Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0002 | 0/0 | 845 | 14 | 0 | 0 | 14 | 0 | 0 | 9 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0003 | 0/0 | 845 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0004 | 0/0 | 845 | 6 | 1 | 0 | 5 | 0 | 0 | 5 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0005 | 0/0 | 845 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0006 | 0/0 | 845 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0007 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0008 | 0/0 | 358 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(353): Show |
chr4 | 147632785 | 147689163 |
| a0009 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0010 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| a0011 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | MSNSR others(840): Show |
chr4 | 147632785 | 147689163 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2535 | 170 | 67 | 20 | 61 | 4 | 16 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0001c0005 | 0/0 | 2535 | 6 | 4 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0001c0007 | 0/0 | 2535 | 3 | 1 | 0 | 0 | 1 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0001c0010 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0001c0012 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0001c0013 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0002c0002 | 0/0 | 2535 | 14 | 0 | 0 | 14 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0003c0003 | 0/0 | 2535 | 9 | 9 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0004c0004 | 0/0 | 2535 | 6 | 1 | 0 | 5 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0005c0006 | 0/0 | 2535 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0006c0008 | 0/0 | 2535 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0007c0011 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0008c0015 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0009c0014 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0010c0009 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
chr4 | 147632785 | 147689163 | ||
| a0011c0016 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | ATGTC others(2530): Show |
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 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0002 | 0/0 | 3461 | 32 | 8 | 1 | 19 | 1 | 3 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0003 | 0/0 | 3461 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0004 | 0/0 | 3461 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0006 | 0/0 | 3457 | 2 | 0 | 1 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3452): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0007 | 1/0 | 3461 | 2 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0008 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0001t0009 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0005t0001 | 0/0 | 3461 | 6 | 4 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0007t0001 | 0/0 | 3461 | 3 | 1 | 0 | 0 | 1 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0010t0001 | 0/0 | 3461 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0012t0001 | 0/0 | 3461 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0001c0013t0001 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0002c0002t0002 | 0/0 | 3461 | 14 | 0 | 0 | 14 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0003c0003t0001 | 0/0 | 3461 | 9 | 9 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0004c0004t0001 | 0/0 | 3461 | 6 | 1 | 0 | 5 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0005c0006t0001 | 0/0 | 3461 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0006c0008t0005 | 0/0 | 3461 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0007c0011t0001 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0008c0015t0010 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0009c0014t0003 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0010c0009t0001 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| a0011c0016t0002 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | AGGAC others(3456): Show |
chr4 | 147632785 | 147689163 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 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 | 0/0 | 2 | 0 | 0 | 2 | 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 | 2 | 0 | 0 | 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 |
| a0001c0001t0001g0015 | 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 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| 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 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0001g0154 | 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 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 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 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0007g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0010t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0001c0012t0001g0111 | 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 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0002c0002t0002g0205 | 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 |
| a0003c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0003c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0004c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0005c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0006c0008t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0006c0008t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0007c0011t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0008c0015t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0009c0014t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0010c0009t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| a0011c0016t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0031 | EUR | GBR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG00735 | hp2 | a0001 | c0010 | t0001 | g0043 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01433 | hp1 | a0006 | c0008 | t0005 | g0081 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0061 | AMR | CLM | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0099 | EUR | IBS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0106 | 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 | g0059 | AMR | PEL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0090 | AMR | PEL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02027 | hp2 | a0001 | c0005 | t0001 | g0115 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0172 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | 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 | g0010 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | CDX | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02280 | hp1 | a0004 | c0004 | t0001 | g0021 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0057 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0193 | 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 | g0012 | 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 | g0022 | 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 | g0008 | 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 | g0119 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02738 | hp1 | a0001 | c0012 | t0001 | g0111 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02818 | hp2 | a0005 | c0006 | t0001 | g0020 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02895 | hp1 | a0005 | c0006 | t0001 | g0024 | 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 | a0007 | c0011 | t0001 | g0122 | 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 | g0018 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0001 | 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 | g0019 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0033 | 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 | g0025 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0105 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | 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 | g0023 | 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 | g0012 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0186 | 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 | g0060 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | 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 | g0080 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03579 | hp1 | a0008 | c0015 | t0010 | g0187 | 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 | g0097 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG03831 | hp2 | a0001 | c0007 | t0001 | g0032 | SAS | BEB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0169 | 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 | g0113 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18522 | hp2 | a0009 | c0014 | t0003 | g0155 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0120 | 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 | g0085 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18947 | hp1 | a0004 | c0004 | t0001 | g0048 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18948 | hp2 | a0004 | c0004 | t0001 | g0066 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18975 | hp2 | a0004 | c0004 | t0001 | g0084 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18982 | hp1 | a0004 | c0004 | t0001 | g0049 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0167 | 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 | g0072 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0153 | 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 | a0010 | c0009 | t0001 | g0014 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18997 | hp1 | a0001 | c0005 | t0001 | g0114 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0112 | 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 | a0011 | c0016 | t0002 | g0199 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0013 | 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 | g0077 | AFR | YRI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0042 | 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 | g0184 | EUR | TSI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20805 | hp2 | a0006 | c0008 | t0005 | g0055 | EUR | TSI | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0166 | 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 | g0011 | AFR | ACB | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0098 | 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 | g0188 | AFR | MSL | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | 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 | g0015 | AFR | LWK | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0152 | REF | REF | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0127 | REF | REF | PRMT9_chr4_147632785_147689163 | PRMT9 | chr4 | 147632785 | 147689163 |
| view | 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 | a0011 | 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 | a0009 | 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 | a0008 | 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 | a0007 | 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 | a0003 a0005 |
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 | a0002 a0011 |
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 | a0010 | 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 |
| view | 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 |
| view | 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 | a0008c0015t0010 | 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
219 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(216): 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 | a0001c0001t0003 a0009c0014t0003 |
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 | a0001c0001t0004 a0001c0001t0009 |
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 | a0001c0001t0002 a0002c0002t0002 a0008c0015t0010 others(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 |
| view | 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 | a0001c0001t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2322+26C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 11/11 | chr4 | 147638934 | |||||||
| chr4:147639279 | G | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0002g0010 a0001c0001t0002g0167 a0001c0001t0002g0170 others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0034 | 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 | 2 | a0001c0001t0004g0009 a0001c0001t0004g0164 |
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 | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(48): Show |
54 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2200-980dupA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640061 | |||||||
| chr4:147640061 | C | CTT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0036 others(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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0133 others(39): 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 | a0001c0001t0001g0130 a0001c0001t0002g0010 a0001c0001t0002g0176 others(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 | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0003g0008 others(3): 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 | 8 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0173 others(5): 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 | a0001c0001t0001g0062 a0004c0004t0001g0021 a0004c0004t0001g0048 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0145 a0005c0006t0001g0018 others(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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
109 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.2200-1009T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640091 | |||||||
| chr4:147640092 | A | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
113 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2200-1010T>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640092 | |||||||
| chr4:147640179 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.2200-1255C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640337 | |||||||
| chr4:147640589 | T | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2200-1507A>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147640589 | |||||||
| chr4:147640593 | C | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0164 a0001c0001t0004g0166 others(1): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0029 |
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 | a0001c0001t0002g0170 a0001c0001t0002g0177 |
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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0003c0003t0001g0016 a0003c0003t0001g0023 a0003c0003t0001g0037 |
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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0047 | 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0082 |
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 | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.2199+258dupG | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 10/11 | chr4 | 147642528 | |||||||
| chr4:147642716 | A | G | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | a0001c0001t0007g0128 | 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 | a0001c0001t0001g0015 | 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 | 66 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(63): 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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
118 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.2046-1434delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147644373 | |||||||
| chr4:147644539 | T | TA | 82 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0025 others(79): 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0022 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): 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 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0097 others(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 | a0001c0005t0001g0058 | 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 | a0001c0001t0001g0119 | 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 | 51 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0030 others(48): 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 | a0001c0001t0001g0022 a0001c0005t0001g0057 a0001c0005t0001g0058 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0119 | 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2046-4190C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647130 | |||||||
| chr4:147647618 | G | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2046-4678C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647618 | |||||||
| chr4:147647988 | CG | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
119 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2046-5049delC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147647988 | |||||||
| chr4:147648163 | C | A | 1 | a0001c0001t0001g0060 | 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0170 a0001c0001t0002g0177 a0001c0001t0002g0178 |
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 | a0004c0004t0001g0021 a0004c0004t0001g0048 a0004c0004t0001g0049 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0002g0188 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0173 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0007g0128 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0120 | 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | a0001c0005t0001g0080 | 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 | a0001c0001t0001g0093 | 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
127 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(124): 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0006c0008t0005g0055 a0006c0008t0005g0081 |
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 | 5 | a0001c0001t0001g0129 a0001c0001t0003g0008 a0001c0001t0003g0156 others(2): 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | 2 | a0003c0003t0001g0001 a0003c0003t0001g0042 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0005t0001g0114 | 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 | a0001c0001t0002g0181 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 35 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0035 others(32): 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 | a0001c0001t0001g0059 a0001c0001t0006g0090 |
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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | 27 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0100 others(24): 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 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0013t0001g0132 |
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 | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0097 others(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 | 53 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0001t0001g0143 others(50): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0002g0178 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0010t0001g0043 |
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 | 59 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0083 others(56): 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 | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(64): 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 | a0001c0001t0001g0153 | 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2045+300C>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 9/11 | chr4 | 147653552 | |||||||
| chr4:147653810 | C | CA | 5 | a0001c0001t0001g0130 a0001c0001t0003g0008 a0001c0001t0003g0156 others(2): 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0028 | 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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1331-1253T>C | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147655819 | |||||||
| chr4:147655856 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0004c0004t0001g0021 | 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 | a0002c0002t0002g0197 | 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 | a0007c0011t0001g0122 | 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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0060 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
76 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1330+1020dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 8/11 | chr4 | 147656771 | |||||||
| chr4:147656771 | CA | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0025 | 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 | a0001c0005t0001g0115 | 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 | a0003c0003t0001g0016 a0003c0003t0001g0023 a0003c0003t0001g0037 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0040 | 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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0089 | 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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
106 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(103): 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 | a0001c0001t0001g0123 | 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 | 10 | a0003c0003t0001g0001 a0003c0003t0001g0016 a0003c0003t0001g0017 others(7): 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0083 | 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 | 27 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0074 others(24): 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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
107 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(104): 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 | a0003c0003t0001g0016 a0003c0003t0001g0023 a0003c0003t0001g0037 |
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 | |||||||
| chr4:147659573 | TC | T | 41 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(38): 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 | a0001c0001t0002g0173 a0001c0001t0002g0183 a0001c0001t0002g0191 |
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 | a0001c0001t0002g0173 a0001c0001t0002g0183 a0001c0001t0002g0191 |
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 | 41 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(38): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): 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 | a0001c0001t0002g0173 a0001c0001t0002g0183 a0001c0001t0002g0191 |
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 | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
114 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(111): 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 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0035 others(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 | a0001c0001t0002g0173 a0001c0001t0002g0183 a0001c0001t0002g0191 |
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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | 14 | a0001c0001t0004g0009 a0001c0001t0004g0164 a0001c0001t0004g0166 others(11): 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0151 | 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | 3 | a0001c0001t0003g0008 a0001c0001t0003g0157 a0009c0014t0003g0155 |
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 | a0002c0002t0002g0206 | 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 | a0001c0001t0006g0090 | 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 | a0001c0001t0001g0015 | 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
81 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.954-224delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147661261 | |||||||
| chr4:147661345 | T | C | 2 | a0006c0008t0005g0055 a0006c0008t0005g0081 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | 25 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0060 others(22): 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 | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
111 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(108): 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 | 43 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0088 others(40): 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 | a0001c0001t0001g0086 a0001c0001t0001g0162 a0001c0001t0002g0169 others(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 | 43 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(40): 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
119 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.954-1102C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662140 | |||||||
| chr4:147662157 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.954-1119A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147662157 | |||||||
| chr4:147662408 | G | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0087 | 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 | a0001c0005t0001g0058 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0003c0003t0001g0016 a0003c0003t0001g0037 |
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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0088 others(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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0002g0176 a0001c0001t0002g0185 |
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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0089 | 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 | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
179 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.953+3414dupT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665124 | |||||||
| chr4:147665124 | C | CAA | 10 | a0001c0001t0001g0038 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0184 | 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 | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0002g0167 | 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 | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.953+2692G>A | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 6/11 | chr4 | 147665847 | |||||||
| chr4:147666032 | T | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0124 others(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 | 68 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0112 others(65): 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 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0028 others(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 | a0002c0002t0002g0203 | 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 | a0004c0004t0001g0021 | 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 | a0001c0001t0001g0108 | 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 | 14 | a0002c0002t0002g0013 a0002c0002t0002g0194 a0002c0002t0002g0195 others(11): 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 | a0001c0001t0001g0041 | 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): 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 | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
190 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(187): 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 | a0001c0001t0001g0134 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0097 others(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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0045 a0001c0001t0001g0100 |
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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
144 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.847-592delC | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147669236 | |||||||
| chr4:147669237 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0101 | 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0002g0183 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
218 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(215): 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 | a0001c0001t0002g0184 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.846+242C>T | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 5/11 | chr4 | 147670399 | |||||||
| chr4:147670618 | G | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0002g0185 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0119 | 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 8 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0173 others(5): 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.743+505C>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 4/11 | chr4 | 147672454 | |||||||
| chr4:147672661 | C | T | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | a0001c0001t0001g0041 | 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 | a0003c0003t0001g0023 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
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 | a0001c0001t0001g0121 | 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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0005t0001g0105 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0108 others(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 | 49 | a0001c0001t0001g0025 a0001c0001t0001g0119 a0001c0001t0001g0129 others(46): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0133 others(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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
111 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.338+2877delA | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147677445 | |||||||
| chr4:147677445 | ATT | A | 7 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0148 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.338+2184A>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 2/11 | chr4 | 147678139 | |||||||
| chr4:147678325 | TTAAC | T | 4 | a0001c0001t0003g0008 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): 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 | 24 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(21): 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0169 | 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0119 | 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 | a0001c0007t0001g0032 | 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 | 44 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(41): 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0119 | 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 | a0002c0002t0002g0206 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0013t0001g0132 |
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 | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.190-1123T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681594 | |||||||
| chr4:147681616 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(117): 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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
143 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.190-1313delT | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147681783 | |||||||
| chr4:147681797 | A | C | 1 | a0001c0001t0001g0015 | 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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): 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 | a0001c0001t0001g0030 | 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 | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.189+1398T>G | PRMT9 | ENSG00000164169.13 | transcript | ENST00000322396.7 | protein_coding | 1/11 | chr4 | 147682401 | |||||||
| chr4:147682422 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): 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 | a0001c0001t0002g0168 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | 5 | a0001c0001t0001g0027 a0001c0001t0004g0009 a0001c0001t0004g0164 others(2): 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0002g0167 others(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 | 14 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0158 others(11): 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 | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
181 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(178): 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 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0025 others(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 | 14 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0158 others(11): 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 |