||
| chr3:129598472
|
C | A | 1 | a0017c0058t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+6857G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598472 | ||||||
| chr3:129598504
|
T | C | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+6825A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598504 | ||||||
| chr3:129598509
|
G | A | 61 | a0001c0001t0001g0264a0001c0011t0001g0015a0001c0011t0001g0212others(58): Show | 88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1311+6820C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598509 | ||||||
| chr3:129598644
|
G | T | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1311+6685C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598644 | ||||||
| chr3:129598658
|
C | T | 1 | a0006c0023t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1311+6671G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598658 | ||||||
| chr3:129598659
|
G | A | 1 | a0002c0006t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1311+6670C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598659 | ||||||
| chr3:129598742
|
C | T | 61 | a0001c0001t0001g0264a0001c0011t0001g0015a0001c0011t0001g0212others(58): Show | 88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1311+6587G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598742 | ||||||
| chr3:129598838
|
A | G | 1 | a0001c0002t0002g0068 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1311+6491T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598838 | ||||||
| chr3:129598902
|
G | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1311+6427C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598902 | ||||||
| chr3:129598931
|
T | C | 1 | a0001c0002t0002g0112 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1311+6398A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598931 | ||||||
| chr3:129598936
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1311+6393T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598936 | ||||||
| chr3:129599213
|
C | T | 1 | a0002c0003t0003g0043 | 2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1311+6116G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599213 | ||||||
| chr3:129599260
|
C | T | 1 | a0001c0002t0002g0067 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1311+6069G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599260 | ||||||
| chr3:129599435
|
C | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(276): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1311+5894G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599435 | ||||||
| chr3:129599451
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02280.hp1 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+5878G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599451 | ||||||
| chr3:129599751
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0124others(10): Show | 17 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1311+5578T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599751 | ||||||
| chr3:129599880
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+5449G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599880 | ||||||
| chr3:129600020
|
A | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+5309T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600020 | ||||||
| chr3:129600026
|
G | A | 1 | a0004c0004t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1311+5303C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600026 | ||||||
| chr3:129600039
|
C | T | 1 | a0001c0002t0002g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1311+5290G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600039 | ||||||
| chr3:129600206
|
G | A | 63 | a0001c0002t0002g0005a0001c0002t0002g0008a0001c0002t0002g0016others(60): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1311+5123C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600206 | ||||||
| chr3:129600439
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1311+4890C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600439 | ||||||
| chr3:129600655
|
G | A | 1 | a0008c0022t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+4674C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600655 | ||||||
| chr3:129600719
|
C | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1311+4610G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600719 | ||||||
| chr3:129600741
|
C | G | 1 | a0017c0058t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+4588G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600741 | ||||||
| chr3:129601293
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1311+4036C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601293 | ||||||
| chr3:129601325
|
T | C | 1 | a0019c0055t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1311+4004A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601325 | ||||||
| chr3:129601330
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0199 | 4 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+3999C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601330 | ||||||
| chr3:129601443
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1311+3886C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601443 | ||||||
| chr3:129601458
|
G | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(213): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1311+3871C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601458 | ||||||
| chr3:129601465
|
C | T | 3 | a0002c0005t0001g0028a0002c0005t0001g0126a0002c0005t0001g0127 | 4 | HG01069.hp1 HG01071.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+3864G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601465 | ||||||
| chr3:129601655
|
A | G | 1 | a0003c0008t0004g0293 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1311+3674T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601655 | ||||||
| chr3:129601685
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1311+3644T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601685 | ||||||
| chr3:129601687
|
A | G | 55 | a0001c0001t0001g0264a0001c0011t0001g0212a0001c0011t0001g0215others(52): Show | 78 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1311+3642T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601687 | ||||||
| chr3:129601914
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(235): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1311+3415G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601914 | ||||||
| chr3:129601957
|
C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1311+3372G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601957 | ||||||
| chr3:129602225
|
C | T | 2 | a0001c0069t0011g0306a0002c0070t0011g0305 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+3104G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602225 | ||||||
| chr3:129602272
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1311+3057G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602272 | ||||||
| chr3:129602477
|
C | T | 2 | a0002c0006t0001g0010a0002c0006t0001g0123 | 5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+2852G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602477 | ||||||
| chr3:129602478
|
G | A | 9 | a0001c0001t0001g0264a0003c0007t0001g0266a0003c0010t0001g0020others(6): Show | 11 | HG01099.hp1 HG01358.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+2851C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602478 | ||||||
| chr3:129602649
|
T | C | 1 | a0002c0012t0001g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1311+2680A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602649 | ||||||
| chr3:129602767
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(298): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1311+2562T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602767 | ||||||
| chr3:129602922
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1311+2407C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602922 | ||||||
| chr3:129602997
|
A | T | 3 | a0004c0004t0001g0056a0004c0004t0001g0297a0004c0004t0001g0298 | 4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+2332T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602997 | ||||||
| chr3:129603010
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(298): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1311+2319T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603010 | ||||||
| chr3:129603555
|
G | A | 2 | a0002c0005t0001g0055a0002c0005t0001g0291 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1311+1774C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603555 | ||||||
| chr3:129603679
|
G | A | 1 | a0003c0014t0004g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1311+1650C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603679 | ||||||
| chr3:129603768
|
C | T | 1 | a0008c0022t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+1561G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603768 | ||||||
| chr3:129603973
|
A | G | 62 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0002t0002g0005others(59): Show | 79 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1311+1356T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603973 | ||||||
| chr3:129603981
|
G | A | 176 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0256others(173): Show | 237 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.1311+1348C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603981 | ||||||
| chr3:129604176
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(304): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.1311+1153A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604176 | ||||||
| chr3:129604298
|
C | A | 3 | a0009c0032t0005g0268a0009c0033t0005g0267a0017c0058t0014g0270 | 3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1311+1031G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604298 | ||||||
| chr3:129604465
|
T | C | 1 | a0002c0006t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1311+864A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604465 | ||||||
| chr3:129604479
|
T | C | 1 | a0001c0001t0001g0021 | 3 | HG00323.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1311+850A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604479 | ||||||
| chr3:129605133
|
G | A | 1 | a0017c0058t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+196C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605133 | ||||||
| chr3:129605162
|
G | A | 28 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(25): Show | 41 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.1311+167C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605162 | ||||||
| chr3:129605173
|
T | C | 4 | a0001c0001t0001g0295a0003c0008t0004g0293a0003c0008t0004g0294others(1): Show | 4 | HG01167.hp2 HG01168.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+156A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605173 | ||||||
| chr3:129605265
|
G | GCCCGCC | 3 | a0004c0004t0001g0056a0004c0004t0001g0297a0004c0004t0001g0298 | 4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+58_1311+63dup others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605265 | ||||||
| chr3:129605265
|
GCCCGCC | G | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG00735.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+58_1311+63del others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605265 | ||||||
| chr3:129605284
|
C | CCCG | 61 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(58): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1311+42_1311+44dup others(3): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | ||||||
| chr3:129605284
|
C | CCCGCCGC others(8): Show |
1 | a0001c0002t0002g0062 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1311+30_1311+44dup others(15): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | ||||||
| chr3:129605284
|
CCCGCCGC others(5): Show |
C | 3 | a0002c0003t0003g0300a0002c0003t0003g0301a0002c0003t0003g0302 | 3 | HG03710.hp2 NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1311+33_1311+44del others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | ||||||
| chr3:129605285
|
C | A | 1 | a0004c0004t0001g0299 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1311+44G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605285 |