Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54873 |
|---|---|
| ensemblid | ENSG00000099260.12 |
| hgncid | 15846 |
| symbol | PALMD |
| name | palmdelphin |
| refseq_nuc | NM_017734.5 |
| refseq_prot | NP_060204.1 |
| ensembl_nuc | ENST00000263174.9 |
| ensembl_prot | ENSP00000263174.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 99646113 |
| end | 99694535 |
| strand | + |
| ver | v1.2 |
| region | chr1:99646113-99694535 |
| region5000 | chr1:99641113-99699535 |
| regionname0 | PALMD_chr1_99646113_99694535 |
| regionname5000 | PALMD_chr1_99641113_99699535 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 551 | 356 | 76 | 66 | 162 | 12 | 38 | 122 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0002 | 0/0 | 551 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0003 | 0/0 | 551 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0004 | 0/0 | 551 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0005 | 0/0 | 551 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0006 | 0/0 | 551 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0007 | 0/0 | 551 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0008 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0009 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0010 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0011 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1656 | 330 | 55 | 65 | 161 | 12 | 35 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0002 | 0/0 | 1656 | 21 | 16 | 1 | 1 | 0 | 3 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0003 | 0/0 | 1656 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0004 | 0/0 | 1656 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0005 | 0/0 | 1656 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0006 | 0/0 | 1656 | 3 | 2 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0007 | 0/0 | 1656 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0008 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0009 | 0/0 | 1656 | 2 | 0 | 1 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0010 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0011 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0012 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0013 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0014 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| c0015 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 679 | 358 | 77 | 70 | 158 | 12 | 39 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0002 | 0/0 | 676 | 13 | 13 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0003 | 0/0 | 679 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0004 | 0/0 | 679 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0005 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0006 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0007 | 0/0 | 679 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| t0008 | 0/0 | 679 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1656 | 330 | 55 | 65 | 161 | 12 | 35 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0002 | 0/0 | 1656 | 21 | 16 | 1 | 1 | 0 | 3 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0005 | 0/0 | 1656 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0012 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0002c0003 | 0/0 | 1656 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0002c0008 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0003c0004 | 0/0 | 1656 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0004c0006 | 0/0 | 1656 | 3 | 2 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0005c0009 | 0/0 | 1656 | 2 | 0 | 1 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0006c0007 | 0/0 | 1656 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0007c0011 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0008c0013 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0009c0010 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0010c0014 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0011c0015 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2334 | 321 | 51 | 65 | 157 | 12 | 34 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0002 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0003 | 0/0 | 2334 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0004 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0006 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0007 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0001t0008 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0002t0001 | 0/0 | 2334 | 10 | 5 | 1 | 1 | 0 | 3 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0002t0002 | 0/0 | 2331 | 11 | 11 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0005t0001 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0001c0012t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0002c0003t0001 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0002c0008t0001 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0003c0004t0001 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0003c0004t0005 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0004c0006t0001 | 0/0 | 2334 | 3 | 2 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0005c0009t0001 | 0/0 | 2334 | 2 | 0 | 1 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0006c0007t0001 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0007c0011t0001 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0008c0013t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0009c0010t0002 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0010c0014t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| a0011c0015t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | copy fasta | chr1 | 99641113 | 99699535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0012t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0008t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0008t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0005c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0005c0009t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0006c0007t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0006c0007t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0007c0011t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0008c0013t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0009c0010t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0010c0014t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0011c0015t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0349 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00735 | hp1 | a0004 | c0006 | t0001 | g0309 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01167 | hp2 | a0005 | c0009 | t0001 | g0012 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01256 | hp1 | a0006 | c0007 | t0001 | g0328 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01258 | hp1 | a0006 | c0007 | t0001 | g0329 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0369 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02145 | hp1 | a0002 | c0008 | t0001 | g0279 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02258 | hp1 | a0011 | c0015 | t0001 | g0139 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0303 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0162 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02622 | hp2 | a0003 | c0004 | t0005 | g0242 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02717 | hp2 | a0010 | c0014 | t0001 | g0271 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02723 | hp1 | a0001 | c0012 | t0001 | g0258 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0002 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0353 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0354 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0355 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0352 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0304 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0296 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0229 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0302 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0307 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03195 | hp1 | a0002 | c0008 | t0001 | g0264 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0081 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0368 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03516 | hp1 | a0008 | c0013 | t0001 | g0344 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0241 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03654 | hp2 | a0007 | c0011 | t0001 | g0013 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0168 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03927 | hp2 | a0005 | c0009 | t0001 | g0011 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19043 | hp1 | a0003 | c0004 | t0001 | g0002 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0002 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0358 | AFR | ASW | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0356 | AFR | ASW | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | TSI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0312 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02109 | hp2 | a0004 | c0006 | t0001 | g0310 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0362 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03471 | hp2 | a0009 | c0010 | t0002 | g0364 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0171 | REF | REF | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0278 | REF | REF | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99667693
|
G | C | 1 | a0006 | 2 | HG01256.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.178G>C | p.Glu60Gln | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/8 | 383/2334 | 178/1656 | 60/551 | chr1 | 99667693 | ||
| chr1:99667734
|
C | A | 2 | a0002a0004 | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
missense_variant | MODERATE | c.219C>A | p.His73Gln | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/8 | 424/2334 | 219/1656 | 73/551 | chr1 | 99667734 | ||
| chr1:99686777
|
A | G | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.353A>G | p.Glu118Gly | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/8 | 558/2334 | 353/1656 | 118/551 | chr1 | 99686777 | ||
| chr1:99688946
|
A | G | 1 | a0010 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.686A>G | p.Asn229Ser | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 891/2334 | 686/1656 | 229/551 | chr1 | 99688946 | ||
| chr1:99688954
|
G | A | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.694G>A | p.Asp232Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 899/2334 | 694/1656 | 232/551 | chr1 | 99688954 | ||
| chr1:99689087
|
C | T | 1 | a0005 | 2 | HG01167.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.827C>T | p.Thr276Met | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1032/2334 | 827/1656 | 276/551 | chr1 | 99689087 | ||
| chr1:99689209
|
T | C | 1 | a0008 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.949T>C | p.Phe317Leu | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1154/2334 | 949/1656 | 317/551 | chr1 | 99689209 | ||
| chr1:99689637
|
G | T | 2 | a0002a0003 | 12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
missense_variant | MODERATE | c.1377G>T | p.Glu459Asp | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1582/2334 | 1377/1656 | 459/551 | chr1 | 99689637 | ||
| chr1:99689795
|
G | A | 1 | a0007 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1535G>A | p.Ser512Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1740/2334 | 1535/1656 | 512/551 | chr1 | 99689795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99688911
|
G | A | 7 | a0001c0002a0002c0003a0002c0008others(4): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
synonymous_variant | LOW | c.651G>A | p.Val217Val | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 856/2334 | 651/1656 | 217/551 | chr1 | 99688911 | ||
| chr1:99688998
|
C | A | 1 | a0001c0012 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.738C>A | p.Ala246Ala | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 943/2334 | 738/1656 | 246/551 | chr1 | 99688998 | ||
| chr1:99689076
|
A | T | 1 | a0001c0005 | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.816A>T | p.Pro272Pro | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1021/2334 | 816/1656 | 272/551 | chr1 | 99689076 | ||
| chr1:99689766
|
T | C | 1 | a0002c0008 | 2 | HG02145.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1506T>C | p.Asn502Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1711/2334 | 1506/1656 | 502/551 | chr1 | 99689766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99646146
|
C | A | 1 | a0001c0001t0003 | 3 | NA19010.hp1 NA19012.hp1 NA19056.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-172C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/8 | chr1 | 99646146 | ||||||
| chr1:99646201
|
A | G | 1 | a0001c0001t0008 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-117A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/8 | 117 | chr1 | 99646201 | |||||
| chr1:99694129
|
T | C | 1 | a0003c0004t0005 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 67 | chr1 | 99694129 | |||||
| chr1:99694158
|
C | A | 1 | a0001c0001t0006 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 96 | chr1 | 99694158 | |||||
| chr1:99694481
|
T | C | 1 | a0001c0001t0004 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*419T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 419 | chr1 | 99694481 | |||||
| chr1:99694499
|
T | C | 1 | a0001c0001t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 437 | chr1 | 99694499 | |||||
| chr1:99694523
|
ATCC | A | 3 | a0001c0001t0002a0001c0002t0002a0009c0010t0002 | 13 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*468delCCT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 466 | INFO_REALIGN_3_PRIME | chr1 | 99694523 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99646400
|
A | G | 72 | a0001c0001t0001g0008a0001c0001t0001g0301a0001c0001t0001g0308others(69): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.45+38A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646400 | ||||||
| chr1:99646515
|
C | T | 1 | a0001c0001t0001g0370 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+153C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646515 | ||||||
| chr1:99646637
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.45+275T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646637 | ||||||
| chr1:99646731
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+369T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646731 | ||||||
| chr1:99646734
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+372T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646734 | ||||||
| chr1:99646875
|
C | T | 1 | a0001c0002t0002g0369 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+513C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646875 | ||||||
| chr1:99646917
|
G | A | 1 | a0001c0002t0001g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+555G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646917 | ||||||
| chr1:99647063
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0301others(4): Show | 7 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+701G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647063 | ||||||
| chr1:99647147
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG03927.hp1 NA18992.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.45+785G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647147 | ||||||
| chr1:99647180
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.45+818C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647180 | ||||||
| chr1:99647188
|
T | C | 9 | a0001c0001t0001g0308a0001c0002t0002g0305a0001c0002t0002g0306others(6): Show | 9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+826T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647188 | ||||||
| chr1:99647473
|
A | C | 9 | a0001c0001t0001g0308a0001c0002t0002g0305a0001c0002t0002g0306others(6): Show | 9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+1111A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647473 | ||||||
| chr1:99647842
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+1480G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647842 | ||||||
| chr1:99647873
|
G | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45+1511G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647873 | ||||||
| chr1:99647982
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+1620A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647982 | ||||||
| chr1:99648186
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.45+1824G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648186 | ||||||
| chr1:99648201
|
C | T | 2 | a0004c0006t0001g0309a0004c0006t0001g0310 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.45+1839C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648201 | ||||||
| chr1:99648554
|
A | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2192A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648554 | ||||||
| chr1:99648555
|
G | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2193G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648555 | ||||||
| chr1:99648576
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2214A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648576 | ||||||
| chr1:99648583
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.45+2221G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648583 | ||||||
| chr1:99648603
|
C | T | 9 | a0001c0001t0001g0020a0001c0001t0001g0240a0001c0001t0001g0243others(6): Show | 11 | HG02280.hp2 HG02622.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+2241C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648603 | ||||||
| chr1:99648660
|
GA | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0002t0001g0014others(4): Show | 7 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+2310delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648660 | |||||
| chr1:99648752
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.45+2390C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648752 | ||||||
| chr1:99648831
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.45+2469G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648831 | ||||||
| chr1:99648874
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.45+2512C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648874 | ||||||
| chr1:99648888
|
C | CA | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.45+2543dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | |||||
| chr1:99648888
|
C | CAA | 68 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 69 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.45+2542_45+2543dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | |||||
| chr1:99648888
|
CA | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0237others(6): Show | 9 | HG00323.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+2543delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | |||||
| chr1:99648952
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | NA18983.hp1 NA19066.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.45+2590T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648952 | ||||||
| chr1:99649076
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.45+2714G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649076 | ||||||
| chr1:99649083
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2721C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649083 | ||||||
| chr1:99649111
|
T | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.45+2749T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649111 | ||||||
| chr1:99649113
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.45+2751G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649113 | ||||||
| chr1:99649470
|
GAGAAGAG others(8): Show |
G | 1 | a0001c0002t0001g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+3114_45+3128del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99649470 | |||||
| chr1:99649476
|
A | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(283): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.45+3114A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649476 | ||||||
| chr1:99649500
|
A | C | 9 | a0001c0001t0001g0308a0001c0002t0002g0305a0001c0002t0002g0306others(6): Show | 9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+3138A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649500 | ||||||
| chr1:99649531
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.45+3169C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649531 | ||||||
| chr1:99649545
|
G | C | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0005t0001g0302others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3183G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649545 | ||||||
| chr1:99649581
|
G | A | 1 | a0011c0015t0001g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.45+3219G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649581 | ||||||
| chr1:99649768
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+3406C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649768 | ||||||
| chr1:99650004
|
A | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.45+3642A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650004 | ||||||
| chr1:99650048
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+3686G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650048 | ||||||
| chr1:99650062
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0246 | 3 | HG02895.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.45+3700A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650062 | ||||||
| chr1:99650094
|
G | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0002t0001g0014others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+3732G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650094 | ||||||
| chr1:99650285
|
G | GA | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0126others(23): Show | 26 | HG00408.hp2 HG00544.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+3957dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
G | GAA | 11 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0150others(8): Show | 11 | HG00621.hp1 HG01109.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3956_45+3957dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GA | G | 11 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(8): Show | 11 | HG02145.hp1 HG02717.hp1 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3957delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(4): Show |
G | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0287others(5): Show | 8 | HG01175.hp2 HG02738.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+3947_45+3957del others(11): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(5): Show |
G | 94 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0025others(91): Show | 97 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+3946_45+3957del others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0116 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.45+3945_45+3957del others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(7): Show |
G | 12 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0301others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+3944_45+3957del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(11): Show |
G | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45+3940_45+3957del others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(12): Show |
G | 50 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+3939_45+3957del others(19): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650285
|
GAAAAAAA others(13): Show |
G | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.45+3938_45+3957del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | |||||
| chr1:99650482
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+4120G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650482 | ||||||
| chr1:99650486
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(141): Show | 147 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.45+4124G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650486 | ||||||
| chr1:99650533
|
T | C | 11 | a0001c0001t0001g0308a0002c0003t0001g0081a0002c0003t0001g0229others(8): Show | 11 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+4171T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650533 | ||||||
| chr1:99650562
|
CT | C | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.45+4205delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650562 | |||||
| chr1:99650689
|
T | C | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45+4327T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650689 | ||||||
| chr1:99650697
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.45+4335G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650697 | ||||||
| chr1:99650838
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(240): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.45+4476C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650838 | ||||||
| chr1:99650839
|
G | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG01934.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+4477G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650839 | ||||||
| chr1:99650841
|
T | C | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+4479T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650841 | ||||||
| chr1:99651086
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(241): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.45+4724A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651086 | ||||||
| chr1:99651161
|
CCA | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(49): Show | 53 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+4802_45+4803del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99651161 | |||||
| chr1:99651207
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0140 | 3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+4845G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651207 | ||||||
| chr1:99651243
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+4881G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651243 | ||||||
| chr1:99651294
|
G | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(241): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.45+4932G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651294 | ||||||
| chr1:99651327
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.45+4965A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651327 | ||||||
| chr1:99651344
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.45+4982T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651344 | ||||||
| chr1:99651488
|
G | A | 6 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+5126G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651488 | ||||||
| chr1:99651892
|
T | C | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45+5530T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651892 | ||||||
| chr1:99651901
|
T | C | 18 | a0001c0001t0001g0160a0001c0001t0001g0237a0001c0001t0001g0361others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.45+5539T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651901 | ||||||
| chr1:99651969
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.45+5607C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651969 | ||||||
| chr1:99652055
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+5693T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652055 | ||||||
| chr1:99652160
|
T | C | 17 | a0001c0001t0001g0160a0001c0001t0001g0237a0001c0001t0004g0158others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+5798T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652160 | ||||||
| chr1:99652207
|
G | A | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+5845G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652207 | ||||||
| chr1:99652321
|
T | A | 1 | a0007c0011t0001g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+5959T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652321 | ||||||
| chr1:99652375
|
A | G | 4 | a0001c0001t0001g0350a0001c0001t0001g0361a0001c0002t0001g0313others(1): Show | 4 | HG02257.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6013A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652375 | ||||||
| chr1:99652465
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+6103A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652465 | ||||||
| chr1:99652481
|
G | C | 1 | a0001c0001t0001g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.45+6119G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652481 | ||||||
| chr1:99652494
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.45+6132C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652494 | ||||||
| chr1:99652551
|
C | G | 4 | a0001c0002t0002g0280a0001c0002t0002g0305a0001c0002t0002g0306others(1): Show | 4 | HG02723.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6189C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652551 | ||||||
| chr1:99652566
|
T | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6204T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652566 | ||||||
| chr1:99652587
|
G | C | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.45+6225G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652587 | ||||||
| chr1:99652599
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.45+6237G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652599 | ||||||
| chr1:99652618
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.45+6256G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652618 | ||||||
| chr1:99652626
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+6264A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652626 | ||||||
| chr1:99652659
|
A | AGAAAG | 25 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0087others(22): Show | 25 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+6332_45+6336dup others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
A | AGAAAGGA others(3): Show |
4 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG00408.hp2 HG02083.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6327_45+6336dup others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
A | AGAAAGGA others(8): Show |
3 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024 | 3 | HG01346.hp2 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.45+6322_45+6336dup others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
A | AGAAAGGA others(13): Show |
1 | a0001c0002t0001g0263 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.45+6317_45+6336dup others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
AGAAAG | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.45+6332_45+6336del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
AGAAAGGA others(3): Show |
A | 22 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0054others(19): Show | 22 | HG01167.hp2 HG01884.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+6327_45+6336del others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
AGAAAGGA others(8): Show |
A | 40 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0039others(37): Show | 41 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+6322_45+6336del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652659
|
AGAAAGGA others(13): Show |
A | 5 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6317_45+6336del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | |||||
| chr1:99652674
|
GGAAAGGA others(18): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+6317_45+6341del others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652674 | |||||
| chr1:99652679
|
GGAAAGGA others(13): Show |
G | 2 | a0001c0001t0001g0301a0001c0001t0001g0360 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.45+6322_45+6341del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652679 | |||||
| chr1:99652684
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0155 | 2 | HG01261.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.45+6322G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652684 | ||||||
| chr1:99652684
|
G | GGAAAAGA others(3): Show |
1 | a0001c0002t0002g0231 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+6326_45+6327ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652684 | |||||
| chr1:99652684
|
GGAAAGGA others(8): Show |
G | 3 | a0002c0003t0001g0353a0002c0003t0001g0354a0011c0015t0001g0139 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.45+6327_45+6341del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652684 | |||||
| chr1:99652689
|
G | A | 14 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0138others(11): Show | 14 | HG01261.hp2 HG01358.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+6327G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652689 | ||||||
| chr1:99652689
|
G | GGAAAAGA others(3): Show |
1 | a0002c0008t0001g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+6331_45+6332ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652689 | |||||
| chr1:99652689
|
G | GGAAAAGA others(18): Show |
1 | a0001c0001t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+6331_45+6332ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652689 | |||||
| chr1:99652694
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(94): Show | 99 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.45+6332G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652694 | ||||||
| chr1:99652694
|
G | GGAAAA | 40 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(37): Show | 43 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+6377_45+6381dup others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAAGA others(3): Show |
37 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0040others(34): Show | 38 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.45+6372_45+6381dup others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAAGA others(8): Show |
18 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(15): Show | 18 | HG00280.hp2 HG01358.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.45+6367_45+6381dup others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAAGA others(13): Show |
12 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0092others(9): Show | 12 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+6362_45+6381dup others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAAGA others(18): Show |
4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0091others(1): Show | 4 | HG01934.hp2 HG01975.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6357_45+6381dup others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAAGA others(23): Show |
1 | a0001c0001t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.45+6352_45+6381dup others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(3): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0243a0001c0001t0001g0350 | 3 | HG02886.hp2 HG03540.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.45+6336_45+6337ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(8): Show |
1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(13): Show |
1 | a0001c0001t0001g0105 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(18): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0249 | 2 | HG01978.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.45+6336_45+6337ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(33): Show |
1 | a0001c0001t0001g0102 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(23): Show |
1 | a0001c0001t0001g0119 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(13): Show |
1 | a0007c0011t0001g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
G | GGAAAGGA others(18): Show |
1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
GGAAAA | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01884.hp1 HG02735.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6377_45+6381del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652694
|
GGAAAAGA others(3): Show |
G | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.45+6372_45+6381del others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | |||||
| chr1:99652699
|
A | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0341a0001c0002t0001g0261others(1): Show | 4 | HG00140.hp1 HG00544.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6337A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652699 | ||||||
| chr1:99652704
|
A | G | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6342A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652704 | ||||||
| chr1:99652709
|
A | G | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6347A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652709 | ||||||
| chr1:99652711
|
AAAAGAAA others(22): Show |
A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG03540.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.45+6358_45+6386del others(29): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652711 | |||||
| chr1:99652714
|
A | G | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6352A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652714 | ||||||
| chr1:99652716
|
AAAAGAAA others(17): Show |
A | 2 | a0001c0001t0001g0010a0001c0001t0001g0196 | 2 | HG02886.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.45+6363_45+6386del others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652716 | |||||
| chr1:99652721
|
AAAAGAAA others(12): Show |
A | 8 | a0001c0001t0001g0118a0001c0001t0001g0197a0001c0001t0001g0255others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+6368_45+6386del others(19): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652721 | |||||
| chr1:99652726
|
AAAAGAAA others(7): Show |
A | 19 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(16): Show | 19 | HG00438.hp1 HG00673.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+6373_45+6386del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652726 | |||||
| chr1:99652731
|
AAAAGAAA others(2): Show |
A | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(29): Show | 34 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+6378_45+6386del others(9): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652731 | |||||
| chr1:99652736
|
AAAAG | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(54): Show | 58 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.45+6382_45+6385del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652736 | |||||
| chr1:99652740
|
G | GA | 31 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0130others(28): Show | 31 | HG00323.hp1 HG00621.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.45+6381dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652740
|
G | GAAAAGA | 13 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0149others(10): Show | 13 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652740
|
G | GAAAAGAA others(4): Show |
10 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG00597.hp2 HG01099.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(11): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652740
|
G | GAAAAGAA others(9): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652740
|
G | GAAAAGAA others(14): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG00423.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(21): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652740
|
G | GAAAAGAA others(24): Show |
1 | a0001c0001t0001g0190 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.45+6381_45+6382ins others(31): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | |||||
| chr1:99652811
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45+6449A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652811 | ||||||
| chr1:99652862
|
T | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0036others(38): Show | 42 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+6500T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652862 | ||||||
| chr1:99652879
|
T | C | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6517T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652879 | ||||||
| chr1:99652922
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6560G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652922 | ||||||
| chr1:99653017
|
C | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6655C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653017 | ||||||
| chr1:99653131
|
G | A | 2 | a0001c0002t0001g0313a0001c0002t0001g0362 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6769G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653131 | ||||||
| chr1:99653140
|
A | C | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6778A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653140 | ||||||
| chr1:99653161
|
AAACAAAA others(1): Show |
A | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6810_45+6817del others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99653161 | |||||
| chr1:99653211
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+6849T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653211 | ||||||
| chr1:99653256
|
G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.45+6894G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653256 | ||||||
| chr1:99653365
|
T | G | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+7003T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653365 | ||||||
| chr1:99653592
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.45+7230G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653592 | ||||||
| chr1:99653673
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.45+7311T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653673 | ||||||
| chr1:99653746
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.45+7384A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653746 | ||||||
| chr1:99653754
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.45+7392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653754 | ||||||
| chr1:99653904
|
C | T | 5 | a0001c0002t0002g0280a0001c0002t0002g0305a0001c0002t0002g0306others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+7542C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653904 | ||||||
| chr1:99653956
|
G | T | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.45+7594G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653956 | ||||||
| chr1:99654134
|
C | T | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+7772C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654134 | ||||||
| chr1:99654140
|
C | G | 2 | a0004c0006t0001g0309a0004c0006t0001g0310 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.45+7778C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654140 | ||||||
| chr1:99654146
|
C | T | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.45+7784C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654146 | ||||||
| chr1:99654334
|
TTAAA | T | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+7974_45+7977del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99654334 | |||||
| chr1:99654343
|
T | C | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7976T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654343 | ||||||
| chr1:99654344
|
AGCTATT | A | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7974_46-7969del others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654344 | ||||||
| chr1:99654451
|
G | A | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7868G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654451 | ||||||
| chr1:99654453
|
C | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.46-7866C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654453 | ||||||
| chr1:99654473
|
C | T | 3 | a0001c0001t0001g0361a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7846C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654473 | ||||||
| chr1:99654520
|
T | G | 6 | a0002c0008t0001g0264a0002c0008t0001g0279a0003c0004t0001g0002others(3): Show | 8 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-7799T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654520 | ||||||
| chr1:99654612
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.46-7707T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654612 | ||||||
| chr1:99654874
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7445C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654874 | ||||||
| chr1:99655071
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.46-7248C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655071 | ||||||
| chr1:99655168
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46-7151T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655168 | ||||||
| chr1:99655250
|
T | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7069T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655250 | ||||||
| chr1:99655260
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7059T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655260 | ||||||
| chr1:99655293
|
A | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7026A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655293 | ||||||
| chr1:99655309
|
T | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46-7010T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655309 | ||||||
| chr1:99655444
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-6875C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655444 | ||||||
| chr1:99655516
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6803G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655516 | ||||||
| chr1:99655553
|
C | A | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 5 | HG02257.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-6766C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655553 | ||||||
| chr1:99655715
|
G | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6604G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655715 | ||||||
| chr1:99655722
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-6597T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655722 | ||||||
| chr1:99655760
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6559G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655760 | ||||||
| chr1:99655787
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6532T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655787 | ||||||
| chr1:99655807
|
C | T | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.46-6512C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655807 | ||||||
| chr1:99655837
|
A | G | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-6482A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655837 | ||||||
| chr1:99655892
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6427C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655892 | ||||||
| chr1:99655898
|
G | A | 1 | a0001c0005t0001g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-6421G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655898 | ||||||
| chr1:99655927
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655927 | ||||||
| chr1:99655933
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.46-6386C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655933 | ||||||
| chr1:99655933
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6386C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655933 | ||||||
| chr1:99655933
|
CGCACACA others(9): Show |
C | 6 | a0001c0001t0001g0348a0001c0002t0001g0312a0001c0005t0001g0302others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-6370_46-6355del others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655933 | |||||
| chr1:99655936
|
ACACACAC others(7): Show |
A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.46-6370_46-6357del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655936 | |||||
| chr1:99655938
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0322 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46-6370_46-6359del others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655938 | |||||
| chr1:99655950
|
G | GCA | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-6353_46-6352dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655950 | |||||
| chr1:99656162
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.46-6157C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656162 | ||||||
| chr1:99656237
|
A | G | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(1): Show | 4 | HG01981.hp2 HG02602.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-6082A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656237 | ||||||
| chr1:99656287
|
G | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6032G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656287 | ||||||
| chr1:99656368
|
CTTTTT | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(49): Show | 54 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-5947_46-5943del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99656368 | |||||
| chr1:99656783
|
C | A | 1 | a0001c0002t0002g0231 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-5536C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656783 | ||||||
| chr1:99656792
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-5527A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656792 | ||||||
| chr1:99656921
|
C | T | 1 | a0001c0001t0001g0359 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46-5398C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656921 | ||||||
| chr1:99657044
|
G | T | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-5275G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657044 | ||||||
| chr1:99657240
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46-5079T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657240 | ||||||
| chr1:99657267
|
C | A | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-5052C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657267 | ||||||
| chr1:99657357
|
T | C | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-4962T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657357 | ||||||
| chr1:99657515
|
CCTAA | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4801_46-4798del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99657515 | |||||
| chr1:99657602
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.46-4717C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657602 | ||||||
| chr1:99657731
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4588C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657731 | ||||||
| chr1:99657782
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.46-4537G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657782 | ||||||
| chr1:99657809
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4510T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657809 | ||||||
| chr1:99657939
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4380C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657939 | ||||||
| chr1:99658116
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.46-4203C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658116 | ||||||
| chr1:99658303
|
C | CA | 11 | a0001c0001t0001g0021a0001c0001t0001g0083a0001c0001t0001g0118others(8): Show | 11 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-4001dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658303 | |||||
| chr1:99658303
|
CA | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(65): Show | 70 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.46-4001delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658303 | |||||
| chr1:99658347
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.46-3972A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658347 | ||||||
| chr1:99658519
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.46-3800C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658519 | ||||||
| chr1:99658628
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3691G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658628 | ||||||
| chr1:99658739
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-3580C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658739 | ||||||
| chr1:99658896
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3423T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658896 | ||||||
| chr1:99658902
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(62): Show | 67 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.46-3417T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658902 | ||||||
| chr1:99658921
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.46-3398C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658921 | ||||||
| chr1:99658945
|
C | CA | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(4): Show | 7 | HG02015.hp2 HG02055.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3360dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658945 | |||||
| chr1:99659137
|
A | G | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-3182A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659137 | ||||||
| chr1:99659510
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-2809T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659510 | ||||||
| chr1:99659565
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0036others(38): Show | 42 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-2754C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659565 | ||||||
| chr1:99659711
|
A | G | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-2608A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659711 | ||||||
| chr1:99659885
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-2434C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659885 | ||||||
| chr1:99660034
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.46-2285G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660034 | ||||||
| chr1:99660105
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-2214T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660105 | ||||||
| chr1:99660149
|
C | T | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-2170C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660149 | ||||||
| chr1:99660337
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1982C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660337 | ||||||
| chr1:99660343
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1976T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660343 | ||||||
| chr1:99660403
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-1916G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660403 | ||||||
| chr1:99660536
|
G | A | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-1783G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660536 | ||||||
| chr1:99660639
|
AT | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.46-1670delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99660639 | |||||
| chr1:99660690
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-1629A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660690 | ||||||
| chr1:99660746
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.46-1573C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660746 | ||||||
| chr1:99660901
|
A | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1418A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660901 | ||||||
| chr1:99660981
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.46-1338T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660981 | ||||||
| chr1:99661105
|
C | T | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-1214C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661105 | ||||||
| chr1:99661291
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.46-1028A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661291 | ||||||
| chr1:99661371
|
T | G | 1 | a0001c0002t0002g0369 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.46-948T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661371 | ||||||
| chr1:99661525
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-794G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661525 | ||||||
| chr1:99661678
|
G | C | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46-641G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661678 | ||||||
| chr1:99661728
|
A | G | 2 | a0006c0007t0001g0328a0006c0007t0001g0329 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.46-591A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661728 | ||||||
| chr1:99661799
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0140 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-520A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661799 | ||||||
| chr1:99661833
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-486G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661833 | ||||||
| chr1:99661928
|
G | A | 13 | a0001c0001t0001g0160a0001c0001t0001g0237a0001c0001t0006g0157others(10): Show | 13 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-391G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661928 | ||||||
| chr1:99661929
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0107others(1): Show | 4 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-390C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661929 | ||||||
| chr1:99661989
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.46-330C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661989 | ||||||
| chr1:99662062
|
A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(64): Show | 69 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.46-257A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99662062 | ||||||
| chr1:99662285
|
A | T | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-34A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99662285 | ||||||
| chr1:99662532
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+133T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662532 | ||||||
| chr1:99662563
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+164A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662563 | ||||||
| chr1:99662609
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+210T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662609 | ||||||
| chr1:99662779
|
G | A | 7 | a0001c0001t0001g0237a0001c0002t0001g0014a0001c0002t0001g0024others(4): Show | 7 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+380G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662779 | ||||||
| chr1:99662819
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+420T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662819 | ||||||
| chr1:99662830
|
T | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+431T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662830 | ||||||
| chr1:99663026
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+627G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663026 | ||||||
| chr1:99663036
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+637A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663036 | ||||||
| chr1:99663119
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.126+720C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663119 | ||||||
| chr1:99663150
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.126+751G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663150 | ||||||
| chr1:99663227
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(266): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.126+828A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663227 | ||||||
| chr1:99663434
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.126+1035A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663434 | ||||||
| chr1:99663520
|
C | T | 1 | a0002c0003t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.126+1121C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663520 | ||||||
| chr1:99663654
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1255C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663654 | ||||||
| chr1:99663779
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+1380G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663779 | ||||||
| chr1:99664018
|
G | C | 3 | a0001c0001t0004g0158a0001c0001t0004g0159a0008c0013t0001g0344 | 3 | HG02055.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.126+1619G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664018 | ||||||
| chr1:99664151
|
A | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1752A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664151 | ||||||
| chr1:99664158
|
G | T | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.126+1759G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664158 | ||||||
| chr1:99664251
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+1852T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664251 | ||||||
| chr1:99664308
|
G | A | 1 | a0008c0013t0001g0344 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+1909G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664308 | ||||||
| chr1:99664488
|
T | C | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126+2089T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664488 | ||||||
| chr1:99664556
|
G | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2157G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664556 | ||||||
| chr1:99664594
|
T | G | 15 | a0001c0001t0001g0160a0001c0001t0001g0237a0001c0001t0006g0157others(12): Show | 15 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+2195T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664594 | ||||||
| chr1:99664611
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2212A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664611 | ||||||
| chr1:99664791
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0115 | 3 | NA18984.hp2 NA18986.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.126+2392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664791 | ||||||
| chr1:99664992
|
A | T | 8 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2593A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664992 | ||||||
| chr1:99665088
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.127-2554G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665088 | ||||||
| chr1:99665125
|
T | C | 7 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0137others(4): Show | 7 | HG00408.hp2 HG00609.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2517T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665125 | ||||||
| chr1:99665154
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.127-2488A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665154 | ||||||
| chr1:99665391
|
G | A | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-2251G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665391 | ||||||
| chr1:99665404
|
T | C | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-2238T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665404 | ||||||
| chr1:99665461
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.127-2181T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665461 | ||||||
| chr1:99665484
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(46): Show | 50 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.127-2158G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665484 | ||||||
| chr1:99665615
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-2027A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665615 | ||||||
| chr1:99665735
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1907G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665735 | ||||||
| chr1:99666006
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1636A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666006 | ||||||
| chr1:99666143
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1499T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666143 | ||||||
| chr1:99666149
|
T | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1493T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666149 | ||||||
| chr1:99666192
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1450T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666192 | ||||||
| chr1:99666243
|
GT | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0036others(41): Show | 45 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.127-1389delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 99666243 | |||||
| chr1:99666355
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.127-1287G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666355 | ||||||
| chr1:99666403
|
C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.127-1239C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666403 | ||||||
| chr1:99666706
|
G | C | 2 | a0001c0001t0001g0141a0011c0015t0001g0139 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.127-936G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666706 | ||||||
| chr1:99666903
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-739G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666903 | ||||||
| chr1:99666991
|
C | T | 5 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-651C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666991 | ||||||
| chr1:99666992
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-650G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666992 | ||||||
| chr1:99667036
|
G | A | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-606G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667036 | ||||||
| chr1:99667365
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.127-277G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667365 | ||||||
| chr1:99667435
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.127-207G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667435 | ||||||
| chr1:99667445
|
G | A | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-197G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667445 | ||||||
| chr1:99667467
|
C | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-175C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667467 | ||||||
| chr1:99667521
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.127-121G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667521 | ||||||
| chr1:99667544
|
C | T | 3 | a0001c0001t0001g0295a0004c0006t0001g0309a0004c0006t0001g0310 | 3 | HG00735.hp1 HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.127-98C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667544 | ||||||
| chr1:99667598
|
T | C | 1 | a0001c0002t0002g0356 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-44T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667598 | ||||||
| chr1:99667620
|
T | C | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-22T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667620 | ||||||
| chr1:99667625
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-17A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667625 | ||||||
| chr1:99667882
|
CT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 88 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.251+130delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99667882 | |||||
| chr1:99667894
|
T | C | 1 | a0008c0013t0001g0344 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+128T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667894 | ||||||
| chr1:99667954
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.251+188C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667954 | ||||||
| chr1:99667976
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.251+210T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667976 | ||||||
| chr1:99668016
|
T | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0174 | 2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.251+250T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668016 | ||||||
| chr1:99668127
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.251+361G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668127 | ||||||
| chr1:99668155
|
G | A | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.251+389G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668155 | ||||||
| chr1:99668217
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0097 | 2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.251+451G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668217 | ||||||
| chr1:99668222
|
G | C | 1 | a0001c0001t0001g0008 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.251+456G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668222 | ||||||
| chr1:99668418
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(340): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.251+652A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668418 | ||||||
| chr1:99668449
|
T | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+683T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668449 | ||||||
| chr1:99668714
|
A | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.251+948A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668714 | ||||||
| chr1:99668717
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0215 | 3 | HG01123.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.251+951C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668717 | ||||||
| chr1:99668777
|
T | C | 9 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(6): Show | 9 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+1011T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668777 | ||||||
| chr1:99668847
|
A | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG00639.hp2 HG01261.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.251+1081A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668847 | ||||||
| chr1:99668997
|
A | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1231A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668997 | ||||||
| chr1:99669122
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1356G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669122 | ||||||
| chr1:99669183
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1417A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669183 | ||||||
| chr1:99669213
|
AACTG | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1452_251+1455d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99669213 | |||||
| chr1:99669341
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.251+1575G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669341 | ||||||
| chr1:99669636
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1870G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669636 | ||||||
| chr1:99669683
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1917G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669683 | ||||||
| chr1:99669738
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0235others(9): Show | 12 | HG00673.hp1 HG01070.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.251+1972C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669738 | ||||||
| chr1:99669752
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0140 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.251+1986C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669752 | ||||||
| chr1:99669780
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.251+2014G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669780 | ||||||
| chr1:99669781
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.251+2015G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669781 | ||||||
| chr1:99669786
|
G | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG02129.hp1 HG02135.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+2020G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669786 | ||||||
| chr1:99669845
|
A | G | 15 | a0001c0001t0001g0160a0001c0001t0001g0237a0001c0001t0006g0157others(12): Show | 15 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+2079A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669845 | ||||||
| chr1:99669850
|
G | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2084G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669850 | ||||||
| chr1:99669863
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+2097A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669863 | ||||||
| chr1:99669922
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251+2156G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669922 | ||||||
| chr1:99670099
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.251+2333T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670099 | ||||||
| chr1:99670107
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2341T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670107 | ||||||
| chr1:99670274
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | NA18970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.251+2508G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670274 | ||||||
| chr1:99670354
|
C | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2588C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670354 | ||||||
| chr1:99670361
|
C | T | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.251+2595C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670361 | ||||||
| chr1:99670382
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2616C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670382 | ||||||
| chr1:99670473
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.251+2707C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670473 | ||||||
| chr1:99670559
|
C | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2793C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670559 | ||||||
| chr1:99670773
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.251+3007T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670773 | ||||||
| chr1:99670887
|
T | TA | 11 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0167others(8): Show | 11 | HG02257.hp1 HG02683.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.251+3129dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99670887 | |||||
| chr1:99670987
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3221T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670987 | ||||||
| chr1:99671072
|
C | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(46): Show | 50 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.251+3306C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671072 | ||||||
| chr1:99671228
|
C | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0141a0011c0015t0001g0139 | 4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+3462C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671228 | ||||||
| chr1:99671232
|
G | A | 1 | a0001c0002t0001g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.251+3466G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671232 | ||||||
| chr1:99671276
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3510C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671276 | ||||||
| chr1:99671311
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3545T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671311 | ||||||
| chr1:99671315
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3549G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671315 | ||||||
| chr1:99671352
|
A | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3586A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671352 | ||||||
| chr1:99671364
|
T | G | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.251+3598T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671364 | ||||||
| chr1:99671425
|
AG | A | 6 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+3660delG | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671425 | ||||||
| chr1:99671551
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0202a0001c0001t0001g0217others(2): Show | 5 | HG00323.hp1 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+3785G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671551 | ||||||
| chr1:99671637
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3871A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671637 | ||||||
| chr1:99671691
|
T | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3925T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671691 | ||||||
| chr1:99671702
|
A | G | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.251+3936A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671702 | ||||||
| chr1:99671772
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02027.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.251+4006A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671772 | ||||||
| chr1:99671934
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4168A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671934 | ||||||
| chr1:99671947
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4181T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671947 | ||||||
| chr1:99672002
|
T | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0276 | 2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.251+4236T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672002 | ||||||
| chr1:99672036
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0036others(39): Show | 43 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.251+4270T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672036 | ||||||
| chr1:99672236
|
A | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4470A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672236 | ||||||
| chr1:99672251
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.251+4485G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672251 | ||||||
| chr1:99672310
|
T | C | 3 | a0003c0004t0001g0002a0003c0004t0001g0241a0003c0004t0005g0242 | 5 | HG02622.hp2 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+4544T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672310 | ||||||
| chr1:99672318
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4552G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672318 | ||||||
| chr1:99672337
|
T | C | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+4571T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672337 | ||||||
| chr1:99672379
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0112 | 2 | HG00609.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.251+4613G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672379 | ||||||
| chr1:99672399
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.251+4633C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672399 | ||||||
| chr1:99672485
|
T | C | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+4719T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672485 | ||||||
| chr1:99672508
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.251+4742T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672508 | ||||||
| chr1:99672554
|
T | A | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+4788T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672554 | ||||||
| chr1:99672656
|
T | C | 6 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+4890T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672656 | ||||||
| chr1:99672718
|
A | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4952A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672718 | ||||||
| chr1:99672734
|
C | T | 2 | a0004c0006t0001g0309a0004c0006t0001g0310 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.251+4968C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672734 | ||||||
| chr1:99672735
|
G | A | 1 | a0001c0012t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251+4969G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672735 | ||||||
| chr1:99672773
|
C | T | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5007C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672773 | ||||||
| chr1:99672781
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5015G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672781 | ||||||
| chr1:99672794
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.251+5028C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672794 | ||||||
| chr1:99672944
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.251+5178G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672944 | ||||||
| chr1:99672967
|
G | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5201G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672967 | ||||||
| chr1:99673036
|
T | C | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5270T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673036 | ||||||
| chr1:99673103
|
G | A | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5337G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673103 | ||||||
| chr1:99673244
|
T | C | 2 | a0001c0002t0002g0232a0001c0002t0002g0355 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.251+5478T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673244 | ||||||
| chr1:99673261
|
T | G | 4 | a0001c0001t0001g0361a0001c0002t0001g0300a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5495T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673261 | ||||||
| chr1:99673271
|
AT | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG00741.hp1 HG01106.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+5508delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99673271 | |||||
| chr1:99673480
|
G | GA | 5 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+5723dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99673480 | |||||
| chr1:99673515
|
G | T | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+5749G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673515 | ||||||
| chr1:99673586
|
T | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.251+5820T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673586 | ||||||
| chr1:99673587
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.251+5821C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673587 | ||||||
| chr1:99673588
|
G | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.251+5822G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673588 | ||||||
| chr1:99673702
|
A | G | 3 | a0001c0005t0001g0302a0001c0005t0001g0303a0001c0005t0001g0304 | 3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.251+5936A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673702 | ||||||
| chr1:99673716
|
C | T | 6 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+5950C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673716 | ||||||
| chr1:99673735
|
C | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.251+5969C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673735 | ||||||
| chr1:99673768
|
C | T | 1 | a0001c0001t0001g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.251+6002C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673768 | ||||||
| chr1:99673918
|
C | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6152C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673918 | ||||||
| chr1:99674065
|
C | A | 7 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(4): Show | 7 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+6299C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674065 | ||||||
| chr1:99674076
|
T | G | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6310T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674076 | ||||||
| chr1:99674174
|
C | T | 41 | a0001c0001t0001g0021a0001c0001t0001g0063a0001c0001t0001g0073others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.251+6408C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674174 | ||||||
| chr1:99674206
|
G | C | 1 | a0001c0001t0001g0368 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.251+6440G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674206 | ||||||
| chr1:99674299
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6533G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674299 | ||||||
| chr1:99674432
|
A | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+6666A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674432 | ||||||
| chr1:99674546
|
G | A | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+6780G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674546 | ||||||
| chr1:99674607
|
C | CA | 8 | a0001c0001t0001g0076a0001c0001t0001g0106a0001c0001t0001g0149others(5): Show | 8 | HG00741.hp2 HG01361.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.251+6855dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99674607 | |||||
| chr1:99674607
|
CA | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 23 | HG00544.hp1 HG01346.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.251+6855delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99674607 | |||||
| chr1:99674763
|
G | T | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+6997G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674763 | ||||||
| chr1:99674858
|
T | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(57): Show | 62 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.251+7092T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674858 | ||||||
| chr1:99674920
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.251+7154C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674920 | ||||||
| chr1:99674922
|
T | C | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7156T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674922 | ||||||
| chr1:99674931
|
G | C | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7165G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674931 | ||||||
| chr1:99674953
|
G | A | 14 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(11): Show | 14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+7187G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674953 | ||||||
| chr1:99674999
|
C | T | 11 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(8): Show | 11 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.251+7233C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674999 | ||||||
| chr1:99675000
|
G | A | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+7234G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675000 | ||||||
| chr1:99675002
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251+7236T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675002 | ||||||
| chr1:99675015
|
T | C | 1 | a0003c0004t0001g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.251+7249T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675015 | ||||||
| chr1:99675082
|
CTA | C | 14 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(11): Show | 14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+7318_251+7319d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99675082 | |||||
| chr1:99675194
|
A | G | 3 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0002t0001g0312 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7428A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675194 | ||||||
| chr1:99675213
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.251+7447T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675213 | ||||||
| chr1:99675221
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7455G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675221 | ||||||
| chr1:99675334
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.251+7568A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675334 | ||||||
| chr1:99675417
|
T | C | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7651T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675417 | ||||||
| chr1:99675527
|
C | T | 3 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0002t0001g0312 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675527 | ||||||
| chr1:99675568
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7802C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675568 | ||||||
| chr1:99675852
|
G | A | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+8086G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675852 | ||||||
| chr1:99675880
|
T | C | 3 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0002t0001g0312 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8114T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675880 | ||||||
| chr1:99675894
|
C | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8128C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675894 | ||||||
| chr1:99675901
|
T | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+8135T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675901 | ||||||
| chr1:99676002
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.251+8236G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676002 | ||||||
| chr1:99676057
|
T | G | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+8291T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676057 | ||||||
| chr1:99676321
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.251+8555A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676321 | ||||||
| chr1:99676332
|
T | C | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8566T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676332 | ||||||
| chr1:99676359
|
C | T | 5 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+8593C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676359 | ||||||
| chr1:99676387
|
G | A | 1 | a0008c0013t0001g0344 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+8621G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676387 | ||||||
| chr1:99676388
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0210 | 2 | NA18999.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.251+8622C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676388 | ||||||
| chr1:99676401
|
T | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8635T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676401 | ||||||
| chr1:99676414
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251+8648A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676414 | ||||||
| chr1:99676439
|
T | C | 5 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+8673T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676439 | ||||||
| chr1:99676627
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(53): Show | 58 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.251+8861G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676627 | ||||||
| chr1:99676639
|
G | A | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+8873G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676639 | ||||||
| chr1:99676782
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0147others(9): Show | 12 | HG00741.hp1 HG01081.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+9016G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676782 | ||||||
| chr1:99676783
|
TA | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(51): Show | 56 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.251+9024delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99676783 | |||||
| chr1:99676824
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.251+9058G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676824 | ||||||
| chr1:99676826
|
C | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+9060C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676826 | ||||||
| chr1:99676855
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+9089G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676855 | ||||||
| chr1:99676880
|
A | G | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9114A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676880 | ||||||
| chr1:99676925
|
A | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(50): Show | 55 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.251+9159A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676925 | ||||||
| chr1:99677030
|
G | C | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9264G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677030 | ||||||
| chr1:99677046
|
G | A | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9280G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677046 | ||||||
| chr1:99677092
|
G | T | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9326G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677092 | ||||||
| chr1:99677111
|
T | A | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9345T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677111 | ||||||
| chr1:99677235
|
T | TC | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9440dupC | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677235 | |||||
| chr1:99677248
|
G | GA | 12 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0078others(9): Show | 12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-9421dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677248 | |||||
| chr1:99677248
|
GA | G | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9421delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677248 | |||||
| chr1:99677443
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.252-9233C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677443 | ||||||
| chr1:99677484
|
C | T | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9192C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677484 | ||||||
| chr1:99677506
|
A | G | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9170A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677506 | ||||||
| chr1:99677607
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(365): Show | 378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.252-9069T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677607 | ||||||
| chr1:99677693
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.252-8983G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677693 | ||||||
| chr1:99677701
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-8975G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677701 | ||||||
| chr1:99677707
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0078others(9): Show | 12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-8969T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677707 | ||||||
| chr1:99677734
|
C | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0078others(9): Show | 12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-8942C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677734 | ||||||
| chr1:99677836
|
G | A | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-8840G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677836 | ||||||
| chr1:99677841
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.252-8835T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677841 | ||||||
| chr1:99677891
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0266a0001c0001t0001g0269others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-8785C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677891 | ||||||
| chr1:99677902
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.252-8774A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677902 | ||||||
| chr1:99678047
|
G | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.252-8629G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678047 | ||||||
| chr1:99678097
|
T | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.252-8579T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678097 | ||||||
| chr1:99678112
|
A | AT | 10 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0052others(7): Show | 11 | HG01074.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.252-8548dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678112 | |||||
| chr1:99678112
|
AT | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0138a0001c0001t0001g0189others(16): Show | 19 | HG00735.hp1 HG01070.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252-8548delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678112 | |||||
| chr1:99678116
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.252-8560T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678116 | ||||||
| chr1:99678228
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0209 | 2 | HG02080.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.252-8448C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678228 | ||||||
| chr1:99678236
|
G | A | 7 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(4): Show | 7 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-8440G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678236 | ||||||
| chr1:99678237
|
G | A | 14 | a0001c0001t0001g0237a0001c0002t0002g0231a0001c0002t0002g0232others(11): Show | 14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.252-8439G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678237 | ||||||
| chr1:99678240
|
TTA | T | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-8431_252-8430d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678240 | |||||
| chr1:99678266
|
A | C | 3 | a0001c0001t0004g0158a0001c0001t0004g0159a0008c0013t0001g0344 | 3 | HG02055.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-8410A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678266 | ||||||
| chr1:99678314
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.252-8362G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678314 | ||||||
| chr1:99678454
|
G | A | 2 | a0005c0009t0001g0011a0005c0009t0001g0012 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.252-8222G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678454 | ||||||
| chr1:99678491
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8185A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678491 | ||||||
| chr1:99678492
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8184C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678492 | ||||||
| chr1:99678493
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8183A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678493 | ||||||
| chr1:99678565
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.252-8111G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678565 | ||||||
| chr1:99678597
|
T | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-8079T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678597 | ||||||
| chr1:99678665
|
C | CA | 7 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(4): Show | 7 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-8007dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678665 | |||||
| chr1:99678670
|
T | C | 1 | a0001c0001t0001g0349 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.252-8006T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678670 | ||||||
| chr1:99678807
|
C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.252-7869C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678807 | ||||||
| chr1:99678966
|
T | TA | 15 | a0001c0001t0001g0120a0001c0001t0001g0290a0001c0001t0001g0348others(12): Show | 15 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-7695dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678966 | |||||
| chr1:99678966
|
TA | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(52): Show | 57 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.252-7695delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678966 | |||||
| chr1:99679042
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.252-7634G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679042 | ||||||
| chr1:99679171
|
C | T | 20 | a0001c0001t0001g0021a0001c0001t0001g0237a0001c0001t0001g0348others(17): Show | 20 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.252-7505C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679171 | ||||||
| chr1:99679412
|
G | T | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0002t0001g0357others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-7264G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679412 | ||||||
| chr1:99679472
|
C | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.252-7204C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679472 | ||||||
| chr1:99679532
|
A | C | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-7144A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679532 | ||||||
| chr1:99679533
|
A | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-7143A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679533 | ||||||
| chr1:99679623
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0339a0001c0001t0001g0340 | 3 | HG02602.hp1 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.252-7053T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679623 | ||||||
| chr1:99679887
|
A | G | 73 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(70): Show | 75 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.252-6789A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679887 | ||||||
| chr1:99679915
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0118a0001c0001t0001g0266others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.252-6761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679915 | ||||||
| chr1:99679947
|
A | G | 19 | a0001c0001t0001g0237a0001c0001t0001g0348a0001c0002t0001g0300others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-6729A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679947 | ||||||
| chr1:99680179
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.252-6497T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680179 | ||||||
| chr1:99680355
|
T | C | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-6321T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680355 | ||||||
| chr1:99680356
|
G | A | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-6320G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680356 | ||||||
| chr1:99680614
|
T | A | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-6062T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680614 | ||||||
| chr1:99680705
|
C | G | 1 | a0002c0003t0001g0352 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252-5971C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680705 | ||||||
| chr1:99680826
|
A | G | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-5850A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680826 | ||||||
| chr1:99680842
|
A | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5834A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680842 | ||||||
| chr1:99680851
|
C | CAT | 18 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0100others(15): Show | 18 | HG00140.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5812_252-5811d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99680851 | |||||
| chr1:99680861
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-5815T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680861 | ||||||
| chr1:99680875
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(69): Show | 74 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.252-5801G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680875 | ||||||
| chr1:99680915
|
C | T | 10 | a0001c0002t0002g0231a0001c0002t0002g0232a0001c0002t0002g0233others(7): Show | 10 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-5761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680915 | ||||||
| chr1:99681022
|
G | C | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5654G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681022 | ||||||
| chr1:99681097
|
G | T | 5 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(2): Show | 5 | HG01081.hp2 HG01192.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-5579G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681097 | ||||||
| chr1:99681101
|
A | G | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5575A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681101 | ||||||
| chr1:99681103
|
A | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5573A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681103 | ||||||
| chr1:99681105
|
A | ATG | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG01081.hp2 HG01192.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-5541_252-5540d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | |||||
| chr1:99681105
|
A | G | 2 | a0001c0001t0001g0348a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5571A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681105 | ||||||
| chr1:99681105
|
ATG | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(232): Show | 243 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.252-5541_252-5540d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | |||||
| chr1:99681105
|
ATGTG | A | 22 | a0001c0001t0001g0131a0001c0001t0001g0277a0001c0001t0001g0327others(19): Show | 22 | HG00544.hp1 HG00735.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.252-5543_252-5540d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | |||||
| chr1:99681105
|
ATGTGTG | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0135others(25): Show | 29 | HG00738.hp1 HG01167.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.252-5545_252-5540d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | |||||
| chr1:99681107
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0160others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-5569G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681107 | ||||||
| chr1:99681109
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.252-5567G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681109 | ||||||
| chr1:99681111
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0277a0001c0001t0001g0327 | 3 | HG01175.hp1 HG03453.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.252-5565G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681111 | ||||||
| chr1:99681127
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.252-5545_252-5536d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681127 | |||||
| chr1:99681129
|
G | A | 16 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5547G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681129 | ||||||
| chr1:99681131
|
GTGTGTA | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(38): Show | 42 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.252-5541_252-5536d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681131 | |||||
| chr1:99681133
|
G | A | 16 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5543G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681133 | ||||||
| chr1:99681135
|
G | A | 17 | a0001c0001t0002g0343a0001c0002t0001g0300a0001c0002t0001g0313others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5541G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681135 | ||||||
| chr1:99681135
|
GTATGTA | G | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(5): Show | 8 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-5537_252-5532d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681135 | |||||
| chr1:99681137
|
A | G | 2 | a0001c0001t0002g0343a0001c0002t0001g0312 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.252-5539A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681137 | ||||||
| chr1:99681139
|
G | A | 17 | a0001c0001t0002g0343a0001c0002t0001g0300a0001c0002t0001g0313others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5537G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681139 | ||||||
| chr1:99681142
|
T | G | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5534T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681142 | ||||||
| chr1:99681143
|
A | G | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5533A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681143 | ||||||
| chr1:99681144
|
T | G | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5532T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681144 | ||||||
| chr1:99681146
|
T | G | 12 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(9): Show | 12 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-5530T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681146 | ||||||
| chr1:99681148
|
T | G | 16 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5528T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681148 | ||||||
| chr1:99681150
|
T | G | 16 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5526T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681150 | ||||||
| chr1:99681152
|
T | G | 16 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5524T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681152 | ||||||
| chr1:99681153
|
G | A | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5523G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681153 | ||||||
| chr1:99681154
|
T | G | 17 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0313others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5522T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681154 | ||||||
| chr1:99681156
|
T | G | 17 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0313others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5520T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681156 | ||||||
| chr1:99681156
|
T | TAGAGAGA others(5): Show |
1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5516_252-5515i others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681156 | |||||
| chr1:99681220
|
A | G | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5456A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681220 | ||||||
| chr1:99681228
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.252-5448A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681228 | ||||||
| chr1:99681248
|
T | A | 6 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(3): Show | 6 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-5428T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681248 | ||||||
| chr1:99681287
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.252-5389G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681287 | ||||||
| chr1:99681384
|
C | T | 1 | a0004c0006t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5292C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681384 | ||||||
| chr1:99681605
|
G | A | 1 | a0002c0003t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-5071G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681605 | ||||||
| chr1:99681731
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.252-4945A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681731 | ||||||
| chr1:99681780
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252-4896G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681780 | ||||||
| chr1:99681834
|
A | G | 73 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0037others(70): Show | 75 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.252-4842A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681834 | ||||||
| chr1:99681835
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.252-4841C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681835 | ||||||
| chr1:99681865
|
C | G | 17 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-4811C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681865 | ||||||
| chr1:99681964
|
C | G | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-4712C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681964 | ||||||
| chr1:99681967
|
G | C | 18 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-4709G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681967 | ||||||
| chr1:99682010
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.252-4666T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682010 | ||||||
| chr1:99682027
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252-4649G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682027 | ||||||
| chr1:99682031
|
G | A | 10 | a0001c0001t0001g0348a0002c0003t0001g0081a0002c0003t0001g0229others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-4645G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682031 | ||||||
| chr1:99682053
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.252-4623G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682053 | ||||||
| chr1:99682425
|
C | T | 27 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(24): Show | 27 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.252-4251C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682425 | ||||||
| chr1:99682431
|
C | T | 27 | a0001c0001t0001g0348a0001c0002t0001g0300a0001c0002t0001g0312others(24): Show | 27 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.252-4245C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682431 | ||||||
| chr1:99682444
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-4232C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682444 | ||||||
| chr1:99682539
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-4137T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682539 | ||||||
| chr1:99682585
|
C | T | 1 | a0001c0001t0001g0348 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-4091C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682585 | ||||||
| chr1:99682647
|
G | A | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-4029G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682647 | ||||||
| chr1:99682723
|
A | G | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3953A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682723 | ||||||
| chr1:99682735
|
C | T | 4 | a0001c0005t0001g0296a0001c0005t0001g0302a0001c0005t0001g0303others(1): Show | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3941C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682735 | ||||||
| chr1:99682736
|
G | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-3940G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682736 | ||||||
| chr1:99682742
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.252-3934A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682742 | ||||||
| chr1:99682817
|
T | C | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3859T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682817 | ||||||
| chr1:99682824
|
G | A | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3852G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682824 | ||||||
| chr1:99682942
|
G | T | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3734G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682942 | ||||||
| chr1:99682945
|
A | G | 33 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(30): Show | 33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3731A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682945 | ||||||
| chr1:99682948
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.252-3728G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682948 | ||||||
| chr1:99682955
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.252-3721G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682955 | ||||||
| chr1:99683003
|
CTCCAAAA others(1): Show |
C | 9 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(6): Show | 9 | HG00544.hp1 HG01346.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.252-3672_252-3665d others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | ||||||
| chr1:99683003
|
CTCCAAAA others(13): Show |
C | 1 | a0002c0003t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-3672_252-3653d others(22): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | ||||||
| chr1:99683003
|
CTCCAAAA others(17): Show |
C | 3 | a0001c0002t0001g0300a0001c0002t0001g0313a0001c0002t0001g0362 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-3672_252-3649d others(26): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | ||||||
| chr1:99683003
|
CTCCAAAA others(21): Show |
C | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-3672_252-3645d others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | ||||||
| chr1:99683003
|
CTCCAAAA others(79): Show |
C | 9 | a0002c0003t0001g0229a0002c0003t0001g0352a0002c0003t0001g0353others(6): Show | 11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3672_252-3587d others(88): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | ||||||
| chr1:99683004
|
T | G | 11 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(8): Show | 11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3672T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683004 | ||||||
| chr1:99683005
|
C | A | 11 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(8): Show | 11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3671C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683005 | ||||||
| chr1:99683006
|
C | A | 11 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(8): Show | 11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3670C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683006 | ||||||
| chr1:99683008
|
A | G | 13 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3668A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683008 | ||||||
| chr1:99683019
|
G | A | 22 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(19): Show | 22 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.252-3657G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683019 | ||||||
| chr1:99683019
|
G | GGAAA | 3 | a0001c0001t0001g0092a0001c0001t0001g0106a0001c0001t0001g0113 | 3 | HG02056.hp2 HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.252-3622_252-3619d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | |||||
| chr1:99683019
|
G | GGAAAGAA others(5): Show |
1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.252-3630_252-3619d others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | |||||
| chr1:99683019
|
GGA | G | 3 | a0001c0001t0001g0172a0001c0001t0001g0266a0001c0001t0001g0322 | 3 | HG02735.hp1 HG03540.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.252-3656_252-3655d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683019 | ||||||
| chr1:99683019
|
GGAAAGAA others(63): Show |
G | 16 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-3618_252-3549d others(72): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | |||||
| chr1:99683019
|
GGAAAGAA others(67): Show |
G | 5 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0059others(2): Show | 5 | HG01361.hp1 HG01928.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3618_252-3545d others(76): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | |||||
| chr1:99683019
|
GGAAAGAA others(71): Show |
G | 5 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0058others(2): Show | 5 | HG00280.hp2 HG00438.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3618_252-3541d others(80): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | |||||
| chr1:99683021
|
AAAGAAAG others(56): Show |
A | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.252-3653_252-3591d others(65): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683021 | |||||
| chr1:99683022
|
AAGAAAGA others(59): Show |
A | 19 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0066others(16): Show | 19 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-3618_252-3553d others(68): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683022 | |||||
| chr1:99683023
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(17): Show | 21 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.252-3653A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683023 | ||||||
| chr1:99683026
|
AAGAAAGA others(55): Show |
A | 22 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(19): Show | 22 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.252-3618_252-3557d others(64): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683026 | |||||
| chr1:99683029
|
AAAGAAAG others(66): Show |
A | 1 | a0001c0001t0001g0351 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252-3644_252-3572d others(75): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683029 | |||||
| chr1:99683030
|
AAGAAAGA others(51): Show |
A | 28 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(25): Show | 30 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.252-3618_252-3561d others(60): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683030 | |||||
| chr1:99683033
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-3643A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683033 | ||||||
| chr1:99683034
|
AAGAAAGA others(47): Show |
A | 40 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(37): Show | 41 | HG00408.hp1 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.252-3618_252-3565d others(56): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683034 | |||||
| chr1:99683038
|
AAGAAAGA others(43): Show |
A | 37 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0016others(34): Show | 39 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.252-3618_252-3569d others(52): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683038 | |||||
| chr1:99683040
|
GAAAGAAA others(44): Show |
G | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-3633_252-3583d others(53): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683040 | |||||
| chr1:99683042
|
AAGAAAGA others(39): Show |
A | 21 | a0001c0001t0001g0023a0001c0001t0001g0118a0001c0001t0001g0131others(18): Show | 21 | HG00621.hp1 HG01070.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.252-3618_252-3573d others(48): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683042 | |||||
| chr1:99683046
|
AAGAAAGA others(3): Show |
A | 2 | a0001c0001t0001g0028a0001c0001t0001g0091 | 2 | NA18954.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.252-3626_252-3617d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683046 | |||||
| chr1:99683046
|
AAGAAAGA others(35): Show |
A | 16 | a0001c0001t0001g0133a0001c0001t0001g0148a0001c0001t0001g0167others(13): Show | 16 | HG00140.hp2 HG00597.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.252-3618_252-3577d others(44): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683046 | |||||
| chr1:99683048
|
GAAAGAA | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0144 | 3 | HG02135.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.252-3626_252-3621d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683048 | |||||
| chr1:99683050
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.252-3626A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683050 | ||||||
| chr1:99683050
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0289 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.252-3622_252-3613d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683050 | |||||
| chr1:99683050
|
AAGAAAGA others(31): Show |
A | 5 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0076others(2): Show | 7 | HG00673.hp2 HG03098.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-3618_252-3581d others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683050 | |||||
| chr1:99683053
|
AAAG | A | 3 | a0001c0001t0001g0324a0001c0001t0001g0337a0006c0007t0001g0329 | 3 | HG01258.hp1 HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.252-3621_252-3619d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683053 | |||||
| chr1:99683054
|
A | AAGAAGAG others(6): Show |
1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.252-3619_252-3618i others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | |||||
| chr1:99683054
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0082others(10): Show | 14 | HG00323.hp2 HG00738.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.252-3622A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683054 | ||||||
| chr1:99683054
|
AAGAGAGA others(15): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.252-3606_252-3585d others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | |||||
| chr1:99683054
|
AAGAGAGA others(19): Show |
A | 1 | a0001c0001t0001g0073 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.252-3610_252-3585d others(28): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | |||||
| chr1:99683054
|
AAGAGAGA others(23): Show |
A | 2 | a0001c0001t0001g0127a0001c0001t0001g0129 | 2 | NA18978.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.252-3614_252-3585d others(32): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | |||||
| chr1:99683054
|
AAGAGAGA others(27): Show |
A | 12 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0216others(9): Show | 12 | HG00673.hp1 HG02165.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-3618_252-3585d others(36): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | |||||
| chr1:99683056
|
G | GAAAGAAA others(3): Show |
2 | a0001c0001t0001g0339a0001c0005t0001g0304 | 2 | HG02698.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.252-3619_252-3618i others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | |||||
| chr1:99683056
|
G | GAAAGAAA others(7): Show |
1 | a0001c0005t0001g0303 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252-3619_252-3618i others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | |||||
| chr1:99683056
|
G | GAAAGAAA others(11): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0290 | 2 | HG02602.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.252-3619_252-3618i others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | |||||
| chr1:99683056
|
G | GAAAGAAA others(19): Show |
1 | a0001c0005t0001g0296 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252-3619_252-3618i others(28): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | |||||
| chr1:99683058
|
G | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0033others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.252-3618G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683058 | ||||||
| chr1:99683060
|
G | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0339a0001c0005t0001g0296others(3): Show | 6 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3616G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683060 | ||||||
| chr1:99683062
|
G | A | 34 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0083others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.252-3614G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683062 | ||||||
| chr1:99683064
|
G | A | 6 | a0001c0001t0001g0290a0001c0001t0001g0339a0001c0005t0001g0296others(3): Show | 6 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3612G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683064 | ||||||
| chr1:99683065
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0107 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.252-3611_252-3610i others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683065 | ||||||
| chr1:99683066
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0106others(11): Show | 14 | HG00544.hp2 HG00609.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.252-3610G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683066 | ||||||
| chr1:99683068
|
G | A | 5 | a0001c0001t0001g0290a0001c0005t0001g0296a0001c0005t0001g0302others(2): Show | 5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3608G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683068 | ||||||
| chr1:99683070
|
G | A | 3 | a0001c0001t0001g0146a0001c0002t0002g0356a0005c0009t0001g0011 | 3 | HG03927.hp2 NA18960.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3606G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683070 | ||||||
| chr1:99683072
|
G | A | 5 | a0001c0001t0001g0290a0001c0005t0001g0296a0001c0005t0001g0302others(2): Show | 5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3604G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683072 | ||||||
| chr1:99683074
|
G | A | 1 | a0005c0009t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.252-3602G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683074 | ||||||
| chr1:99683074
|
GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.252-3598_252-3577d others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683074 | |||||
| chr1:99683074
|
GAGAGAGA others(55): Show |
G | 1 | a0002c0003t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-3598_252-3537d others(64): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683074 | |||||
| chr1:99683076
|
G | A | 5 | a0001c0001t0001g0290a0001c0005t0001g0296a0001c0005t0001g0302others(2): Show | 5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3600G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683076 | ||||||
| chr1:99683076
|
GAGAGAGA others(25): Show |
G | 1 | a0001c0001t0001g0082 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.252-3596_252-3565d others(34): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683076 | |||||
| chr1:99683078
|
GAGAGAGA others(31): Show |
G | 1 | a0001c0001t0001g0365 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252-3594_252-3557d others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683078 | |||||
| chr1:99683078
|
GAGAGAGA others(51): Show |
G | 1 | a0001c0002t0001g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.252-3594_252-3537d others(60): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683078 | |||||
| chr1:99683080
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0290a0001c0005t0001g0296others(3): Show | 6 | HG02451.hp2 HG02683.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3596G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683080 | ||||||
| chr1:99683080
|
GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0001g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.252-3592_252-3573d others(22): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683080 | |||||
| chr1:99683080
|
GAGAGAGA others(49): Show |
G | 2 | a0001c0002t0001g0313a0001c0002t0001g0362 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-3592_252-3537d others(58): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683080 | |||||
| chr1:99683082
|
GAGAGAGA others(7): Show |
G | 2 | a0001c0001t0001g0004a0001c0001t0001g0143 | 3 | HG01934.hp1 NA19055.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.252-3590_252-3577d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | |||||
| chr1:99683082
|
GAGAGAGA others(11): Show |
G | 1 | a0001c0001t0001g0126 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.252-3590_252-3573d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | |||||
| chr1:99683082
|
GAGAGAGA others(47): Show |
G | 1 | a0001c0002t0001g0312 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-3590_252-3537d others(56): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | |||||
| chr1:99683084
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0290others(4): Show | 7 | HG02451.hp2 HG02683.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-3592G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683084 | ||||||
| chr1:99683084
|
GAGAGAGA others(8): Show |
G | 1 | a0001c0001t0001g0097 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.252-3590_252-3576d others(17): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683084 | |||||
| chr1:99683084
|
GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0001g0099a0001c0001t0001g0161a0001c0001t0001g0332 | 3 | HG00323.hp2 HG02300.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.252-3588_252-3573d others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683084 | |||||
| chr1:99683086
|
GAGAGAAA others(3): Show |
G | 2 | a0001c0001t0001g0078a0001c0001t0001g0345 | 2 | HG01069.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.252-3586_252-3577d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | |||||
| chr1:99683086
|
GAGAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.252-3588_252-3576d others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | |||||
| chr1:99683086
|
GAGAGAAA others(7): Show |
G | 2 | a0001c0001t0001g0330a0001c0001t0001g0367 | 2 | HG00280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.252-3586_252-3573d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | |||||
| chr1:99683086
|
GAGAGAAA others(11): Show |
G | 1 | a0001c0001t0001g0336 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.252-3586_252-3569d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | |||||
| chr1:99683086
|
GAGAGAAA others(30): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.252-3588_252-3552d others(39): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | |||||
| chr1:99683088
|
G | A | 10 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0127others(7): Show | 10 | HG01943.hp2 HG02451.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-3588G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683088 | ||||||
| chr1:99683088
|
GAGAA | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0102a0001c0001t0001g0287others(2): Show | 5 | HG01167.hp1 HG02015.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3510_252-3507d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | |||||
| chr1:99683088
|
GAGAAAGA others(1): Show |
G | 8 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0103others(5): Show | 8 | HG00408.hp2 HG01934.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-3514_252-3507d others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | |||||
| chr1:99683088
|
GAGAAAGA others(5): Show |
G | 5 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0090others(2): Show | 5 | HG00738.hp1 HG01975.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3518_252-3507d others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | |||||
| chr1:99683088
|
GAGAAAGA others(9): Show |
G | 2 | a0001c0001t0001g0104a0001c0001t0001g0326 | 2 | HG00639.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.252-3522_252-3507d others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | |||||
| chr1:99683089
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0138a0001c0001t0001g0249 | 3 | HG04184.hp1 NA19058.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.252-3587A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683089 | ||||||
| chr1:99683090
|
GAA | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0112others(3): Show | 6 | HG00423.hp1 HG00609.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-3584_252-3583d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683090
|
GAAAGAA | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0080others(6): Show | 9 | HG01081.hp2 HG01175.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.252-3584_252-3579d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683090
|
GAAAGAAA others(3): Show |
G | 15 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(12): Show | 15 | HG01978.hp1 HG01981.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.252-3584_252-3575d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683090
|
GAAAGAAA others(7): Show |
G | 2 | a0001c0001t0001g0083a0001c0001t0001g0088 | 2 | HG02738.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.252-3584_252-3571d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683090
|
GAAAGAAA others(11): Show |
G | 3 | a0001c0001t0001g0100a0001c0001t0001g0315a0006c0007t0001g0329 | 3 | HG01258.hp1 HG01361.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.252-3584_252-3567d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683090
|
GAAAGAAA others(14): Show |
G | 1 | a0006c0007t0001g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.252-3583_252-3563d others(23): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | |||||
| chr1:99683091
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0001g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.252-3582_252-3572d others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683091 | |||||
| chr1:99683092
|
A | G | 40 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0035others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.252-3584A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683092 | ||||||
| chr1:99683093
|
A | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00639.hp2 HG01261.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-3583A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683093 | ||||||
| chr1:99683096
|
A | G | 42 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0091others(39): Show | 42 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.252-3580A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683096 | ||||||
| chr1:99683097
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0059 | 3 | HG01928.hp2 NA18986.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252-3579A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683097 | ||||||
| chr1:99683099
|
A | G | 2 | a0001c0001t0001g0346a0001c0001t0003g0239 | 2 | HG01169.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.252-3577A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683099 | ||||||
| chr1:99683100
|
A | G | 44 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0080others(41): Show | 44 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-3576A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683100 | ||||||
| chr1:99683101
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0058others(1): Show | 4 | HG00280.hp2 HG00438.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3575A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683101 | ||||||
| chr1:99683103
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.252-3573A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683103 | ||||||
| chr1:99683103
|
AAAGAAAG others(40): Show |
A | 3 | a0001c0002t0001g0263a0001c0002t0002g0306a0005c0009t0001g0012 | 3 | HG01167.hp2 HG02723.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.252-3570_252-3524d others(49): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683103 | |||||
| chr1:99683104
|
A | AAG | 3 | a0001c0005t0001g0296a0001c0005t0001g0302a0001c0005t0001g0304 | 3 | HG02970.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.252-3570_252-3569d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683104 | |||||
| chr1:99683104
|
A | G | 33 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 33 | HG00408.hp2 HG01081.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3572A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683104 | ||||||
| chr1:99683107
|
AAAGAAAG others(36): Show |
A | 3 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0262 | 3 | HG00544.hp1 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.252-3566_252-3524d others(45): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683107 | |||||
| chr1:99683108
|
A | G | 11 | a0001c0001t0001g0111a0001c0001t0001g0287a0001c0001t0001g0335others(8): Show | 11 | HG01192.hp2 HG01346.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3568A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683108 | ||||||
| chr1:99683111
|
AAAGAAAG others(32): Show |
A | 5 | a0001c0002t0002g0280a0001c0002t0002g0369a0005c0009t0001g0011others(2): Show | 5 | HG01884.hp1 HG03471.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3562_252-3524d others(41): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683111 | |||||
| chr1:99683112
|
A | G | 6 | a0001c0001t0001g0100a0001c0002t0001g0024a0001c0002t0001g0357others(3): Show | 6 | HG01346.hp2 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-3564A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683112 | ||||||
| chr1:99683115
|
AAAGAAAG others(28): Show |
A | 4 | a0001c0002t0001g0261a0001c0002t0002g0234a0001c0002t0002g0305others(1): Show | 4 | HG03209.hp2 HG04199.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-3558_252-3524d others(37): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683115 | |||||
| chr1:99683116
|
A | G | 3 | a0001c0002t0001g0024a0001c0002t0001g0357a0001c0002t0002g0356 | 3 | HG01346.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3560A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683116 | ||||||
| chr1:99683119
|
AAAGAAAG others(24): Show |
A | 2 | a0001c0002t0002g0232a0001c0002t0002g0355 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.252-3554_252-3524d others(33): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683119 | |||||
| chr1:99683120
|
A | G | 11 | a0001c0002t0001g0357a0001c0002t0002g0356a0002c0003t0001g0229others(8): Show | 13 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3556A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683120 | ||||||
| chr1:99683123
|
AAAGAAAG others(20): Show |
A | 3 | a0001c0002t0001g0024a0001c0002t0002g0231a0001c0002t0002g0233 | 3 | HG01346.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.252-3550_252-3524d others(29): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683123 | |||||
| chr1:99683124
|
A | G | 11 | a0001c0002t0001g0357a0001c0002t0002g0356a0002c0003t0001g0229others(8): Show | 13 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3552A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683124 | ||||||
| chr1:99683128
|
A | G | 10 | a0001c0002t0002g0356a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-3548A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683128 | ||||||
| chr1:99683132
|
A | G | 9 | a0002c0003t0001g0229a0002c0003t0001g0352a0002c0003t0001g0353others(6): Show | 11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3544A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683132 | ||||||
| chr1:99683136
|
A | G | 9 | a0002c0003t0001g0229a0002c0003t0001g0352a0002c0003t0001g0353others(6): Show | 11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3540A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683136 | ||||||
| chr1:99683144
|
AAG | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | NA18948.hp2 NA18993.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.252-3530_252-3529d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683144 | |||||
| chr1:99683147
|
AAAG | A | 15 | a0001c0002t0001g0300a0001c0002t0001g0312a0001c0002t0001g0313others(12): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.252-3526_252-3524d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683147 | |||||
| chr1:99683161
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.252-3515A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683161 | ||||||
| chr1:99683162
|
GAAA | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(33): Show | 38 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3513_252-3511d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683162 | ||||||
| chr1:99683165
|
A | AG | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG00673.hp1 NA18970.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3510dupG | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683165 | |||||
| chr1:99683165
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.252-3511A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683165 | ||||||
| chr1:99683170
|
C | G | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.252-3506C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683170 | ||||||
| chr1:99683180
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.252-3496A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683180 | ||||||
| chr1:99683312
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.252-3364A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683312 | ||||||
| chr1:99683325
|
C | A | 1 | a0001c0001t0001g0348 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-3351C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683325 | ||||||
| chr1:99683327
|
G | C | 4 | a0001c0002t0001g0300a0001c0002t0001g0312a0001c0002t0001g0313others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3349G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683327 | ||||||
| chr1:99683453
|
A | AT | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3221dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683453 | |||||
| chr1:99683560
|
G | C | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3116G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683560 | ||||||
| chr1:99683621
|
A | G | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3055A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683621 | ||||||
| chr1:99683648
|
A | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0037others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.252-3028A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683648 | ||||||
| chr1:99683649
|
T | C | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3027T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683649 | ||||||
| chr1:99683752
|
G | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.252-2924G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683752 | ||||||
| chr1:99683899
|
G | A | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2777G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683899 | ||||||
| chr1:99683917
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.252-2759G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683917 | ||||||
| chr1:99683924
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.252-2752C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683924 | ||||||
| chr1:99683953
|
T | C | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.252-2723T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683953 | ||||||
| chr1:99684046
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0174 | 2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.252-2630A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684046 | ||||||
| chr1:99684077
|
T | G | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | HG00544.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.252-2599T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684077 | ||||||
| chr1:99684096
|
A | G | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2580A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684096 | ||||||
| chr1:99684103
|
T | C | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2573T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684103 | ||||||
| chr1:99684259
|
G | A | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2417G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684259 | ||||||
| chr1:99684275
|
A | G | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2401A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684275 | ||||||
| chr1:99684314
|
C | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2362C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684314 | ||||||
| chr1:99684331
|
G | A | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2345G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684331 | ||||||
| chr1:99684337
|
C | T | 37 | a0001c0001t0001g0009a0001c0001t0001g0348a0001c0002t0001g0014others(34): Show | 39 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.252-2339C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684337 | ||||||
| chr1:99684362
|
A | G | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2314A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684362 | ||||||
| chr1:99684396
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2280C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684396 | ||||||
| chr1:99684422
|
T | A | 1 | a0001c0001t0001g0348 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-2254T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684422 | ||||||
| chr1:99684466
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2210T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684466 | ||||||
| chr1:99684471
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.252-2205G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684471 | ||||||
| chr1:99684521
|
T | C | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2155T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684521 | ||||||
| chr1:99684541
|
T | TTTTG | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2135_252-2134i others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684541 | ||||||
| chr1:99684544
|
C | A | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2132C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684544 | ||||||
| chr1:99684565
|
C | T | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2111C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684565 | ||||||
| chr1:99684616
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.252-2060G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684616 | ||||||
| chr1:99684721
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0146 | 2 | HG01496.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.252-1955T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684721 | ||||||
| chr1:99684751
|
A | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0004g0158others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-1925A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684751 | ||||||
| chr1:99684804
|
C | T | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 5 | HG02257.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-1872C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684804 | ||||||
| chr1:99684943
|
A | C | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1733A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684943 | ||||||
| chr1:99684980
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.252-1696G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684980 | ||||||
| chr1:99685031
|
G | C | 13 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(10): Show | 13 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.252-1645G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685031 | ||||||
| chr1:99685166
|
ATCTG | A | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1504_252-1501d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99685166 | |||||
| chr1:99685268
|
A | G | 36 | a0001c0001t0001g0348a0001c0002t0001g0014a0001c0002t0001g0024others(33): Show | 38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1408A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685268 | ||||||
| chr1:99685336
|
T | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0004g0158others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-1340T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685336 | ||||||
| chr1:99685452
|
A | G | 13 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(10): Show | 13 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.252-1224A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685452 | ||||||
| chr1:99685481
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-1195A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685481 | ||||||
| chr1:99685532
|
G | A | 2 | a0004c0006t0001g0309a0004c0006t0001g0310 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.252-1144G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685532 | ||||||
| chr1:99685547
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-1129C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685547 | ||||||
| chr1:99685616
|
A | G | 2 | a0001c0002t0002g0232a0001c0002t0002g0355 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.252-1060A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685616 | ||||||
| chr1:99685660
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.252-1016A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685660 | ||||||
| chr1:99685841
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-835G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685841 | ||||||
| chr1:99685920
|
C | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-756C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685920 | ||||||
| chr1:99685928
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.252-748T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685928 | ||||||
| chr1:99686030
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-646A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686030 | ||||||
| chr1:99686034
|
C | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0004g0158others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-642C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686034 | ||||||
| chr1:99686135
|
C | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-541C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686135 | ||||||
| chr1:99686279
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0161 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.252-397G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686279 | ||||||
| chr1:99686400
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0174 | 2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.252-276C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686400 | ||||||
| chr1:99686422
|
G | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.252-254G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686422 | ||||||
| chr1:99686476
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(39): Show | 44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-200G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686476 | ||||||
| chr1:99686515
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-161A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686515 | ||||||
| chr1:99686524
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-152A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686524 | ||||||
| chr1:99686536
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-140A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686536 | ||||||
| chr1:99686549
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-127A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686549 | ||||||
| chr1:99686612
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0097 | 2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.252-64C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686612 | ||||||
| chr1:99686627
|
C | T | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-49C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686627 | ||||||
| chr1:99686650
|
T | C | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-26T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686650 | ||||||
| chr1:99686853
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.366+63A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686853 | ||||||
| chr1:99686887
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.367-43T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686887 | ||||||
| chr1:99686916
|
C | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0226 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.367-14C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686916 | ||||||
| chr1:99687020
|
T | C | 2 | a0004c0006t0001g0309a0004c0006t0001g0310 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-56T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 5/7 | chr1 | 99687020 | ||||||
| chr1:99687210
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.514+21G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687210 | ||||||
| chr1:99687243
|
G | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG01934.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.514+54G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687243 | ||||||
| chr1:99687349
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0137others(2): Show | 5 | HG00408.hp2 HG00609.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+160T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687349 | ||||||
| chr1:99687368
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.514+179T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687368 | ||||||
| chr1:99687431
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.514+242G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687431 | ||||||
| chr1:99687585
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.514+396A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687585 | ||||||
| chr1:99687649
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.514+460A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687649 | ||||||
| chr1:99687687
|
ACT | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(68): Show | 73 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.514+501_514+502del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99687687 | |||||
| chr1:99687707
|
A | G | 1 | a0001c0001t0008g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.514+518A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687707 | ||||||
| chr1:99687866
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.514+677C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687866 | ||||||
| chr1:99687897
|
G | GA | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.514+710dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99687897 | |||||
| chr1:99687935
|
G | A | 2 | a0001c0002t0002g0232a0001c0002t0002g0355 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.514+746G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687935 | ||||||
| chr1:99688060
|
T | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0170a0001c0001t0001g0176others(2): Show | 5 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.515-715T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688060 | ||||||
| chr1:99688118
|
C | T | 105 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(102): Show | 109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.515-657C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688118 | ||||||
| chr1:99688460
|
A | G | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.515-315A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688460 | ||||||
| chr1:99688469
|
CTT | C | 35 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(32): Show | 37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.515-302_515-301del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99688469 | |||||
| chr1:99688498
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0236 | 2 | HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.515-277C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688498 | ||||||
| chr1:99688499
|
T | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.515-276T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688499 | ||||||
| chr1:99688530
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.515-245C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688530 | ||||||
| chr1:99688561
|
CA | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0101others(2): Show | 6 | NA18999.hp1 NA19002.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-213delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688561 | ||||||
| chr1:99688573
|
C | A | 15 | a0001c0002t0001g0357a0001c0002t0002g0231a0001c0002t0002g0232others(12): Show | 15 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.515-202C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688573 | ||||||
| chr1:99688677
|
T | C | 21 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0261others(18): Show | 21 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.515-98T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688677 | ||||||
| chr1:99690253
|
T | G | 38 | a0001c0001t0002g0343a0001c0001t0004g0158a0001c0001t0004g0159others(35): Show | 40 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.1612+381T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690253 | ||||||
| chr1:99690292
|
A | C | 14 | a0001c0001t0002g0343a0001c0002t0001g0357a0001c0002t0002g0231others(11): Show | 14 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612+420A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690292 | ||||||
| chr1:99690345
|
T | G | 1 | a0001c0001t0001g0327 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1612+473T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690345 | ||||||
| chr1:99690421
|
AT | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(51): Show | 56 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1612+553delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 99690421 | |||||
| chr1:99690498
|
A | G | 22 | a0001c0001t0002g0343a0001c0002t0001g0014a0001c0002t0001g0024others(19): Show | 22 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1612+626A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690498 | ||||||
| chr1:99690517
|
T | C | 1 | a0001c0001t0006g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1612+645T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690517 | ||||||
| chr1:99690633
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 57 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1612+761A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690633 | ||||||
| chr1:99690702
|
G | A | 10 | a0002c0003t0001g0081a0002c0003t0001g0229a0002c0003t0001g0352others(7): Show | 12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1612+830G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690702 | ||||||
| chr1:99690772
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1612+900A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690772 | ||||||
| chr1:99690867
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1612+995A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690867 | ||||||
| chr1:99691102
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(250): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1612+1230T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691102 | ||||||
| chr1:99691145
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1612+1273G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691145 | ||||||
| chr1:99691160
|
A | G | 2 | a0001c0002t0001g0014a0007c0011t0001g0013 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1612+1288A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691160 | ||||||
| chr1:99691261
|
T | C | 6 | a0001c0001t0002g0343a0001c0002t0002g0280a0001c0002t0002g0305others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1612+1389T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691261 | ||||||
| chr1:99691640
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1612+1768A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691640 | ||||||
| chr1:99691767
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1612+1895A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691767 | ||||||
| chr1:99692160
|
A | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(7): Show | 10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1859A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692160 | ||||||
| chr1:99692326
|
C | A | 38 | a0001c0001t0002g0343a0001c0001t0004g0158a0001c0001t0004g0159others(35): Show | 40 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.1613-1693C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692326 | ||||||
| chr1:99692632
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(7): Show | 10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1387C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692632 | ||||||
| chr1:99692901
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(89): Show | 96 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1613-1118T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692901 | ||||||
| chr1:99692994
|
A | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(7): Show | 10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1025A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692994 | ||||||
| chr1:99693356
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1613-663C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693356 | ||||||
| chr1:99693473
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1613-546A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693473 | ||||||
| chr1:99693536
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1613-483G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693536 | ||||||
| chr1:99693744
|
T | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(79): Show | 86 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1613-275T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693744 | ||||||
| chr1:99693750
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1613-269C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693750 | ||||||
| chr1:99693828
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | NA18955.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1613-191C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693828 | ||||||
| chr1:99693833
|
T | G | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1613-186T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693833 | ||||||
| chr1:99693862
|
T | C | 66 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(63): Show | 68 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1613-157T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693862 | ||||||
| chr1:99693910
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1613-109A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693910 | ||||||
| chr1:99693981
|
T | G | 1 | a0008c0013t0001g0344 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1613-38T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693981 | ||||||
| chr1:99693996
|
C | CT | 76 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(73): Show | 78 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1613-14dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 99693996 |