Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26003 |
|---|---|
| ensemblid | ENSG00000115806.13 |
| hgncid | 17500 |
| symbol | GORASP2 |
| name | golgi reassembly stacking protein 2 |
| refseq_nuc | NM_015530.5 |
| refseq_prot | NP_056345.3 |
| ensembl_nuc | ENST00000234160.5 |
| ensembl_prot | ENSP00000234160.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 170929253 |
| end | 170967130 |
| strand | + |
| ver | v1.2 |
| region | chr2:170929253-170967130 |
| region5000 | chr2:170924253-170972130 |
| regionname0 | GORASP2_chr2_170929253_170967130 |
| regionname5000 | GORASP2_chr2_170924253_170972130 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 301 | 85 | 55 | 107 | 16 | 36 | 76 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0002 | 0/0 | 452 | 68 | 0 | 9 | 53 | 0 | 6 | 39 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0003 | 0/0 | 452 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0004 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0005 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0006 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0007 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1359 | 253 | 45 | 51 | 107 | 15 | 34 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0002 | 0/0 | 1359 | 68 | 0 | 9 | 53 | 0 | 6 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0003 | 1/0 | 1359 | 46 | 38 | 4 | 0 | 1 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0004 | 0/0 | 1359 | 8 | 6 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0005 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0007 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0008 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0009 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1089 | 369 | 90 | 60 | 162 | 16 | 39 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0002 | 0/0 | 1089 | 6 | 0 | 4 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0003 | 0/0 | 1089 | 2 | 0 | 1 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0004 | 0/0 | 1089 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0005 | 0/0 | 1089 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0006 | 0/0 | 1089 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| t0007 | 0/0 | 1089 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 19 | 2 | 4 | 10 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0002 | 0/0 | 9 | 0 | 7 | 1 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0003 | 0/0 | 7 | 1 | 1 | 5 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0004 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0007 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1359 | 253 | 45 | 51 | 107 | 15 | 34 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0003 | 1/0 | 1359 | 46 | 38 | 4 | 0 | 1 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0009 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0002c0002 | 0/0 | 1359 | 68 | 0 | 9 | 53 | 0 | 6 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0003c0004 | 0/0 | 1359 | 8 | 6 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0004c0005 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0005c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0006c0007 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0007c0008 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2447 | 246 | 43 | 49 | 105 | 15 | 33 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0001t0003 | 0/0 | 2447 | 2 | 0 | 1 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0001t0004 | 0/0 | 2447 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0001t0005 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0001t0006 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0001t0007 | 0/0 | 2447 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0003t0001 | 1/0 | 2447 | 40 | 38 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0003t0002 | 0/0 | 2447 | 6 | 0 | 4 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0006t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0001c0009t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0002c0002t0001 | 0/0 | 2447 | 68 | 0 | 9 | 53 | 0 | 6 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0003c0004t0001 | 0/0 | 2447 | 8 | 6 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0004c0005t0001 | 0/0 | 2447 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0005c0010t0001 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0006c0007t0001 | 0/0 | 2447 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| a0007c0008t0001 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | copy fasta | chr2 | 170924253 | 170972130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 3 | 10 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 7 | 1 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0003 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0007 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0001c0009t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0003c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0004c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0004c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0005c0010t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0006c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| a0007c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | CHS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0073 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0232 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02015 | hp1 | a0005 | c0010 | t0001 | g0079 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | CDX | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0072 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0186 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0200 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0038 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0183 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03041 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0259 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0231 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | GWD | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0071 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | CHB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | YRI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18972 | hp1 | a0006 | c0007 | t0001 | g0158 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19009 | hp2 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19068 | hp1 | a0004 | c0005 | t0001 | g0003 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ASW | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20129 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ASW | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | GIH | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA21309 | hp1 | a0007 | c0008 | t0001 | g0049 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0046 | REF | REF | GORASP2_chr2_170924253_170972130 | GORASP2 | chr2 | 170924253 | 170972130 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170956451
|
G | T | 1 | a0005 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.715G>T | p.Val239Phe | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/10 | 803/2447 | 715/1359 | 239/452 | chr2 | 170956451 | ||
| chr2:170956461
|
C | T | 1 | a0004 | 2 | NA19009.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.725C>T | p.Pro242Leu | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/10 | 813/2447 | 725/1359 | 242/452 | chr2 | 170956461 | ||
| chr2:170966015
|
C | T | 1 | a0003 | 8 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(5): Show |
missense_variant | MODERATE | c.1244C>T | p.Thr415Met | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1332/2447 | 1244/1359 | 415/452 | chr2 | 170966015 | ||
| chr2:170966044
|
G | A | 1 | a0006 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1273G>A | p.Val425Ile | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1361/2447 | 1273/1359 | 425/452 | chr2 | 170966044 | ||
| chr2:170966062
|
G | A | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1291G>A | p.Asp431Asn | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1379/2447 | 1291/1359 | 431/452 | chr2 | 170966062 | ||
| chr2:170966066
|
C | T | 1 | a0002 | 68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
missense_variant | MODERATE | c.1295C>T | p.Ser432Phe | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1383/2447 | 1295/1359 | 432/452 | chr2 | 170966066 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170961679
|
G | A | 1 | a0001c0006 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.840G>A | p.Pro280Pro | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/10 | 928/2447 | 840/1359 | 280/452 | chr2 | 170961679 | ||
| chr2:170965849
|
C | T | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1078C>T | p.Leu360Leu | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1166/2447 | 1078/1359 | 360/452 | chr2 | 170965849 | ||
| chr2:170965956
|
C | T | 9 | a0001c0001a0001c0006a0001c0009others(6): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
synonymous_variant | LOW | c.1185C>T | p.Ser395Ser | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 1273/2447 | 1185/1359 | 395/452 | chr2 | 170965956 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170929265
|
G | C | 1 | a0001c0001t0005 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/10 | 76 | chr2 | 170929265 | |||||
| chr2:170966335
|
C | T | 1 | a0001c0003t0002 | 6 | HG01069.hp1 HG01081.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 205 | chr2 | 170966335 | |||||
| chr2:170966364
|
T | C | 1 | a0001c0001t0006 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 234 | chr2 | 170966364 | |||||
| chr2:170966420
|
G | A | 1 | a0001c0001t0007 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 290 | chr2 | 170966420 | |||||
| chr2:170966558
|
C | G | 1 | a0001c0001t0004 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*428C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 428 | chr2 | 170966558 | |||||
| chr2:170966638
|
T | C | 1 | a0001c0001t0003 | 2 | HG00733.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*508T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 10/10 | 508 | chr2 | 170966638 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170929509
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.63+106C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929509 | ||||||
| chr2:170929553
|
G | A | 2 | a0001c0003t0001g0020a0003c0004t0001g0038 | 3 | HG02970.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+150G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929553 | ||||||
| chr2:170929578
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(27): Show | 41 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.63+175C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929578 | ||||||
| chr2:170929659
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.63+256A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929659 | ||||||
| chr2:170929719
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 7 | HG00323.hp1 HG00738.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+316C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929719 | ||||||
| chr2:170929729
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+326C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929729 | ||||||
| chr2:170929737
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.63+334T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929737 | ||||||
| chr2:170929772
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(6): Show | 10 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+369G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929772 | ||||||
| chr2:170929784
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.63+381G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929784 | ||||||
| chr2:170929876
|
C | T | 4 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0252others(1): Show | 4 | NA18952.hp1 NA18962.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+473C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929876 | ||||||
| chr2:170929928
|
C | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+525C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929928 | ||||||
| chr2:170929964
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 7 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+561G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929964 | ||||||
| chr2:170929969
|
G | A | 4 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+566G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170929969 | ||||||
| chr2:170930013
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+610C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930013 | ||||||
| chr2:170930053
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+650C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930053 | ||||||
| chr2:170930083
|
TTA | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+683_63+684delTA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930083 | |||||
| chr2:170930351
|
A | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+948A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930351 | ||||||
| chr2:170930368
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG01346.hp1 HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.63+965C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930368 | ||||||
| chr2:170930377
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+974G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930377 | ||||||
| chr2:170930651
|
A | AT | 69 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0062others(66): Show | 89 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.63+1258dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930651 | |||||
| chr2:170930740
|
A | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(30): Show | 44 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+1337A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930740 | ||||||
| chr2:170930973
|
CA | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0019others(111): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.63+1587delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170930973 | |||||
| chr2:170930988
|
A | AC | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.63+1585_63+1586ins others(1): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930988 | ||||||
| chr2:170930988
|
A | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0019others(110): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.63+1585A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170930988 | ||||||
| chr2:170931097
|
G | GA | 8 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+1697dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170931097 | |||||
| chr2:170931213
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.63+1810C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931213 | ||||||
| chr2:170931514
|
T | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+2111T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931514 | ||||||
| chr2:170931949
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.63+2546C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170931949 | ||||||
| chr2:170932001
|
G | A | 1 | a0002c0002t0001g0194 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.63+2598G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932001 | ||||||
| chr2:170932018
|
G | A | 1 | a0005c0010t0001g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+2615G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932018 | ||||||
| chr2:170932136
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.63+2733A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932136 | ||||||
| chr2:170932203
|
G | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.63+2800G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932203 | ||||||
| chr2:170932296
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.63+2893A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932296 | ||||||
| chr2:170932403
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.63+3000T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932403 | ||||||
| chr2:170932693
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+3290C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170932693 | ||||||
| chr2:170933192
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.63+3789T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933192 | ||||||
| chr2:170933214
|
C | T | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+3811C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933214 | ||||||
| chr2:170933587
|
A | C | 1 | a0002c0002t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+4184A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933587 | ||||||
| chr2:170933593
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.63+4190C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933593 | ||||||
| chr2:170933657
|
T | C | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.63+4254T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933657 | ||||||
| chr2:170933697
|
G | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02602.hp2 HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.63+4294G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933697 | ||||||
| chr2:170933707
|
TAAAAG | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+4306_63+4310del others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170933707 | |||||
| chr2:170933843
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.63+4440A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933843 | ||||||
| chr2:170933877
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.63+4474A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933877 | ||||||
| chr2:170933986
|
T | TA | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+4584dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170933986 | |||||
| chr2:170933987
|
A | G | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.63+4584A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170933987 | ||||||
| chr2:170934158
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0081 | 3 | NA18975.hp2 NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.63+4755T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934158 | ||||||
| chr2:170934197
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+4794C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934197 | ||||||
| chr2:170934244
|
CCT | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+4842_63+4843del others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934244 | ||||||
| chr2:170934253
|
T | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+4850T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934253 | ||||||
| chr2:170934256
|
T | G | 20 | a0001c0001t0001g0082a0001c0001t0001g0246a0001c0001t0001g0247others(17): Show | 21 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+4853T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934256 | ||||||
| chr2:170934258
|
TG | T | 3 | a0001c0001t0001g0098a0002c0002t0001g0199a0003c0004t0001g0200 | 3 | HG02818.hp1 HG02965.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.63+4856delG | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934258 | ||||||
| chr2:170934259
|
G | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 260 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.63+4856G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934259 | ||||||
| chr2:170934262
|
G | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0002c0002t0001g0239 | 3 | HG02165.hp1 NA18947.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.63+4859G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934262 | ||||||
| chr2:170934305
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.63+4902C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934305 | ||||||
| chr2:170934556
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.63+5153C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934556 | ||||||
| chr2:170934801
|
A | G | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+5398A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934801 | ||||||
| chr2:170934899
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.63+5496A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170934899 | ||||||
| chr2:170935077
|
T | C | 1 | a0002c0002t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+5674T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935077 | ||||||
| chr2:170935526
|
A | G | 7 | a0002c0002t0001g0198a0002c0002t0001g0233a0002c0002t0001g0234others(4): Show | 7 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+6123A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935526 | ||||||
| chr2:170935558
|
C | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6155C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935558 | ||||||
| chr2:170935572
|
C | CT | 8 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 9 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6187dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170935572 | |||||
| chr2:170935585
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63+6182T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935585 | ||||||
| chr2:170935588
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.63+6185T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935588 | ||||||
| chr2:170935588
|
T | TC | 4 | a0003c0004t0001g0011a0003c0004t0001g0200a0003c0004t0001g0231others(1): Show | 7 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6185_63+6186ins others(1): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935588 | ||||||
| chr2:170935781
|
G | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6378G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935781 | ||||||
| chr2:170935815
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+6412A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935815 | ||||||
| chr2:170935919
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.63+6516C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935919 | ||||||
| chr2:170935922
|
C | T | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0096others(17): Show | 22 | HG00099.hp1 HG00639.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+6519C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935922 | ||||||
| chr2:170935953
|
G | T | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+6550G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170935953 | ||||||
| chr2:170936019
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.63+6616C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936019 | ||||||
| chr2:170936082
|
C | G | 1 | a0001c0003t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.63+6679C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936082 | ||||||
| chr2:170936224
|
C | CT | 36 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0027others(33): Show | 51 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.63+6841dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | |||||
| chr2:170936224
|
C | CTT | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.63+6840_63+6841dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | |||||
| chr2:170936224
|
C | CTTT | 8 | a0001c0001t0001g0025a0001c0001t0001g0076a0001c0001t0001g0170others(5): Show | 9 | HG02486.hp1 HG02647.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6839_63+6841dup others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170936224 | |||||
| chr2:170936406
|
A | G | 12 | a0002c0002t0001g0009a0002c0002t0001g0036a0002c0002t0001g0188others(9): Show | 17 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+7003A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936406 | ||||||
| chr2:170936420
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0080 | 3 | HG00280.hp1 HG03710.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.63+7017A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936420 | ||||||
| chr2:170936464
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.63+7061C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936464 | ||||||
| chr2:170936629
|
A | G | 4 | a0001c0003t0002g0071a0001c0003t0002g0072a0001c0003t0002g0073others(1): Show | 4 | HG01081.hp2 HG02735.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+7226A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936629 | ||||||
| chr2:170936758
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0093others(2): Show | 5 | HG00140.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7355C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936758 | ||||||
| chr2:170936833
|
G | A | 1 | a0001c0003t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+7430G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936833 | ||||||
| chr2:170936847
|
C | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+7444C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936847 | ||||||
| chr2:170936876
|
C | T | 4 | a0003c0004t0001g0011a0003c0004t0001g0200a0003c0004t0001g0231others(1): Show | 7 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7473C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936876 | ||||||
| chr2:170936914
|
A | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0063others(12): Show | 20 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+7511A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170936914 | ||||||
| chr2:170937058
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+7655A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937058 | ||||||
| chr2:170937077
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.63+7674G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937077 | ||||||
| chr2:170937187
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.63+7784G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937187 | ||||||
| chr2:170937786
|
C | T | 1 | a0002c0002t0001g0223 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+8383C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937786 | ||||||
| chr2:170937797
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 9 | HG00140.hp1 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8394A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937797 | ||||||
| chr2:170937869
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.63+8466T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937869 | ||||||
| chr2:170937998
|
C | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8595C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170937998 | ||||||
| chr2:170938024
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+8621C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938024 | ||||||
| chr2:170938051
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0245 | 2 | HG01081.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.63+8648C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938051 | ||||||
| chr2:170938118
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.63+8715G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938118 | ||||||
| chr2:170938121
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+8718A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938121 | ||||||
| chr2:170938172
|
A | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.63+8769A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938172 | ||||||
| chr2:170938509
|
C | T | 2 | a0002c0002t0001g0221a0002c0002t0001g0222 | 2 | NA18985.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.63+9106C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938509 | ||||||
| chr2:170938533
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.63+9130A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938533 | ||||||
| chr2:170938650
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+9247C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938650 | ||||||
| chr2:170938650
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.63+9247C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170938650 | ||||||
| chr2:170939001
|
G | GA | 4 | a0001c0001t0001g0096a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00099.hp1 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9342dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170939001 | |||||
| chr2:170939110
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-9240A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939110 | ||||||
| chr2:170939158
|
G | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9192G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939158 | ||||||
| chr2:170939202
|
T | C | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-9148T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939202 | ||||||
| chr2:170939331
|
G | A | 2 | a0001c0003t0001g0183a0001c0003t0001g0184 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-9019G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939331 | ||||||
| chr2:170939429
|
CA | C | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(52): Show | 69 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-8920delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939429 | ||||||
| chr2:170939506
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | NA18942.hp1 NA18978.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.64-8844C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939506 | ||||||
| chr2:170939591
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-8759T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939591 | ||||||
| chr2:170939745
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.64-8605A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939745 | ||||||
| chr2:170939917
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-8433A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170939917 | ||||||
| chr2:170940006
|
TAGA | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-8340_64-8338del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170940006 | |||||
| chr2:170940013
|
G | A | 1 | a0001c0003t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-8337G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940013 | ||||||
| chr2:170940037
|
A | G | 2 | a0001c0003t0001g0183a0001c0003t0001g0184 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-8313A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940037 | ||||||
| chr2:170940087
|
A | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8263A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940087 | ||||||
| chr2:170940221
|
A | G | 2 | a0002c0002t0001g0189a0002c0002t0001g0229 | 2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.64-8129A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940221 | ||||||
| chr2:170940259
|
C | G | 1 | a0001c0003t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-8091C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940259 | ||||||
| chr2:170940369
|
A | G | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-7981A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940369 | ||||||
| chr2:170940553
|
TAAAAG | T | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-7786_64-7782del others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170940553 | |||||
| chr2:170940609
|
A | C | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-7741A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940609 | ||||||
| chr2:170940679
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-7671G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940679 | ||||||
| chr2:170940724
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-7626A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940724 | ||||||
| chr2:170940881
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.64-7469T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170940881 | ||||||
| chr2:170941339
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64-7011G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941339 | ||||||
| chr2:170941394
|
A | G | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-6956A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941394 | ||||||
| chr2:170941574
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-6776A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941574 | ||||||
| chr2:170941619
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-6731T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941619 | ||||||
| chr2:170941868
|
T | C | 1 | a0001c0003t0001g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64-6482T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941868 | ||||||
| chr2:170941873
|
A | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0063others(10): Show | 18 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-6477A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170941873 | ||||||
| chr2:170942069
|
G | A | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-6281G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942069 | ||||||
| chr2:170942084
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-6266T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942084 | ||||||
| chr2:170942267
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.64-6083A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942267 | ||||||
| chr2:170942304
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64-6046A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942304 | ||||||
| chr2:170942431
|
A | G | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-5919A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942431 | ||||||
| chr2:170942447
|
C | T | 1 | a0001c0003t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-5903C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942447 | ||||||
| chr2:170942450
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-5900A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942450 | ||||||
| chr2:170942456
|
C | T | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-5894C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942456 | ||||||
| chr2:170942504
|
T | G | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-5846T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942504 | ||||||
| chr2:170942547
|
G | A | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-5803G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942547 | ||||||
| chr2:170942876
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-5474C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942876 | ||||||
| chr2:170942914
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-5436G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170942914 | ||||||
| chr2:170943181
|
GTTTTACC others(7): Show |
G | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-5163_64-5150del others(14): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170943181 | |||||
| chr2:170943205
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-5145T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943205 | ||||||
| chr2:170943401
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18968.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.64-4949G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943401 | ||||||
| chr2:170943418
|
T | G | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-4932T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943418 | ||||||
| chr2:170943632
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.64-4718A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943632 | ||||||
| chr2:170943655
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-4695A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943655 | ||||||
| chr2:170943771
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64-4579C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943771 | ||||||
| chr2:170943772
|
G | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-4578G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943772 | ||||||
| chr2:170943785
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-4565G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943785 | ||||||
| chr2:170943792
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-4558C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943792 | ||||||
| chr2:170943873
|
A | G | 3 | a0003c0004t0001g0011a0003c0004t0001g0200a0003c0004t0001g0232 | 6 | HG00733.hp1 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4477A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943873 | ||||||
| chr2:170943965
|
C | T | 1 | a0002c0002t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64-4385C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170943965 | ||||||
| chr2:170944043
|
A | C | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-4307A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944043 | ||||||
| chr2:170944176
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.64-4174A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944176 | ||||||
| chr2:170944273
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-4077A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944273 | ||||||
| chr2:170944286
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64-4064T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944286 | ||||||
| chr2:170944311
|
G | C | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-4039G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944311 | ||||||
| chr2:170944412
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64-3938A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944412 | ||||||
| chr2:170944437
|
G | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-3913G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944437 | ||||||
| chr2:170944564
|
A | C | 1 | a0001c0003t0001g0023 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.64-3786A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944564 | ||||||
| chr2:170944710
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 7 | HG02071.hp2 HG02135.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3640G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944710 | ||||||
| chr2:170944902
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.64-3448G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170944902 | ||||||
| chr2:170945212
|
G | A | 1 | a0002c0002t0001g0239 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-3138G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945212 | ||||||
| chr2:170945237
|
G | A | 1 | a0003c0004t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-3113G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945237 | ||||||
| chr2:170945258
|
C | T | 1 | a0002c0002t0001g0194 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.64-3092C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945258 | ||||||
| chr2:170945359
|
C | CGT | 2 | a0001c0001t0001g0024a0001c0001t0001g0058 | 3 | HG02886.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.64-2987_64-2986dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945359 | |||||
| chr2:170945501
|
C | CA | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.64-2835dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945501 | |||||
| chr2:170945501
|
C | CAA | 16 | a0001c0001t0001g0029a0001c0001t0001g0080a0001c0001t0001g0089others(13): Show | 17 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-2836_64-2835dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170945501 | |||||
| chr2:170945515
|
AGAAG | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2834_64-2831del others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945515 | ||||||
| chr2:170945516
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.64-2834G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945516 | ||||||
| chr2:170945649
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.64-2701G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945649 | ||||||
| chr2:170945688
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-2662T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945688 | ||||||
| chr2:170945726
|
A | G | 6 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | HG03130.hp1 HG04199.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-2624A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945726 | ||||||
| chr2:170945823
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.64-2527T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945823 | ||||||
| chr2:170945964
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0279 | 2 | HG02559.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.64-2386A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170945964 | ||||||
| chr2:170946010
|
T | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0268a0002c0002t0001g0224 | 3 | HG02523.hp2 HG02886.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.64-2340T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946010 | ||||||
| chr2:170946318
|
C | T | 54 | a0002c0002t0001g0005a0002c0002t0001g0009a0002c0002t0001g0010others(51): Show | 68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.64-2032C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946318 | ||||||
| chr2:170946424
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.64-1926A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946424 | ||||||
| chr2:170946620
|
G | C | 1 | a0002c0002t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-1730G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946620 | ||||||
| chr2:170946768
|
C | CA | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.64-1562dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170946768 | |||||
| chr2:170946768
|
C | CAA | 35 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0074others(32): Show | 40 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1563_64-1562dup others(2): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170946768 | |||||
| chr2:170946881
|
A | C | 1 | a0001c0003t0001g0148 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64-1469A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170946881 | ||||||
| chr2:170947010
|
G | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | HG03130.hp1 HG04199.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-1340G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947010 | ||||||
| chr2:170947081
|
T | C | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.64-1269T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947081 | ||||||
| chr2:170947129
|
T | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(26): Show | 40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1221T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947129 | ||||||
| chr2:170947281
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64-1069A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947281 | ||||||
| chr2:170947368
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(19): Show | 24 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-982T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947368 | ||||||
| chr2:170947382
|
A | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0063others(10): Show | 18 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-968A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947382 | ||||||
| chr2:170947396
|
C | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.64-954C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947396 | ||||||
| chr2:170947413
|
A | G | 2 | a0001c0003t0001g0047a0007c0008t0001g0049 | 2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.64-937A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947413 | ||||||
| chr2:170947452
|
T | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.64-898T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947452 | ||||||
| chr2:170947468
|
C | T | 2 | a0001c0003t0001g0020a0003c0004t0001g0038 | 3 | HG02970.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-882C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947468 | ||||||
| chr2:170947507
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-843C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947507 | ||||||
| chr2:170947592
|
C | T | 6 | a0002c0002t0001g0198a0002c0002t0001g0233a0002c0002t0001g0234others(3): Show | 6 | HG00642.hp1 HG00741.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-758C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947592 | ||||||
| chr2:170947739
|
C | T | 1 | a0001c0003t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-611C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947739 | ||||||
| chr2:170947992
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0244 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.64-358G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170947992 | ||||||
| chr2:170948143
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-207A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170948143 | ||||||
| chr2:170948153
|
G | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0093others(2): Show | 5 | HG00140.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-197G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 1/9 | chr2 | 170948153 | ||||||
| chr2:170948459
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.144+29A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948459 | ||||||
| chr2:170948557
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.144+127A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948557 | ||||||
| chr2:170948628
|
A | C | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.144+198A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948628 | ||||||
| chr2:170948925
|
G | A | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.144+495G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170948925 | ||||||
| chr2:170949275
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.145-264A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949275 | ||||||
| chr2:170949360
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.145-179G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949360 | ||||||
| chr2:170949413
|
T | A | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.145-126T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 2/9 | chr2 | 170949413 | ||||||
| chr2:170949806
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.348+64A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170949806 | ||||||
| chr2:170949939
|
T | C | 5 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+197T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170949939 | ||||||
| chr2:170950109
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0129 | 2 | HG00609.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.349-95A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950109 | ||||||
| chr2:170950113
|
A | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-91A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950113 | ||||||
| chr2:170950134
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.349-70A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 3/9 | chr2 | 170950134 | ||||||
| chr2:170950407
|
C | G | 7 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+117C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950407 | ||||||
| chr2:170950494
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.435+204C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950494 | ||||||
| chr2:170950557
|
A | G | 1 | a0001c0003t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.435+267A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950557 | ||||||
| chr2:170950843
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0025others(8): Show | 19 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.436-485A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950843 | ||||||
| chr2:170950933
|
A | T | 1 | a0001c0001t0001g0012 | 3 | HG02809.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.436-395A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950933 | ||||||
| chr2:170950974
|
A | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.436-354A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170950974 | ||||||
| chr2:170951127
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436-201A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170951127 | ||||||
| chr2:170951141
|
G | A | 3 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0252 | 3 | NA18962.hp1 NA19055.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.436-187G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 4/9 | chr2 | 170951141 | ||||||
| chr2:170951502
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+44C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951502 | ||||||
| chr2:170951617
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.566+159T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951617 | ||||||
| chr2:170951710
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00099.hp1 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+252A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951710 | ||||||
| chr2:170951717
|
C | T | 1 | a0001c0003t0001g0047 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.566+259C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951717 | ||||||
| chr2:170951890
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0115 | 2 | HG02602.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.566+432G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951890 | ||||||
| chr2:170951894
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.566+436C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170951894 | ||||||
| chr2:170952115
|
C | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(31): Show | 45 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.566+657C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952115 | ||||||
| chr2:170952306
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.566+848C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952306 | ||||||
| chr2:170952608
|
T | A | 3 | a0001c0003t0002g0071a0001c0003t0002g0072a0001c0003t0002g0073 | 3 | HG01081.hp2 HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.566+1150T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952608 | ||||||
| chr2:170952751
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566+1293C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952751 | ||||||
| chr2:170952893
|
C | G | 2 | a0001c0003t0001g0007a0001c0003t0001g0048 | 6 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+1435C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952893 | ||||||
| chr2:170952915
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566+1457A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952915 | ||||||
| chr2:170952975
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.566+1517C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170952975 | ||||||
| chr2:170953179
|
A | G | 2 | a0001c0003t0001g0007a0001c0003t0001g0048 | 6 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-1471A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953179 | ||||||
| chr2:170953192
|
CAAAAAAT others(3): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567-1453_567-1444d others(12): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953192 | |||||
| chr2:170953233
|
A | G | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.567-1417A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953233 | ||||||
| chr2:170953259
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.567-1391G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953259 | ||||||
| chr2:170953261
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.567-1389C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953261 | ||||||
| chr2:170953278
|
C | T | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-1372C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953278 | ||||||
| chr2:170953333
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.567-1317G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953333 | ||||||
| chr2:170953355
|
T | TAATA | 11 | a0001c0001t0001g0057a0001c0003t0001g0020a0001c0003t0001g0066others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-1268_567-1265d others(6): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | |||||
| chr2:170953355
|
T | TAATAAAT others(5): Show |
2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.567-1276_567-1265d others(14): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | |||||
| chr2:170953355
|
TAATA | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.567-1268_567-1265d others(6): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170953355 | |||||
| chr2:170953513
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.567-1137G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953513 | ||||||
| chr2:170953532
|
T | C | 1 | a0001c0003t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.567-1118T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953532 | ||||||
| chr2:170953597
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG01106.hp1 HG01243.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.567-1053G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953597 | ||||||
| chr2:170953901
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(33): Show | 57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.567-749A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953901 | ||||||
| chr2:170953946
|
G | A | 30 | a0002c0002t0001g0005a0002c0002t0001g0130a0002c0002t0001g0191others(27): Show | 35 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.567-704G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953946 | ||||||
| chr2:170953988
|
C | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.567-662C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170953988 | ||||||
| chr2:170954222
|
G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.567-428G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954222 | ||||||
| chr2:170954333
|
G | A | 1 | a0001c0003t0001g0020 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.567-317G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954333 | ||||||
| chr2:170954351
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.567-299A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954351 | ||||||
| chr2:170954530
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-120G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954530 | ||||||
| chr2:170954538
|
T | C | 2 | a0002c0002t0001g0227a0002c0002t0001g0228 | 2 | NA19001.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.567-112T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954538 | ||||||
| chr2:170954647
|
T | A | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.567-3T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 5/9 | chr2 | 170954647 | ||||||
| chr2:170954887
|
G | A | 1 | a0002c0002t0001g0221 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.699+105G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170954887 | ||||||
| chr2:170955036
|
T | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.699+254T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170955036 | ||||||
| chr2:170955558
|
A | G | 1 | a0002c0002t0001g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.699+776A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170955558 | ||||||
| chr2:170956151
|
A | C | 1 | a0001c0001t0001g0267 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.700-285A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 6/9 | chr2 | 170956151 | ||||||
| chr2:170956742
|
TAAA | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.823+193_823+195del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170956742 | |||||
| chr2:170956806
|
C | T | 2 | a0002c0002t0001g0214a0002c0002t0001g0215 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.823+247C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956806 | ||||||
| chr2:170956929
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.823+370T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956929 | ||||||
| chr2:170956932
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0058 | 3 | HG02886.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823+373T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170956932 | ||||||
| chr2:170957148
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.823+589T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957148 | ||||||
| chr2:170957178
|
C | T | 1 | a0001c0003t0001g0047 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.823+619C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957178 | ||||||
| chr2:170957199
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0204 | 3 | HG02257.hp2 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.823+640A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957199 | ||||||
| chr2:170957240
|
C | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0112a0001c0001t0001g0129others(3): Show | 6 | HG00323.hp2 HG00609.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+681C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957240 | ||||||
| chr2:170957371
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.823+812A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957371 | ||||||
| chr2:170957578
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02602.hp2 HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.823+1019C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957578 | ||||||
| chr2:170957704
|
A | T | 1 | a0002c0002t0001g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823+1145A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957704 | ||||||
| chr2:170957743
|
A | C | 1 | a0002c0002t0001g0228 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.823+1184A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957743 | ||||||
| chr2:170957916
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.823+1357C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957916 | ||||||
| chr2:170957946
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+1387A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957946 | ||||||
| chr2:170957965
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823+1406A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170957965 | ||||||
| chr2:170958128
|
C | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1569C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958128 | ||||||
| chr2:170958181
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0244 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.823+1622C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958181 | ||||||
| chr2:170958240
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.823+1681C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958240 | ||||||
| chr2:170958380
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(25): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.823+1821A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958380 | ||||||
| chr2:170958653
|
CT | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(19): Show | 25 | HG01069.hp1 HG01081.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.823+2115delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958653 | |||||
| chr2:170958653
|
CTT | C | 6 | a0001c0001t0001g0040a0001c0003t0001g0133a0001c0003t0001g0148others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2114_823+2115d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958653 | |||||
| chr2:170958674
|
T | A | 2 | a0001c0003t0001g0050a0007c0008t0001g0049 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.823+2115T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958674 | ||||||
| chr2:170958674
|
TA | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0098a0001c0001t0001g0110others(12): Show | 15 | HG00408.hp2 HG00621.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.823+2129delA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | |||||
| chr2:170958674
|
TAA | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.823+2128_823+2129d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | |||||
| chr2:170958674
|
TAAA | T | 21 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0081others(18): Show | 23 | HG00323.hp2 HG01081.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+2127_823+2129d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170958674 | |||||
| chr2:170958675
|
A | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(18): Show | 32 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.823+2116A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958675 | ||||||
| chr2:170958676
|
A | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(29): Show | 43 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.823+2117A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958676 | ||||||
| chr2:170958677
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.823+2118A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958677 | ||||||
| chr2:170958678
|
A | T | 8 | a0001c0001t0001g0264a0001c0001t0001g0265a0002c0002t0001g0188others(5): Show | 11 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+2119A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958678 | ||||||
| chr2:170958684
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.823+2125A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958684 | ||||||
| chr2:170958810
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.823+2251C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958810 | ||||||
| chr2:170958851
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.823+2292G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958851 | ||||||
| chr2:170958913
|
G | A | 7 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+2354G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958913 | ||||||
| chr2:170958966
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0115 | 2 | HG02602.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.823+2407G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170958966 | ||||||
| chr2:170959023
|
C | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2464C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959023 | ||||||
| chr2:170959058
|
T | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2499T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959058 | ||||||
| chr2:170959063
|
C | T | 6 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0001g0280others(3): Show | 6 | HG00408.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2504C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959063 | ||||||
| chr2:170959085
|
C | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2526C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959085 | ||||||
| chr2:170959093
|
T | G | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2534T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959093 | ||||||
| chr2:170959094
|
G | T | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2535G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959094 | ||||||
| chr2:170959095
|
G | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823+2536G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959095 | ||||||
| chr2:170959219
|
C | T | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2444C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959219 | ||||||
| chr2:170959260
|
C | G | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2403C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959260 | ||||||
| chr2:170959306
|
A | C | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2357A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959306 | ||||||
| chr2:170959316
|
T | A | 1 | a0002c0002t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-2347T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959316 | ||||||
| chr2:170959522
|
G | C | 10 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(7): Show | 11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-2141G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959522 | ||||||
| chr2:170959594
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-2069A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959594 | ||||||
| chr2:170959610
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(17): Show | 26 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-2053A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959610 | ||||||
| chr2:170959722
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.824-1941G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959722 | ||||||
| chr2:170959787
|
C | G | 1 | a0001c0003t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.824-1876C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959787 | ||||||
| chr2:170959821
|
C | CT | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.824-1824dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170959821 | |||||
| chr2:170959860
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.824-1803C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170959860 | ||||||
| chr2:170960021
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.824-1642A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960021 | ||||||
| chr2:170960057
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG01346.hp1 HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.824-1606G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960057 | ||||||
| chr2:170960077
|
T | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1586T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960077 | ||||||
| chr2:170960086
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.824-1577G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960086 | ||||||
| chr2:170960091
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0140 | 2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.824-1572G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960091 | ||||||
| chr2:170960141
|
A | G | 2 | a0002c0002t0001g0036a0002c0002t0001g0193 | 3 | HG02155.hp2 NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.824-1522A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960141 | ||||||
| chr2:170960214
|
C | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.824-1449C>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960214 | ||||||
| chr2:170960247
|
A | G | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.824-1416A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960247 | ||||||
| chr2:170960258
|
T | G | 5 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG04199.hp2 NA18954.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-1405T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960258 | ||||||
| chr2:170960361
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.824-1302T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960361 | ||||||
| chr2:170960442
|
T | C | 1 | a0001c0003t0002g0021 | 2 | HG01069.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.824-1221T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960442 | ||||||
| chr2:170960564
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0276a0001c0001t0001g0284 | 5 | NA18940.hp2 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1099C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960564 | ||||||
| chr2:170960788
|
G | C | 3 | a0001c0003t0001g0133a0001c0003t0001g0148a0001c0003t0001g0190 | 3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.824-875G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960788 | ||||||
| chr2:170960989
|
G | A | 3 | a0001c0003t0001g0133a0001c0003t0001g0148a0001c0003t0001g0190 | 3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.824-674G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170960989 | ||||||
| chr2:170961162
|
C | T | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0040others(21): Show | 27 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.824-501C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961162 | ||||||
| chr2:170961284
|
C | T | 1 | a0003c0004t0001g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.824-379C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961284 | ||||||
| chr2:170961302
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.824-361G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961302 | ||||||
| chr2:170961403
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.824-260C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961403 | ||||||
| chr2:170961415
|
CTGG | C | 10 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(7): Show | 11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-247_824-245del others(3): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961415 | ||||||
| chr2:170961418
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.824-245G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961418 | ||||||
| chr2:170961419
|
G | C | 10 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(7): Show | 11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-244G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961419 | ||||||
| chr2:170961619
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0244 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.824-44C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 7/9 | chr2 | 170961619 | ||||||
| chr2:170961776
|
G | T | 1 | a0001c0003t0001g0020 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.910+27G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961776 | ||||||
| chr2:170961779
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.910+30G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961779 | ||||||
| chr2:170961998
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 5 | HG01074.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+249A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170961998 | ||||||
| chr2:170962020
|
C | G | 3 | a0001c0003t0001g0133a0001c0003t0001g0148a0001c0003t0001g0190 | 3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.910+271C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962020 | ||||||
| chr2:170962079
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.910+330A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962079 | ||||||
| chr2:170962087
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.910+338T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962087 | ||||||
| chr2:170962091
|
C | T | 1 | a0002c0002t0001g0035 | 2 | NA18612.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.910+342C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962091 | ||||||
| chr2:170962236
|
A | C | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.910+487A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962236 | ||||||
| chr2:170962490
|
A | G | 2 | a0001c0001t0003g0125a0001c0001t0003g0175 | 2 | HG00733.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.911-349A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 8/9 | chr2 | 170962490 | ||||||
| chr2:170962979
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 9 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018+33C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170962979 | ||||||
| chr2:170963355
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(19): Show | 33 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1018+409A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963355 | ||||||
| chr2:170963374
|
C | CA | 29 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 31 | HG00438.hp2 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1018+445dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963374 | |||||
| chr2:170963426
|
GCTGCTA | G | 10 | a0001c0001t0001g0017a0001c0003t0001g0020a0001c0003t0001g0066others(7): Show | 13 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018+486_1018+491d others(8): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963426 | |||||
| chr2:170963431
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 6 | HG02615.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018+485T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963431 | ||||||
| chr2:170963432
|
A | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 14 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1018+486A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963432 | ||||||
| chr2:170963447
|
G | C | 2 | a0001c0003t0001g0183a0001c0003t0001g0184 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1018+501G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963447 | ||||||
| chr2:170963450
|
G | C | 11 | a0001c0003t0001g0020a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018+504G>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963450 | ||||||
| chr2:170963450
|
G | GCTC | 48 | a0002c0002t0001g0005a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1018+524_1018+526d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963450 | |||||
| chr2:170963453
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1018+507C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963453 | ||||||
| chr2:170963462
|
C | G | 1 | a0001c0001t0001g0031 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1018+516C>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963462 | ||||||
| chr2:170963469
|
CT | C | 6 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018+524delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963469 | ||||||
| chr2:170963470
|
T | C | 5 | a0001c0003t0001g0020a0001c0003t0001g0078a0001c0003t0001g0183others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+524T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963470 | ||||||
| chr2:170963470
|
T | TC | 14 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0077others(11): Show | 14 | HG00621.hp2 HG01192.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1018+529dupC | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963470 | |||||
| chr2:170963473
|
C | CCCTCCT | 7 | a0001c0001t0001g0037a0001c0001t0001g0275a0001c0001t0001g0278others(4): Show | 8 | HG00140.hp2 HG00642.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+536_1018+541d others(8): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963473 | |||||
| chr2:170963473
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1018+527C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963473 | ||||||
| chr2:170963476
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1018+530T>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963476 | ||||||
| chr2:170963488
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1018+542C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963488 | ||||||
| chr2:170963523
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1018+577A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963523 | ||||||
| chr2:170963775
|
T | A | 1 | a0001c0003t0001g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1018+829T>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963775 | ||||||
| chr2:170963960
|
T | TA | 30 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(27): Show | 41 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1018+1024dupA | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170963960 | |||||
| chr2:170963980
|
A | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(33): Show | 57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1018+1034A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170963980 | ||||||
| chr2:170964017
|
C | T | 1 | a0007c0008t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1018+1071C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964017 | ||||||
| chr2:170964426
|
G | GT | 3 | a0001c0003t0001g0133a0001c0003t0001g0148a0001c0003t0001g0190 | 3 | HG02630.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1019-1363dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964426 | |||||
| chr2:170964574
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1019-1216A>C | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964574 | ||||||
| chr2:170964607
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1019-1183C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964607 | ||||||
| chr2:170964608
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(26): Show | 40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1019-1182G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964608 | ||||||
| chr2:170964623
|
A | T | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-1167A>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964623 | ||||||
| chr2:170964635
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1019-1155A>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964635 | ||||||
| chr2:170964716
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1019-1074G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964716 | ||||||
| chr2:170964883
|
T | G | 4 | a0002c0002t0001g0211a0002c0002t0001g0221a0002c0002t0001g0222others(1): Show | 4 | NA18980.hp2 NA18985.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019-907T>G | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170964883 | ||||||
| chr2:170964892
|
A | AT | 27 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0065others(24): Show | 28 | HG00140.hp2 HG01081.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.1019-871dupT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | |||||
| chr2:170964892
|
A | ATT | 26 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0024others(23): Show | 37 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1019-872_1019-871d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | |||||
| chr2:170964892
|
A | ATTT | 9 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0058others(6): Show | 9 | HG01175.hp1 HG01433.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1019-873_1019-871d others(5): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | |||||
| chr2:170964892
|
AT | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(85): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1019-871delT | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | |||||
| chr2:170964892
|
ATT | A | 51 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0061others(48): Show | 65 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1019-872_1019-871d others(4): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170964892 | |||||
| chr2:170965067
|
C | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0193 | 3 | HG02155.hp2 NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1019-723C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965067 | ||||||
| chr2:170965082
|
TGTACTTT others(26): Show |
T | 1 | a0002c0002t0001g0130 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1019-707_1019-675d others(35): Show |
GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965082 | ||||||
| chr2:170965323
|
C | T | 1 | a0001c0006t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1019-467C>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965323 | ||||||
| chr2:170965425
|
G | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1019-365G>T | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965425 | ||||||
| chr2:170965428
|
TG | T | 54 | a0002c0002t0001g0005a0002c0002t0001g0009a0002c0002t0001g0010others(51): Show | 68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1019-359delG | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 170965428 | |||||
| chr2:170965609
|
G | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1019-181G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965609 | ||||||
| chr2:170965755
|
G | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-35G>A | GORASP2 | ENSG00000115806.13 | transcript | ENST00000234160.5 | protein_coding | 9/9 | chr2 | 170965755 |