Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 90826 |
|---|---|
| ensemblid | ENSG00000164169.13 |
| hgncid | 25099 |
| symbol | PRMT9 |
| name | protein arginine methyltransferase 9 |
| refseq_nuc | NM_138364.4 |
| refseq_prot | NP_612373.2 |
| ensembl_nuc | ENST00000322396.7 |
| ensembl_prot | ENSP00000314396.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 147637785 |
| end | 147684163 |
| strand | - |
| ver | v1.2 |
| region | chr4:147637785-147684163 |
| region5000 | chr4:147632785-147689163 |
| regionname0 | PRMT9_chr4_147637785_147684163 |
| regionname5000 | PRMT9_chr4_147632785_147689163 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 845 | 182 | 73 | 21 | 63 | 5 | 18 | 46 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0002 | 0/0 | 845 | 14 | 0 | 0 | 14 | 0 | 0 | 9 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0003 | 0/0 | 845 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0004 | 0/0 | 845 | 6 | 1 | 0 | 5 | 0 | 0 | 5 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0005 | 0/0 | 845 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0006 | 0/0 | 845 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0007 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0008 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0009 | 0/0 | 358 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0010 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0011 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2538 | 170 | 67 | 20 | 61 | 4 | 16 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0002 | 0/0 | 2538 | 14 | 0 | 0 | 14 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0003 | 0/0 | 2538 | 9 | 9 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0004 | 0/0 | 2538 | 6 | 1 | 0 | 5 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0005 | 0/0 | 2538 | 6 | 4 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0006 | 0/0 | 2538 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0007 | 0/0 | 2538 | 3 | 1 | 0 | 0 | 1 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0008 | 0/0 | 2538 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0009 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0010 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0011 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0012 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0013 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0014 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0015 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| c0016 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 924 | 157 | 72 | 16 | 49 | 4 | 15 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0002 | 0/0 | 924 | 47 | 8 | 1 | 34 | 1 | 3 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0003 | 0/0 | 924 | 5 | 5 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0004 | 0/0 | 924 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0005 | 0/0 | 924 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0006 | 0/0 | 920 | 2 | 0 | 1 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0007 | 1/0 | 924 | 2 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0008 | 0/0 | 924 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0009 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| t0010 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0004 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2538 | 170 | 67 | 20 | 61 | 4 | 16 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0005 | 0/0 | 2538 | 6 | 4 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0007 | 0/0 | 2538 | 3 | 1 | 0 | 0 | 1 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0010 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0012 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0013 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0002c0002 | 0/0 | 2538 | 14 | 0 | 0 | 14 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0003c0003 | 0/0 | 2538 | 9 | 9 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0004c0004 | 0/0 | 2538 | 6 | 1 | 0 | 5 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0005c0006 | 0/0 | 2538 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0006c0008 | 0/0 | 2538 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0007c0009 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0008c0016 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0009c0015 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0010c0014 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0011c0011 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3461 | 124 | 51 | 15 | 41 | 3 | 13 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0002 | 0/0 | 3461 | 32 | 8 | 1 | 19 | 1 | 3 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0003 | 0/0 | 3461 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0004 | 0/0 | 3461 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0006 | 0/0 | 3457 | 2 | 0 | 1 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0007 | 1/0 | 3461 | 2 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0008 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0001t0009 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0005t0001 | 0/0 | 3461 | 6 | 4 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0007t0001 | 0/0 | 3461 | 3 | 1 | 0 | 0 | 1 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0010t0001 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0012t0001 | 0/0 | 3461 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0001c0013t0001 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0002c0002t0002 | 0/0 | 3461 | 14 | 0 | 0 | 14 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0003c0003t0001 | 0/0 | 3461 | 9 | 9 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0004c0004t0001 | 0/0 | 3461 | 6 | 1 | 0 | 5 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0005c0006t0001 | 0/0 | 3461 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0006c0008t0005 | 0/0 | 3461 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0007c0009t0001 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0008c0016t0002 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0009c0015t0010 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0010c0014t0003 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| a0011c0011t0001 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | copy fasta | chr4 | 147632785 | 147689163 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0004 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0007g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0010t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0013t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0006c0008t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0006c0008t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0007c0009t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0008c0016t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0009c0015t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0010c0014t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0011c0011t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00735 | hp2 | a0001 | c0010 | t0001 | g0050 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01433 | hp1 | a0006 | c0008 | t0005 | g0090 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0068 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0108 | EUR | IBS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0099 | AMR | PEL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02027 | hp2 | a0001 | c0005 | t0001 | g0124 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02280 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0064 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02738 | hp1 | a0001 | c0012 | t0001 | g0120 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02818 | hp2 | a0005 | c0006 | t0001 | g0017 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02895 | hp1 | a0005 | c0006 | t0001 | g0021 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02896 | hp1 | a0011 | c0011 | t0001 | g0025 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02897 | hp2 | a0005 | c0006 | t0001 | g0015 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02976 | hp1 | a0005 | c0006 | t0001 | g0016 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0065 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0114 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0020 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0089 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03579 | hp1 | a0009 | c0015 | t0010 | g0191 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03831 | hp2 | a0001 | c0007 | t0001 | g0039 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18522 | hp2 | a0010 | c0014 | t0003 | g0153 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18943 | hp1 | a0004 | c0004 | t0001 | g0094 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18947 | hp1 | a0004 | c0004 | t0001 | g0055 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18948 | hp2 | a0004 | c0004 | t0001 | g0073 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18975 | hp2 | a0004 | c0004 | t0001 | g0093 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18982 | hp1 | a0004 | c0004 | t0001 | g0056 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18994 | hp2 | a0007 | c0009 | t0001 | g0010 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18997 | hp1 | a0001 | c0005 | t0001 | g0123 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19077 | hp1 | a0008 | c0016 | t0002 | g0205 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19240 | hp1 | a0001 | c0013 | t0001 | g0132 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0049 | AFR | ASW | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | TSI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20805 | hp2 | a0006 | c0008 | t0005 | g0062 | EUR | TSI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0107 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0030 | REF | REF | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147638741
|
C | T | 1 | a0004 | 6 | HG02280.hp1 NA18943.hp1 NA18947.hp1 others(3): Show |
missense_variant | MODERATE | c.2329G>A | p.Val777Ile | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 2505/3461 | 2329/2538 | 777/845 | chr4 | 147638741 | ||
| chr4:147639042
|
C | T | 1 | a0006 | 2 | HG01433.hp1 NA20805.hp2 |
missense_variant | MODERATE | c.2240G>A | p.Cys747Tyr | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 11/12 | 2416/3461 | 2240/2538 | 747/845 | chr4 | 147639042 | ||
| chr4:147639051
|
G | A | 1 | a0008 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2231C>T | p.Ser744Leu | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 11/12 | 2407/3461 | 2231/2538 | 744/845 | chr4 | 147639051 | ||
| chr4:147654450
|
T | C | 1 | a0005 | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.1447A>G | p.Ser483Gly | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/12 | 1623/3461 | 1447/2538 | 483/845 | chr4 | 147654450 | ||
| chr4:147654554
|
T | C | 1 | a0010 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1343A>G | p.Lys448Arg | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/12 | 1519/3461 | 1343/2538 | 448/845 | chr4 | 147654554 | ||
| chr4:147660917
|
G | A | 1 | a0009 | 1 | HG03579.hp1 | stop_gained | HIGH | c.1075C>T | p.Arg359* | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/12 | 1251/3461 | 1075/2538 | 359/845 | chr4 | 147660917 | ||
| chr4:147660982
|
C | G | 1 | a0011 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.1010G>C | p.Ser337Thr | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/12 | 1186/3461 | 1010/2538 | 337/845 | chr4 | 147660982 | ||
| chr4:147673026
|
C | T | 2 | a0003a0005 | 13 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
missense_variant | MODERATE | c.676G>A | p.Glu226Lys | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/12 | 852/3461 | 676/2538 | 226/845 | chr4 | 147673026 | ||
| chr4:147683948
|
C | A | 2 | a0002a0008 | 15 | HG00438.hp1 HG00609.hp1 HG02135.hp1 others(12): Show |
missense_variant | MODERATE | c.40G>T | p.Gly14Cys | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/12 | 216/3461 | 40/2538 | 14/845 | chr4 | 147683948 | ||
| chr4:147683950
|
C | G | 1 | a0007 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.38G>C | p.Gly13Ala | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/12 | 214/3461 | 38/2538 | 13/845 | chr4 | 147683950 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147638697
|
A | G | 1 | a0001c0005 | 6 | HG02027.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
synonymous_variant | LOW | c.2373T>C | p.His791His | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 2549/3461 | 2373/2538 | 791/845 | chr4 | 147638697 | ||
| chr4:147639059
|
G | A | 1 | a0001c0007 | 3 | HG01515.hp1 HG02559.hp2 HG03831.hp2 |
synonymous_variant | LOW | c.2223C>T | p.Asp741Asp | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 11/12 | 2399/3461 | 2223/2538 | 741/845 | chr4 | 147639059 | ||
| chr4:147653899
|
T | C | 1 | a0001c0013 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1998A>G | p.Pro666Pro | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/12 | 2174/3461 | 1998/2538 | 666/845 | chr4 | 147653899 | ||
| chr4:147654421
|
C | T | 1 | a0001c0012 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1476G>A | p.Ser492Ser | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/12 | 1652/3461 | 1476/2538 | 492/845 | chr4 | 147654421 | ||
| chr4:147673000
|
C | T | 1 | a0001c0010 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.702G>A | p.Thr234Thr | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/12 | 878/3461 | 702/2538 | 234/845 | chr4 | 147673000 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147637835
|
GATCA | G | 1 | a0001c0001t0006 | 2 | HG01981.hp2 NA18946.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693_*696delTGAT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 693 | chr4 | 147637835 | |||||
| chr4:147637905
|
C | T | 1 | a0009c0015t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*627G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 627 | chr4 | 147637905 | |||||
| chr4:147637985
|
G | T | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 220 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*547C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 547 | chr4 | 147637985 | |||||
| chr4:147638005
|
T | G | 1 | a0001c0001t0008 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 527 | chr4 | 147638005 | |||||
| chr4:147638102
|
A | T | 1 | a0001c0001t0004 | 4 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*430T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 430 | chr4 | 147638102 | |||||
| chr4:147638214
|
A | G | 1 | a0006c0008t0005 | 2 | HG01433.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*318T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 318 | chr4 | 147638214 | |||||
| chr4:147638252
|
G | A | 2 | a0001c0001t0003a0010c0014t0003 | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 12/12 | 280 | chr4 | 147638252 | |||||
| chr4:147684103
|
T | C | 2 | a0001c0001t0004a0001c0001t0009 | 5 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-116A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/12 | 116 | chr4 | 147684103 | |||||
| chr4:147684127
|
G | A | 4 | a0001c0001t0002a0002c0002t0002a0008c0016t0002others(1): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-140C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/12 | 140 | chr4 | 147684127 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147638934
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2322+26C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 11/11 | chr4 | 147638934 | ||||||
| chr4:147639206
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 221 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.2200-124G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147639206 | ||||||
| chr4:147639279
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2200-197C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147639279 | ||||||
| chr4:147639497
|
T | C | 18 | a0001c0001t0002g0008a0001c0001t0002g0169a0001c0001t0002g0172others(15): Show | 19 | HG02040.hp2 HG02071.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.2200-415A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147639497 | ||||||
| chr4:147639605
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2200-523C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147639605 | ||||||
| chr4:147639626
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2200-544G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147639626 | ||||||
| chr4:147640003
|
C | T | 3 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166 | 3 | HG01167.hp2 HG01169.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2200-921G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640003 | ||||||
| chr4:147640061
|
C | CT | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(50): Show | 55 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2200-980dupA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640061
|
C | CTT | 15 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 16 | HG00099.hp1 HG02135.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2200-981_2200-980d others(4): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640061
|
C | CTTTT | 43 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0133others(40): Show | 44 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2200-983_2200-980d others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640061
|
C | CTTTTT | 8 | a0001c0001t0001g0130a0001c0001t0002g0008a0001c0001t0002g0178others(5): Show | 9 | HG02040.hp2 HG02080.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2200-984_2200-980d others(7): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640061
|
CT | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0003g0154others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2200-980delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640061
|
CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0002g0009a0001c0001t0002g0175a0001c0001t0002g0188others(6): Show | 10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2200-993_2200-980d others(16): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | ||||||
| chr4:147640078
|
TTTTTTTT others(7): Show |
T | 7 | a0001c0001t0001g0069a0004c0004t0001g0018a0004c0004t0001g0055others(4): Show | 7 | HG01261.hp1 HG02280.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2200-1010_2200-997 others(17): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640078 | ||||||
| chr4:147640090
|
TA | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0145a0005c0006t0001g0015others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200-1009delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640090 | ||||||
| chr4:147640091
|
A | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 110 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2200-1009T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640091 | ||||||
| chr4:147640092
|
A | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 114 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2200-1010T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640092 | ||||||
| chr4:147640179
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2200-1097G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640179 | ||||||
| chr4:147640181
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2200-1099A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640181 | ||||||
| chr4:147640337
|
G | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.2200-1255C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640337 | ||||||
| chr4:147640589
|
T | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2200-1507A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640589 | ||||||
| chr4:147640593
|
C | T | 5 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200-1511G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640593 | ||||||
| chr4:147640623
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200-1541A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640623 | ||||||
| chr4:147640642
|
AACTATTC others(7): Show |
A | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2200-1574_2200-156 others(18): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640642 | ||||||
| chr4:147640789
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0036 | 3 | HG01884.hp2 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2200-1707A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640789 | ||||||
| chr4:147640815
|
G | T | 2 | a0001c0001t0002g0172a0001c0001t0002g0179 | 2 | NA18966.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2200-1733C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640815 | ||||||
| chr4:147640818
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.2200-1736G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640818 | ||||||
| chr4:147641015
|
C | T | 3 | a0003c0003t0001g0011a0003c0003t0001g0013a0003c0003t0001g0020 | 3 | HG02145.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2199+1772G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641015 | ||||||
| chr4:147641031
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2199+1756T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641031 | ||||||
| chr4:147641171
|
A | G | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG02572.hp2 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+1616T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641171 | ||||||
| chr4:147641366
|
T | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2199+1421A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641366 | ||||||
| chr4:147641607
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2199+1180G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641607 | ||||||
| chr4:147641738
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0053others(8): Show | 11 | HG00735.hp2 HG03704.hp2 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.2199+1049G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147641738 | ||||||
| chr4:147642013
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2199+774A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642013 | ||||||
| chr4:147642159
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2199+628C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642159 | ||||||
| chr4:147642374
|
GATTGCAG others(8): Show |
G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2199+398_2199+412d others(17): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642374 | ||||||
| chr4:147642376
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0091 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.2199+411A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642376 | ||||||
| chr4:147642528
|
A | AC | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 200 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.2199+258dupG | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642528 | ||||||
| chr4:147642716
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2199+71T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642716 | ||||||
| chr4:147642769
|
TCTC | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2199+15_2199+17del others(3): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642769 | ||||||
| chr4:147643032
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046-92C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147643032 | ||||||
| chr4:147643081
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2046-141C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147643081 | ||||||
| chr4:147643210
|
T | G | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.2046-270A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147643210 | ||||||
| chr4:147643218
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2046-278G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147643218 | ||||||
| chr4:147643662
|
T | C | 1 | a0001c0001t0007g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2046-722A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147643662 | ||||||
| chr4:147644371
|
T | A | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2046-1431A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644371 | ||||||
| chr4:147644373
|
T | TA | 69 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(66): Show | 72 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(69): Show |
intron_variant | MODIFIER | c.2046-1434dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644373 | ||||||
| chr4:147644373
|
TA | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2046-1434delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644373 | ||||||
| chr4:147644539
|
T | TA | 85 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0022others(82): Show | 88 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(85): Show |
intron_variant | MODIFIER | c.2046-1600dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644539 | ||||||
| chr4:147644539
|
T | TAA | 96 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0019others(93): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2046-1601_2046-160 others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644539 | ||||||
| chr4:147644539
|
T | TAAA | 6 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0057others(3): Show | 7 | HG04228.hp2 NA18950.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2046-1602_2046-160 others(7): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644539 | ||||||
| chr4:147644999
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2046-2059T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644999 | ||||||
| chr4:147645136
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2046-2196G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147645136 | ||||||
| chr4:147645282
|
A | ATTATCTC others(4): Show |
1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046-2353_2046-234 others(15): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147645282 | ||||||
| chr4:147645312
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0106others(3): Show | 6 | HG00642.hp2 HG01515.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2046-2372A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147645312 | ||||||
| chr4:147645583
|
G | C | 1 | a0001c0005t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2046-2643C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147645583 | ||||||
| chr4:147646192
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046-3252C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646192 | ||||||
| chr4:147646662
|
A | AG | 52 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0037others(49): Show | 53 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.2046-3723dupC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646662 | ||||||
| chr4:147646673
|
G | A | 7 | a0001c0001t0001g0019a0001c0005t0001g0064a0001c0005t0001g0065others(4): Show | 7 | HG02027.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2046-3733C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646673 | ||||||
| chr4:147646845
|
G | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2046-3905C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646845 | ||||||
| chr4:147646882
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2046-3942A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646882 | ||||||
| chr4:147646945
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046-4005G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147646945 | ||||||
| chr4:147647130
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2046-4190C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647130 | ||||||
| chr4:147647618
|
G | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2046-4678C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647618 | ||||||
| chr4:147647988
|
CG | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2046-5049delC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647988 | ||||||
| chr4:147648163
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2046-5223G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147648163 | ||||||
| chr4:147648227
|
G | A | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.2046-5287C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147648227 | ||||||
| chr4:147648943
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2045+4909T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147648943 | ||||||
| chr4:147649138
|
C | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.2045+4714G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649138 | ||||||
| chr4:147649150
|
C | CAG | 3 | a0001c0001t0002g0172a0001c0001t0002g0179a0001c0001t0002g0180 | 3 | NA18966.hp1 NA18979.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2045+4700_2045+470 others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649150 | ||||||
| chr4:147649297
|
A | G | 6 | a0004c0004t0001g0018a0004c0004t0001g0055a0004c0004t0001g0056others(3): Show | 6 | HG02280.hp1 NA18943.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.2045+4555T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649297 | ||||||
| chr4:147649424
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2045+4428G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649424 | ||||||
| chr4:147649565
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2045+4287G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649565 | ||||||
| chr4:147649566
|
G | A | 2 | a0001c0001t0002g0009a0001c0001t0002g0175 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2045+4286C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649566 | ||||||
| chr4:147649659
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2045+4193G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649659 | ||||||
| chr4:147649735
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2045+4117G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649735 | ||||||
| chr4:147649838
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2045+4014G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649838 | ||||||
| chr4:147649948
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2045+3904G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147649948 | ||||||
| chr4:147650048
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2045+3804C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650048 | ||||||
| chr4:147650128
|
G | T | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.2045+3724C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650128 | ||||||
| chr4:147650561
|
T | A | 1 | a0001c0005t0001g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2045+3291A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650561 | ||||||
| chr4:147650567
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2045+3285G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650567 | ||||||
| chr4:147650721
|
T | C | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045+3131A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650721 | ||||||
| chr4:147650840
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2045+3012A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650840 | ||||||
| chr4:147650885
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2045+2967T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650885 | ||||||
| chr4:147650899
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2045+2953C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650899 | ||||||
| chr4:147650937
|
T | C | 2 | a0006c0008t0005g0062a0006c0008t0005g0090 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2045+2915A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147650937 | ||||||
| chr4:147651026
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2045+2826G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651026 | ||||||
| chr4:147651102
|
C | CA | 6 | a0001c0001t0001g0129a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2045+2749dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651102 | ||||||
| chr4:147651129
|
T | A | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045+2723A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651129 | ||||||
| chr4:147651430
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2045+2422A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651430 | ||||||
| chr4:147651445
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2045+2407C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651445 | ||||||
| chr4:147651446
|
G | A | 3 | a0003c0003t0001g0001a0003c0003t0001g0048a0003c0003t0001g0049 | 5 | HG01891.hp1 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045+2406C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651446 | ||||||
| chr4:147651451
|
C | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2045+2401G>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651451 | ||||||
| chr4:147651492
|
T | C | 1 | a0001c0005t0001g0123 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2045+2360A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651492 | ||||||
| chr4:147651551
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2045+2301C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651551 | ||||||
| chr4:147651632
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036 | 4 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2045+2220T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651632 | ||||||
| chr4:147651696
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2045+2156C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651696 | ||||||
| chr4:147651768
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2045+2084C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147651768 | ||||||
| chr4:147652036
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2045+1816C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652036 | ||||||
| chr4:147652070
|
C | T | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.2045+1782G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652070 | ||||||
| chr4:147652454
|
C | CA | 36 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0042others(33): Show | 38 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.2045+1397dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652454 | ||||||
| chr4:147652457
|
A | AC | 2 | a0001c0001t0001g0066a0001c0001t0006g0099 | 2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2045+1394_2045+139 others(5): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652457 | ||||||
| chr4:147652650
|
C | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.2045+1202G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652650 | ||||||
| chr4:147652711
|
T | TA | 28 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0109others(25): Show | 29 | HG00438.hp2 HG02027.hp1 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.2045+1140dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652711 | ||||||
| chr4:147652711
|
T | TAA | 5 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0159others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045+1139_2045+114 others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652711 | ||||||
| chr4:147652724
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0013t0001g0132 | 3 | HG03225.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2045+1128G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652724 | ||||||
| chr4:147652732
|
CA | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(188): Show | 199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.2045+1119delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652732 | ||||||
| chr4:147652769
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2045+1083C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652769 | ||||||
| chr4:147652796
|
A | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2045+1056T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652796 | ||||||
| chr4:147652951
|
A | G | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045+901T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652951 | ||||||
| chr4:147652975
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2045+877A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147652975 | ||||||
| chr4:147653042
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0106others(3): Show | 6 | HG00642.hp2 HG01515.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2045+810A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653042 | ||||||
| chr4:147653442
|
TA | T | 55 | a0001c0001t0001g0024a0001c0001t0001g0129a0001c0001t0001g0143others(52): Show | 57 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(54): Show |
intron_variant | MODIFIER | c.2045+409delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653442 | ||||||
| chr4:147653451
|
A | AT | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2045+400_2045+401i others(3): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653451 | ||||||
| chr4:147653451
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2045+401T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653451 | ||||||
| chr4:147653453
|
A | AT | 3 | a0001c0001t0001g0042a0001c0001t0001g0122a0001c0010t0001g0050 | 3 | HG00735.hp2 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2045+398_2045+399i others(3): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653453 | ||||||
| chr4:147653453
|
A | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0080a0001c0001t0001g0092others(58): Show | 64 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.2045+399T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653453 | ||||||
| chr4:147653454
|
AT | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(67): Show | 74 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(71): Show |
intron_variant | MODIFIER | c.2045+397delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653454 | ||||||
| chr4:147653455
|
T | A | 1 | a0001c0001t0001g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2045+397A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653455 | ||||||
| chr4:147653552
|
G | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2045+300C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653552 | ||||||
| chr4:147653810
|
C | CA | 6 | a0001c0001t0001g0130a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2045+41dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653810 | ||||||
| chr4:147655034
|
C | T | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331-468G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655034 | ||||||
| chr4:147655114
|
A | G | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331-548T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655114 | ||||||
| chr4:147655430
|
T | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1331-864A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655430 | ||||||
| chr4:147655575
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1331-1009A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655575 | ||||||
| chr4:147655582
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1331-1016G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655582 | ||||||
| chr4:147655819
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331-1253T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655819 | ||||||
| chr4:147655856
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.1331-1290A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655856 | ||||||
| chr4:147655899
|
ATCTG | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1331-1337_1331-133 others(8): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655899 | ||||||
| chr4:147656017
|
A | T | 1 | a0004c0004t0001g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1331-1451T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656017 | ||||||
| chr4:147656040
|
G | C | 1 | a0002c0002t0002g0201 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1331-1474C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656040 | ||||||
| chr4:147656181
|
C | A | 1 | a0011c0011t0001g0025 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1330+1611G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656181 | ||||||
| chr4:147656289
|
CTG | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.1330+1501_1330+150 others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656289 | ||||||
| chr4:147656500
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG03225.hp1 HG03486.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1330+1292G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656500 | ||||||
| chr4:147656568
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1330+1224G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656568 | ||||||
| chr4:147656715
|
T | G | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1330+1077A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656715 | ||||||
| chr4:147656771
|
C | CA | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1330+1020dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656771 | ||||||
| chr4:147656771
|
CA | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0138others(4): Show | 7 | HG02040.hp2 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330+1020delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656771 | ||||||
| chr4:147656771
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1330+1011_1330+102 others(14): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656771 | ||||||
| chr4:147656771
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0121 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1330+1009_1330+102 others(16): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656771 | ||||||
| chr4:147657010
|
A | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1330+782T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657010 | ||||||
| chr4:147657175
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1330+617A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657175 | ||||||
| chr4:147657280
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1330+512G>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657280 | ||||||
| chr4:147657292
|
G | A | 1 | a0001c0005t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1330+500C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657292 | ||||||
| chr4:147657308
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1330+484C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657308 | ||||||
| chr4:147657398
|
G | A | 3 | a0003c0003t0001g0011a0003c0003t0001g0013a0003c0003t0001g0020 | 3 | HG02145.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1330+394C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657398 | ||||||
| chr4:147657451
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 12 | HG00438.hp2 HG00609.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1330+341C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657451 | ||||||
| chr4:147657457
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1330+335C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657457 | ||||||
| chr4:147657515
|
C | T | 1 | a0001c0001t0002g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1330+277G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657515 | ||||||
| chr4:147657628
|
T | G | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1330+164A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657628 | ||||||
| chr4:147657659
|
T | A | 1 | a0001c0001t0002g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1330+133A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147657659 | ||||||
| chr4:147658081
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1147-106G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658081 | ||||||
| chr4:147658241
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1147-266A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658241 | ||||||
| chr4:147658339
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1147-364T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658339 | ||||||
| chr4:147658347
|
AAGAG | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1147-376_1147-373d others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658347 | ||||||
| chr4:147658497
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1147-522T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658497 | ||||||
| chr4:147658539
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-564A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658539 | ||||||
| chr4:147658540
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-565A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658540 | ||||||
| chr4:147658541
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-566C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658541 | ||||||
| chr4:147658544
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-569T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658544 | ||||||
| chr4:147658545
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-570A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658545 | ||||||
| chr4:147658546
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1147-571A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658546 | ||||||
| chr4:147658871
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1147-896C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658871 | ||||||
| chr4:147658907
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1147-932G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658907 | ||||||
| chr4:147658961
|
C | T | 11 | a0003c0003t0001g0001a0003c0003t0001g0011a0003c0003t0001g0013others(8): Show | 13 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1147-986G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658961 | ||||||
| chr4:147658962
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1147-987C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147658962 | ||||||
| chr4:147659006
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1147-1031G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659006 | ||||||
| chr4:147659072
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1147-1097C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659072 | ||||||
| chr4:147659178
|
C | CA | 28 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 29 | HG02055.hp2 HG02135.hp1 HG02572.hp2 others(26): Show |
intron_variant | MODIFIER | c.1147-1204dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659178 | ||||||
| chr4:147659198
|
C | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1147-1223G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659198 | ||||||
| chr4:147659231
|
T | C | 3 | a0003c0003t0001g0011a0003c0003t0001g0013a0003c0003t0001g0020 | 3 | HG02145.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1147-1256A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659231 | ||||||
| chr4:147659316
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 221 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1147-1341T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659316 | ||||||
| chr4:147659573
|
TC | T | 43 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(40): Show | 45 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.1146+1272delG | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659573 | ||||||
| chr4:147659574
|
C | T | 3 | a0001c0001t0002g0175a0001c0001t0002g0185a0001c0001t0002g0195 | 3 | HG02145.hp1 NA19078.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1146+1272G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659574 | ||||||
| chr4:147659575
|
T | C | 3 | a0001c0001t0002g0175a0001c0001t0002g0185a0001c0001t0002g0195 | 3 | HG02145.hp1 NA19078.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1146+1271A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659575 | ||||||
| chr4:147659576
|
T | C | 43 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(40): Show | 45 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.1146+1270A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659576 | ||||||
| chr4:147659576
|
T | TTTC | 14 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0034others(11): Show | 15 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1146+1267_1146+126 others(7): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659576 | ||||||
| chr4:147659578
|
T | C | 3 | a0001c0001t0002g0175a0001c0001t0002g0185a0001c0001t0002g0195 | 3 | HG02145.hp1 NA19078.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1146+1268A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659578 | ||||||
| chr4:147659579
|
C | CTTT | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.1146+1264_1146+126 others(7): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659579 | ||||||
| chr4:147659579
|
C | CTTTT | 28 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0042others(25): Show | 29 | HG01261.hp1 HG01433.hp2 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.1146+1263_1146+126 others(8): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659579 | ||||||
| chr4:147659579
|
C | T | 3 | a0001c0001t0002g0175a0001c0001t0002g0185a0001c0001t0002g0195 | 3 | HG02145.hp1 NA19078.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1146+1267G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659579 | ||||||
| chr4:147659594
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1146+1252G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659594 | ||||||
| chr4:147659709
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036 | 4 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+1137G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659709 | ||||||
| chr4:147659743
|
A | G | 16 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(13): Show | 18 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1146+1103T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659743 | ||||||
| chr4:147659833
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1146+1013C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659833 | ||||||
| chr4:147659844
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1146+1002C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147659844 | ||||||
| chr4:147660062
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1146+784C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660062 | ||||||
| chr4:147660248
|
G | C | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+598C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660248 | ||||||
| chr4:147660436
|
C | T | 4 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+410G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660436 | ||||||
| chr4:147660487
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1146+359C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660487 | ||||||
| chr4:147660708
|
A | G | 1 | a0001c0001t0006g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1146+138T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660708 | ||||||
| chr4:147660709
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1146+137G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 7/11 | chr4 | 147660709 | ||||||
| chr4:147661042
|
G | T | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
splice_region_variant&intron_variant | LOW | c.954-4C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661042 | ||||||
| chr4:147661261
|
TA | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 82 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.954-224delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661261 | ||||||
| chr4:147661345
|
T | C | 2 | a0006c0008t0005g0062a0006c0008t0005g0090 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.954-307A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661345 | ||||||
| chr4:147661538
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.954-500G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661538 | ||||||
| chr4:147661547
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.954-509A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661547 | ||||||
| chr4:147661673
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.954-635G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661673 | ||||||
| chr4:147661747
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.954-709C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661747 | ||||||
| chr4:147661777
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954-739C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661777 | ||||||
| chr4:147661789
|
C | CA | 26 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0067others(23): Show | 27 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(24): Show |
intron_variant | MODIFIER | c.954-752dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661789 | ||||||
| chr4:147661789
|
C | CAA | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 112 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.954-753_954-752dup others(2): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661789 | ||||||
| chr4:147661789
|
C | CAAA | 45 | a0001c0001t0001g0044a0001c0001t0001g0092a0001c0001t0001g0097others(42): Show | 47 | HG00609.hp1 HG01106.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.954-754_954-752dup others(3): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661789 | ||||||
| chr4:147661789
|
C | CAAAA | 13 | a0001c0001t0001g0095a0001c0001t0001g0162a0001c0001t0002g0171others(10): Show | 13 | HG00438.hp1 HG01243.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.954-755_954-752dup others(4): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661789 | ||||||
| chr4:147661814
|
T | A | 45 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(42): Show | 47 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.954-776A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661814 | ||||||
| chr4:147661960
|
G | A | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.954-922C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661960 | ||||||
| chr4:147662140
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.954-1102C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662140 | ||||||
| chr4:147662157
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.954-1119A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662157 | ||||||
| chr4:147662408
|
G | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.954-1370C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662408 | ||||||
| chr4:147662848
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.954-1810A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662848 | ||||||
| chr4:147663006
|
A | C | 1 | a0001c0005t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.954-1968T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663006 | ||||||
| chr4:147663009
|
A | AT | 14 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0121others(11): Show | 14 | HG00609.hp1 HG02135.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.954-1972dupA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663009 | ||||||
| chr4:147663230
|
G | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.954-2192C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663230 | ||||||
| chr4:147663251
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.954-2213C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663251 | ||||||
| chr4:147663297
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.954-2259G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663297 | ||||||
| chr4:147663321
|
A | G | 2 | a0003c0003t0001g0011a0003c0003t0001g0013 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.954-2283T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663321 | ||||||
| chr4:147663663
|
G | T | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-2625C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147663663 | ||||||
| chr4:147664118
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0097others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.954-3080C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147664118 | ||||||
| chr4:147664257
|
A | G | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-3219T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147664257 | ||||||
| chr4:147664723
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.954-3685G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147664723 | ||||||
| chr4:147664830
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0187 | 2 | HG02040.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.953+3709T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147664830 | ||||||
| chr4:147664890
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.953+3649T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147664890 | ||||||
| chr4:147665117
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.953+3422C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665117 | ||||||
| chr4:147665124
|
C | CA | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 180 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.953+3414dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665124 | ||||||
| chr4:147665124
|
C | CAA | 10 | a0001c0001t0001g0044a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.953+3413_953+3414d others(4): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665124 | ||||||
| chr4:147665382
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.953+3157A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665382 | ||||||
| chr4:147665490
|
G | C | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.953+3049C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665490 | ||||||
| chr4:147665491
|
T | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.953+3048A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665491 | ||||||
| chr4:147665595
|
A | T | 1 | a0001c0001t0002g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.953+2944T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665595 | ||||||
| chr4:147665654
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.953+2885C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665654 | ||||||
| chr4:147665847
|
C | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.953+2692G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665847 | ||||||
| chr4:147666032
|
T | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.953+2507A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666032 | ||||||
| chr4:147666074
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.953+2465G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666074 | ||||||
| chr4:147666300
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0117 | 2 | HG02027.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.953+2239C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666300 | ||||||
| chr4:147666579
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.953+1960C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666579 | ||||||
| chr4:147666600
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(3): Show | 7 | HG02055.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.953+1939A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666600 | ||||||
| chr4:147666769
|
T | G | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.953+1770A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666769 | ||||||
| chr4:147666823
|
T | TA | 71 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0121others(68): Show | 74 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(71): Show |
intron_variant | MODIFIER | c.953+1715dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666823 | ||||||
| chr4:147666823
|
TA | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(21): Show | 25 | HG00099.hp2 HG00735.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.953+1715delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666823 | ||||||
| chr4:147666869
|
C | A | 1 | a0002c0002t0002g0209 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.953+1670G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666869 | ||||||
| chr4:147666869
|
C | T | 1 | a0004c0004t0001g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.953+1670G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147666869 | ||||||
| chr4:147667379
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.953+1160T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147667379 | ||||||
| chr4:147667442
|
C | A | 15 | a0002c0002t0002g0198a0002c0002t0002g0199a0002c0002t0002g0200others(12): Show | 15 | HG00438.hp1 HG00609.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.953+1097G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147667442 | ||||||
| chr4:147667538
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.953+1001A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147667538 | ||||||
| chr4:147667734
|
GA | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.953+804delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147667734 | ||||||
| chr4:147668001
|
A | AAAG | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 191 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.953+537_953+538ins others(3): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147668001 | ||||||
| chr4:147668326
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0163 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.953+213C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147668326 | ||||||
| chr4:147668339
|
G | GTC | 5 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0106others(2): Show | 5 | HG00642.hp2 HG01515.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+198_953+199dup others(2): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147668339 | ||||||
| chr4:147668526
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.953+13G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147668526 | ||||||
| chr4:147668661
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0109 | 2 | NA18979.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.847-16T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147668661 | ||||||
| chr4:147668716
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.847-71A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147668716 | ||||||
| chr4:147669002
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.847-357G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669002 | ||||||
| chr4:147669086
|
T | TA | 5 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 6 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-442dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669086 | ||||||
| chr4:147669160
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.847-515C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669160 | ||||||
| chr4:147669225
|
C | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0163 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.847-580G>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669225 | ||||||
| chr4:147669235
|
AT | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.847-591delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669235 | ||||||
| chr4:147669236
|
TG | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 145 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.847-592delC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669236 | ||||||
| chr4:147669237
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.847-592C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669237 | ||||||
| chr4:147669295
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036 | 4 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-650C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669295 | ||||||
| chr4:147669301
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.847-656C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669301 | ||||||
| chr4:147669323
|
C | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.847-678G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669323 | ||||||
| chr4:147669373
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.847-728A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669373 | ||||||
| chr4:147669378
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.847-733T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669378 | ||||||
| chr4:147669505
|
A | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.847-860T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669505 | ||||||
| chr4:147669545
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.847-900A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669545 | ||||||
| chr4:147669570
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.847-925C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669570 | ||||||
| chr4:147669584
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.847-939C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669584 | ||||||
| chr4:147669963
|
A | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.846+678T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669963 | ||||||
| chr4:147670165
|
GTTGTT | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 219 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.846+471_846+475del others(5): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670165 | ||||||
| chr4:147670165
|
GTTGTTTT others(3): Show |
G | 1 | a0001c0001t0002g0186 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.846+466_846+475del others(10): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670165 | ||||||
| chr4:147670394
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02615.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.846+247C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670394 | ||||||
| chr4:147670399
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.846+242C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670399 | ||||||
| chr4:147670618
|
G | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.846+23C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670618 | ||||||
| chr4:147670837
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.744-94A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147670837 | ||||||
| chr4:147670979
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.744-236C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147670979 | ||||||
| chr4:147671437
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.744-694A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147671437 | ||||||
| chr4:147671477
|
A | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.744-734T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147671477 | ||||||
| chr4:147671747
|
T | C | 1 | a0001c0001t0002g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.744-1004A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147671747 | ||||||
| chr4:147671947
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+1012C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147671947 | ||||||
| chr4:147671961
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.743+998G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147671961 | ||||||
| chr4:147672171
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743+788C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672171 | ||||||
| chr4:147672186
|
C | T | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.743+773G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672186 | ||||||
| chr4:147672209
|
T | C | 9 | a0001c0001t0002g0009a0001c0001t0002g0175a0001c0001t0002g0188others(6): Show | 10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+750A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672209 | ||||||
| chr4:147672227
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.743+732A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672227 | ||||||
| chr4:147672232
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.743+727C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672232 | ||||||
| chr4:147672454
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.743+505C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672454 | ||||||
| chr4:147672454
|
G | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.743+505C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672454 | ||||||
| chr4:147672661
|
C | T | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+298G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672661 | ||||||
| chr4:147673140
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.576-14T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 3/11 | chr4 | 147673140 | ||||||
| chr4:147673215
|
T | G | 1 | a0003c0003t0001g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.576-89A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 3/11 | chr4 | 147673215 | ||||||
| chr4:147673498
|
AC | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.575+139delG | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 3/11 | chr4 | 147673498 | ||||||
| chr4:147673962
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.339-88C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147673962 | ||||||
| chr4:147674334
|
G | A | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | HG01261.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.339-460C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147674334 | ||||||
| chr4:147674374
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339-500G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147674374 | ||||||
| chr4:147674575
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.339-701G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147674575 | ||||||
| chr4:147674856
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-982G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147674856 | ||||||
| chr4:147675084
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.339-1210C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147675084 | ||||||
| chr4:147675270
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339-1396C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147675270 | ||||||
| chr4:147676070
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.339-2196A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676070 | ||||||
| chr4:147676301
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.339-2427G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676301 | ||||||
| chr4:147676421
|
C | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.339-2547G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676421 | ||||||
| chr4:147676632
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.339-2758A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676632 | ||||||
| chr4:147676794
|
G | A | 1 | a0001c0005t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.339-2920C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676794 | ||||||
| chr4:147676809
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.339-2935G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676809 | ||||||
| chr4:147676846
|
C | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0144others(1): Show | 4 | HG03704.hp2 NA18968.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-2972G>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676846 | ||||||
| chr4:147676917
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.339-3043C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676917 | ||||||
| chr4:147676938
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.339-3064C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147676938 | ||||||
| chr4:147677038
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.339-3164G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677038 | ||||||
| chr4:147677043
|
C | CA | 13 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0117others(10): Show | 13 | HG00438.hp2 HG00642.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.339-3170dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677043 | ||||||
| chr4:147677043
|
CA | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0128a0001c0001t0001g0129others(48): Show | 53 | HG00609.hp1 HG01261.hp2 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.339-3170delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677043 | ||||||
| chr4:147677122
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.338+3201C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677122 | ||||||
| chr4:147677445
|
A | AT | 17 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0032others(14): Show | 19 | HG02055.hp1 HG02071.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.338+2877dupA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677445 | ||||||
| chr4:147677445
|
AT | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 112 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.338+2877delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677445 | ||||||
| chr4:147677445
|
ATT | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0148others(4): Show | 7 | HG02027.hp2 HG02080.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.338+2876_338+2877d others(4): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677445 | ||||||
| chr4:147677825
|
G | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.338+2498C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677825 | ||||||
| chr4:147678089
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.338+2234G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678089 | ||||||
| chr4:147678139
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.338+2184A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678139 | ||||||
| chr4:147678325
|
TTAAC | T | 5 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+1994_338+1997d others(6): Show |
PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678325 | ||||||
| chr4:147678349
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 26 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.338+1974C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678349 | ||||||
| chr4:147678480
|
A | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.338+1843T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678480 | ||||||
| chr4:147678561
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.338+1762C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678561 | ||||||
| chr4:147678863
|
T | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.338+1460A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678863 | ||||||
| chr4:147679148
|
G | A | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.338+1175C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679148 | ||||||
| chr4:147679291
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338+1032G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679291 | ||||||
| chr4:147679321
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.338+1002C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679321 | ||||||
| chr4:147679445
|
CA | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 10 | HG02055.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.338+877delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679445 | ||||||
| chr4:147679545
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.338+778G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679545 | ||||||
| chr4:147679549
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.338+774T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679549 | ||||||
| chr4:147679698
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.338+625A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679698 | ||||||
| chr4:147679722
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.338+601G>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679722 | ||||||
| chr4:147679888
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338+435G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679888 | ||||||
| chr4:147679900
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.338+423A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679900 | ||||||
| chr4:147679939
|
A | G | 1 | a0001c0007t0001g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.338+384T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679939 | ||||||
| chr4:147679990
|
A | G | 46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0169others(43): Show | 48 | HG00438.hp1 HG00609.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.338+333T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147679990 | ||||||
| chr4:147680578
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.190-107G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147680578 | ||||||
| chr4:147680609
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-138C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147680609 | ||||||
| chr4:147680969
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.190-498G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147680969 | ||||||
| chr4:147681315
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190-844G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681315 | ||||||
| chr4:147681440
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.190-969C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681440 | ||||||
| chr4:147681541
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0013t0001g0132 | 3 | HG03225.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.190-1070G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681541 | ||||||
| chr4:147681594
|
A | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.190-1123T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681594 | ||||||
| chr4:147681616
|
A | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.190-1145T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681616 | ||||||
| chr4:147681764
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-1293C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681764 | ||||||
| chr4:147681776
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01891.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.190-1305C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681776 | ||||||
| chr4:147681783
|
TA | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 144 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.190-1313delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681783 | ||||||
| chr4:147681797
|
A | C | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-1326T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681797 | ||||||
| chr4:147682062
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.190-1591T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682062 | ||||||
| chr4:147682370
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189+1429C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682370 | ||||||
| chr4:147682401
|
A | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.189+1398T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682401 | ||||||
| chr4:147682422
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+1377G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682422 | ||||||
| chr4:147682465
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189+1334G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682465 | ||||||
| chr4:147682997
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02809.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.189+802C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682997 | ||||||
| chr4:147683000
|
A | G | 6 | a0001c0001t0001g0034a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+799T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683000 | ||||||
| chr4:147683125
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.189+674T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683125 | ||||||
| chr4:147683421
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 16 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.189+378A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683421 | ||||||
| chr4:147683720
|
CT | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG02055.hp1 HG02080.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+78delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683720 | ||||||
| chr4:147683732
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189+67A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683732 | ||||||
| chr4:147683733
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189+66G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683733 | ||||||
| chr4:147683734
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189+65A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683734 | ||||||
| chr4:147683734
|
T | TA | 11 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0002g0169others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+64_189+65insT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683734 | ||||||
| chr4:147683734
|
TG | T | 15 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0158others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+64delC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683734 | ||||||
| chr4:147683735
|
G | A | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 182 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.189+64C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683735 | ||||||
| chr4:147683735
|
G | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(10): Show | 13 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+64C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683735 | ||||||
| chr4:147683736
|
T | A | 15 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0158others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+63A>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147683736 |