Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57017 |
| ensemblid | ENSG00000088682.14 |
| hgncid | 25302 |
| symbol | COQ9 |
| name | coenzyme Q9 |
| refseq_nuc | NM_020312.4 |
| refseq_prot | NP_064708.1 |
| ensembl_nuc | ENST00000262507.11 |
| ensembl_prot | ENSP00000262507.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 57447479 |
| end | 57461270 |
| strand | + |
| ver | v1.2 |
| region | chr16:57447479-57461270 |
| region5000 | chr16:57442479-57466270 |
| regionname0 | COQ9_chr16_57447479_57461270 |
| regionname5000 | COQ9_chr16_57442479_57466270 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 318 | 393 | 87 | 66 | 184 | 14 | 40 | 146 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0002 | 0/0 | 318 | 4 | 1 | 0 | 3 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0003 | 0/0 | 318 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0004 | 0/0 | 318 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0005 | 0/0 | 318 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0006 | 0/0 | 318 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0007 | 0/0 | 318 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| a0008 | 0/0 | 318 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | MAAAA others(313): Show |
chr16 | 57442479 | 57466270 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 954 | 383 | 82 | 64 | 182 | 13 | 40 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0001c0002 | 0/0 | 954 | 9 | 5 | 1 | 2 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0001c0010 | 0/0 | 954 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0002c0003 | 0/0 | 954 | 4 | 1 | 0 | 3 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0003c0004 | 0/0 | 954 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0004c0009 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0005c0005 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0006c0008 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0007c0006 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 | ||
| a0008c0007 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | ATGGC others(949): Show |
chr16 | 57442479 | 57466270 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1630 | 347 | 60 | 61 | 179 | 11 | 35 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0002 | 0/0 | 1630 | 24 | 17 | 2 | 0 | 2 | 3 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0003 | 0/0 | 1630 | 5 | 5 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0004 | 1/0 | 1630 | 2 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0005 | 0/0 | 1630 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0006 | 0/0 | 1630 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0007 | 0/0 | 1630 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0001t0008 | 0/0 | 1630 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0002t0002 | 0/0 | 1630 | 9 | 5 | 1 | 2 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0001c0010t0001 | 0/0 | 1630 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0002c0003t0001 | 0/0 | 1630 | 4 | 1 | 0 | 3 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0003c0004t0001 | 0/0 | 1630 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0004c0009t0001 | 0/0 | 1630 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0005c0005t0001 | 0/0 | 1630 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0006c0008t0001 | 0/0 | 1630 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0007c0006t0001 | 0/0 | 1630 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| a0008c0007t0009 | 0/0 | 1630 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | GCCGT others(1625): Show |
chr16 | 57442479 | 57466270 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 87 | 16 | 15 | 48 | 2 | 6 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0002 | 0/0 | 45 | 3 | 6 | 35 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0003 | 0/1 | 34 | 0 | 10 | 18 | 0 | 5 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0004 | 0/0 | 18 | 14 | 1 | 1 | 1 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0005 | 0/0 | 16 | 0 | 0 | 15 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 6 | 0 | 3 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0008 | 0/0 | 8 | 2 | 1 | 3 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0009 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0006 | 0/0 | 11 | 8 | 1 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0003g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0004g0002 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0002t0002g0010 | 0/0 | 6 | 2 | 1 | 2 | 1 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0001c0010t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0003c0004t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0004c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0005c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0006c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0007c0006t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| a0008c0007t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00609 | hp2 | a0004 | c0009 | t0001 | g0022 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01496 | hp2 | a0001 | c0010 | t0001 | g0009 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0055 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02602 | hp2 | a0006 | c0008 | t0001 | g0001 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02738 | hp2 | a0003 | c0004 | t0001 | g0032 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0061 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03490 | hp1 | a0003 | c0004 | t0001 | g0032 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03834 | hp2 | a0007 | c0006 | t0001 | g0003 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | CHB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19043 | hp2 | a0008 | c0007 | t0009 | g0053 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0010 | EUR | TSI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | GIH | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | USA | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | USA | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | LWK | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0002 | REF | REF | COQ9_chr16_57442479_57466270 | COQ9 | chr16 | 57442479 | 57466270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57452881 | T | G | 1 | a0005 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.323T>G | p.Leu108Arg | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/9 | 350/1630 | 323/957 | 108/318 | chr16 | 57452881 | |||
| chr16:57452895 | G | A | 1 | a0007 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.337G>A | p.Ala113Thr | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/9 | 364/1630 | 337/957 | 113/318 | chr16 | 57452895 | |||
| chr16:57456643 | C | T | 1 | a0004 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.518C>T | p.Ala173Val | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 4/9 | 545/1630 | 518/957 | 173/318 | chr16 | 57456643 | |||
| chr16:57456933 | A | G | 1 | a0006 | 1 | HG02602.hp2 | missense_variant&splice_region_variant | MODERATE | c.524A>G | p.Lys175Arg | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/9 | 551/1630 | 524/957 | 175/318 | chr16 | 57456933 | |||
| chr16:57458264 | C | G | 1 | a0002 | 4 | HG02976.hp1 NA18747.hp2 NA18956.hp1 others(1): Show |
missense_variant | MODERATE | c.625C>G | p.Leu209Val | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/9 | 652/1630 | 625/957 | 209/318 | chr16 | 57458264 | |||
| chr16:57459679 | C | T | 1 | a0003 | 2 | HG02738.hp2 HG03490.hp1 |
missense_variant | MODERATE | c.826C>T | p.Arg276Trp | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 7/9 | 853/1630 | 826/957 | 276/318 | chr16 | 57459679 | |||
| chr16:57459717 | G | C | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.864G>C | p.Lys288Asn | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 7/9 | 891/1630 | 864/957 | 288/318 | chr16 | 57459717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57447523 | A | G | 1 | a0001c0010 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.18A>G | p.Val6Val | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/9 | 45/1630 | 18/957 | 6/318 | chr16 | 57447523 | |||
| chr16:57451068 | G | A | 1 | a0001c0002 | 9 | HG01243.hp1 HG02056.hp2 HG02630.hp2 others(6): Show |
synonymous_variant | LOW | c.102G>A | p.Pro34Pro | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/9 | 129/1630 | 102/957 | 34/318 | chr16 | 57451068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57460724 | C | T | 1 | a0001c0001t0005 | 2 | HG03669.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*100C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 100 | chr16 | 57460724 | ||||||
| chr16:57461035 | C | T | 1 | a0008c0007t0009 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 411 | chr16 | 57461035 | ||||||
| chr16:57461080 | C | A | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0002t0002 |
38 | HG01069.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*456C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 456 | chr16 | 57461080 | ||||||
| chr16:57461100 | G | C | 1 | a0001c0001t0006 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 476 | chr16 | 57461100 | ||||||
| chr16:57461114 | T | C | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
401 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(398): Show |
3_prime_UTR_variant | MODIFIER | c.*490T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 490 | chr16 | 57461114 | ||||||
| chr16:57461124 | C | G | 1 | a0001c0001t0008 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 500 | chr16 | 57461124 | ||||||
| chr16:57461162 | C | T | 1 | a0001c0001t0007 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 538 | chr16 | 57461162 | ||||||
| chr16:57461169 | G | T | 1 | a0001c0001t0003 | 5 | HG02717.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*545G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 9/9 | 545 | chr16 | 57461169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57447657 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.73+79G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57447657 | |||||||
| chr16:57447729 | G | C | 1 | a0001c0001t0002g0021 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.73+151G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57447729 | |||||||
| chr16:57447758 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.73+180T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57447758 | |||||||
| chr16:57447874 | G | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.73+296G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57447874 | |||||||
| chr16:57447937 | A | C | 1 | a0002c0003t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.73+359A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57447937 | |||||||
| chr16:57448083 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.73+505T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448083 | |||||||
| chr16:57448255 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.73+677C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448255 | |||||||
| chr16:57448285 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73+707T>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448285 | |||||||
| chr16:57448344 | C | CT | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0021 |
6 | HG00438.hp2 HG03486.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+780dupT | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 57448344 | ||||||
| chr16:57448344 | CT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0022 others(8): Show |
29 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.73+780delT | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 57448344 | ||||||
| chr16:57448361 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.73+783G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448361 | |||||||
| chr16:57448368 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG02257.hp1 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+790G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448368 | |||||||
| chr16:57448454 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.73+876C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448454 | |||||||
| chr16:57448644 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.73+1066C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448644 | |||||||
| chr16:57448745 | A | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0033 others(1): Show |
8 | HG00639.hp1 HG01192.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.73+1167A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448745 | |||||||
| chr16:57448892 | C | A | 1 | a0002c0003t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.73+1314C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448892 | |||||||
| chr16:57448949 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0025 |
5 | HG01123.hp2 HG01175.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+1371A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57448949 | |||||||
| chr16:57449004 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0054 |
4 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.73+1426T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449004 | |||||||
| chr16:57449008 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.73+1430A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449008 | |||||||
| chr16:57449038 | C | A | 1 | a0001c0001t0001g0016 | 3 | HG02559.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.73+1460C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449038 | |||||||
| chr16:57449120 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
166 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.73+1542C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449120 | |||||||
| chr16:57449132 | A | C | 1 | a0002c0003t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.73+1554A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449132 | |||||||
| chr16:57449269 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.73+1691G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449269 | |||||||
| chr16:57449278 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(2): Show |
16 | HG00642.hp2 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.73+1700T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449278 | |||||||
| chr16:57449283 | C | T | 1 | a0008c0007t0009g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73+1705C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449283 | |||||||
| chr16:57449323 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.74-1717A>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449323 | |||||||
| chr16:57449463 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.74-1577C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449463 | |||||||
| chr16:57449643 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.74-1397A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449643 | |||||||
| chr16:57449650 | T | C | 1 | a0005c0005t0001g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.74-1390T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449650 | |||||||
| chr16:57449682 | G | GCTTTACT others(4): Show |
1 | a0002c0003t0001g0090 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.74-1356_74-1346dup others(11): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 57449682 | ||||||
| chr16:57449763 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(5): Show |
31 | HG00438.hp1 HG01358.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.74-1277A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449763 | |||||||
| chr16:57449772 | A | G | 1 | a0002c0003t0001g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.74-1268A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449772 | |||||||
| chr16:57449955 | G | A | 4 | a0001c0002t0002g0010 a0001c0002t0002g0048 a0001c0002t0002g0056 others(1): Show |
9 | HG01243.hp1 HG02056.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.74-1085G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57449955 | |||||||
| chr16:57450052 | G | A | 4 | a0002c0003t0001g0058 a0002c0003t0001g0059 a0002c0003t0001g0061 others(1): Show |
4 | HG02976.hp1 NA18747.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-988G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57450052 | |||||||
| chr16:57450135 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.74-905C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57450135 | |||||||
| chr16:57450232 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.74-808G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57450232 | |||||||
| chr16:57450412 | C | CA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(28): Show |
80 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.74-610dupA | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 57450412 | ||||||
| chr16:57450412 | CA | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(20): Show |
71 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.74-610delA | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 57450412 | ||||||
| chr16:57451005 | G | A | 5 | a0001c0001t0003g0012 a0001c0002t0002g0010 a0001c0002t0002g0048 others(2): Show |
14 | HG01243.hp1 HG02056.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.74-35G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 1/8 | chr16 | 57451005 | |||||||
| chr16:57451310 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.242+102C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451310 | |||||||
| chr16:57451320 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.242+112G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451320 | |||||||
| chr16:57451458 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 |
4 | HG02257.hp1 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+250C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451458 | |||||||
| chr16:57451637 | C | G | 1 | a0001c0001t0002g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.242+429C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451637 | |||||||
| chr16:57451678 | T | C | 1 | a0005c0005t0001g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.242+470T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451678 | |||||||
| chr16:57451722 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.242+514A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57451722 | |||||||
| chr16:57452053 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.243-748T>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452053 | |||||||
| chr16:57452099 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(5): Show |
31 | HG00438.hp1 HG01358.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.243-702G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452099 | |||||||
| chr16:57452135 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
32 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.243-666C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452135 | |||||||
| chr16:57452162 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0050 |
3 | HG03491.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.243-639C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452162 | |||||||
| chr16:57452241 | T | A | 1 | a0001c0001t0002g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.243-560T>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452241 | |||||||
| chr16:57452368 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.243-433G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452368 | |||||||
| chr16:57452514 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.243-287C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452514 | |||||||
| chr16:57452529 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243-272C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452529 | |||||||
| chr16:57452546 | G | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.243-255G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452546 | |||||||
| chr16:57452639 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0108 |
2 | NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.243-162C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452639 | |||||||
| chr16:57452671 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0026 a0001c0001t0002g0027 others(2): Show |
18 | HG01069.hp1 HG01109.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.243-130T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452671 | |||||||
| chr16:57452701 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
166 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.243-100C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 2/8 | chr16 | 57452701 | |||||||
| chr16:57453079 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0033 others(1): Show |
8 | HG00639.hp1 HG01192.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+143A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453079 | |||||||
| chr16:57453110 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0086 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.378+174T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453110 | |||||||
| chr16:57453186 | CA | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG02257.hp1 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+254delA | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57453186 | ||||||
| chr16:57453210 | CTAAGATG others(10): Show |
C | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.378+280_378+296del others(17): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57453210 | ||||||
| chr16:57453583 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.378+647C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453583 | |||||||
| chr16:57453787 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.378+851T>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453787 | |||||||
| chr16:57453806 | A | C | 1 | a0001c0001t0001g0042 | 2 | HG02027.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.378+870A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453806 | |||||||
| chr16:57453934 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.378+998A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453934 | |||||||
| chr16:57453935 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.378+999G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57453935 | |||||||
| chr16:57454075 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.378+1139C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454075 | |||||||
| chr16:57454297 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.378+1361A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454297 | |||||||
| chr16:57454341 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.378+1405A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454341 | |||||||
| chr16:57454374 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0086 |
3 | HG02896.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.378+1438G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454374 | |||||||
| chr16:57454387 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.378+1451C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454387 | |||||||
| chr16:57454524 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0065 |
4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+1588G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454524 | |||||||
| chr16:57454531 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.378+1595G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454531 | |||||||
| chr16:57454538 | G | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 |
4 | HG02257.hp1 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+1602G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454538 | |||||||
| chr16:57454622 | C | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
166 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.378+1686C>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454622 | |||||||
| chr16:57454815 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.379-1689G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454815 | |||||||
| chr16:57454822 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0075 |
8 | HG01934.hp1 HG01975.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-1682G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454822 | |||||||
| chr16:57454890 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.379-1614C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57454890 | |||||||
| chr16:57455022 | G | T | 1 | a0008c0007t0009g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-1482G>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455022 | |||||||
| chr16:57455044 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
37 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.379-1460A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455044 | |||||||
| chr16:57455188 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0092 |
3 | NA18969.hp2 NA18995.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.379-1316A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455188 | |||||||
| chr16:57455356 | C | CAT | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0054 others(4): Show |
21 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.379-1132_379-1131d others(4): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455356 | ||||||
| chr16:57455356 | C | CATAT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.379-1134_379-1131d others(6): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455356 | ||||||
| chr16:57455356 | C | CATATAT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0085 others(2): Show |
12 | HG00597.hp1 HG01496.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.379-1136_379-1131d others(8): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455356 | ||||||
| chr16:57455356 | CAT | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(18): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.379-1132_379-1131d others(4): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455356 | ||||||
| chr16:57455397 | T | TTA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(9): Show |
39 | HG00438.hp1 HG01358.hp1 HG01515.hp2 others(36): Show |
intron_variant | MODIFIER | c.379-1088_379-1087d others(4): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455397 | ||||||
| chr16:57455397 | T | TTATA | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0063 others(2): Show |
9 | HG00639.hp1 HG01192.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-1090_379-1087d others(6): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455397 | ||||||
| chr16:57455397 | T | TTATATA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0025 others(3): Show |
25 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.379-1092_379-1087d others(8): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455397 | ||||||
| chr16:57455397 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0046 |
6 | HG00558.hp1 HG00673.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1094_379-1087d others(10): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455397 | ||||||
| chr16:57455397 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0022 a0004c0009t0001g0022 |
2 | HG00609.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.379-1098_379-1087d others(14): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 57455397 | ||||||
| chr16:57455454 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.379-1050A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455454 | |||||||
| chr16:57455506 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
32 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.379-998T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455506 | |||||||
| chr16:57455511 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG02257.hp1 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-993G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455511 | |||||||
| chr16:57455626 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
166 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.379-878G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455626 | |||||||
| chr16:57455868 | A | G | 1 | a0001c0001t0003g0012 | 5 | HG02717.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-636A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455868 | |||||||
| chr16:57455871 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0022 others(5): Show |
26 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.379-633A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455871 | |||||||
| chr16:57455979 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.379-525G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57455979 | |||||||
| chr16:57456081 | CAA | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0054 |
4 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-422_379-421del others(2): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57456081 | |||||||
| chr16:57456120 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.379-384T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57456120 | |||||||
| chr16:57456231 | G | C | 1 | a0001c0001t0001g0019 | 3 | HG01106.hp1 HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.379-273G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 3/8 | chr16 | 57456231 | |||||||
| chr16:57456774 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.521+128G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 4/8 | chr16 | 57456774 | |||||||
| chr16:57456809 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.522-122G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 4/8 | chr16 | 57456809 | |||||||
| chr16:57456870 | G | A | 1 | a0001c0001t0001g0020 | 3 | NA18945.hp1 NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.522-61G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 4/8 | chr16 | 57456870 | |||||||
| chr16:57456900 | G | C | 1 | a0001c0001t0001g0041 | 2 | NA19005.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.522-31G>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 4/8 | chr16 | 57456900 | |||||||
| chr16:57457414 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.606+399A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457414 | |||||||
| chr16:57457559 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.606+544C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457559 | |||||||
| chr16:57457613 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.606+598A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457613 | |||||||
| chr16:57457619 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.606+604G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457619 | |||||||
| chr16:57457680 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.607-566C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457680 | |||||||
| chr16:57457939 | CTG | C | 1 | a0001c0001t0001g0013 | 5 | HG00438.hp1 NA19003.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-306_607-305del others(2): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57457939 | |||||||
| chr16:57457944 | G | GT | 6 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0026 others(3): Show |
20 | HG01069.hp1 HG01109.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.607-301dupT | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 57457944 | ||||||
| chr16:57458060 | C | G | 1 | a0001c0001t0003g0012 | 5 | HG02717.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-186C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57458060 | |||||||
| chr16:57458084 | C | T | 3 | a0001c0002t0002g0010 a0001c0002t0002g0048 a0001c0002t0002g0056 |
8 | HG01243.hp1 HG02056.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-162C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57458084 | |||||||
| chr16:57458107 | C | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0025 |
6 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-139C>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57458107 | |||||||
| chr16:57458162 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.607-84T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57458162 | |||||||
| chr16:57458230 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.607-16G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 5/8 | chr16 | 57458230 | |||||||
| chr16:57458492 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.711+142C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458492 | |||||||
| chr16:57458494 | T | C | 1 | a0005c0005t0001g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.711+144T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458494 | |||||||
| chr16:57458611 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.711+261T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458611 | |||||||
| chr16:57458615 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | NA18940.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.711+265C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458615 | |||||||
| chr16:57458616 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.711+266G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458616 | |||||||
| chr16:57458756 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.711+406T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458756 | |||||||
| chr16:57458770 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.711+420G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458770 | |||||||
| chr16:57458994 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.712-571C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57458994 | |||||||
| chr16:57459259 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.712-306A>G | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57459259 | |||||||
| chr16:57459289 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.712-276C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57459289 | |||||||
| chr16:57459371 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.712-194G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57459371 | |||||||
| chr16:57459385 | A | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
4 | HG02451.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-180A>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57459385 | |||||||
| chr16:57459471 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.712-94T>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 6/8 | chr16 | 57459471 | |||||||
| chr16:57459890 | TCATTTG | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.868-154_868-149del others(6): Show |
COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 57459890 | ||||||
| chr16:57460019 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.868-32G>A | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 7/8 | chr16 | 57460019 | |||||||
| chr16:57460024 | A | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0080 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.868-27A>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 7/8 | chr16 | 57460024 | |||||||
| chr16:57460117 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
6 | HG01123.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+13C>T | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 8/8 | chr16 | 57460117 | |||||||
| chr16:57460266 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.921+162T>C | COQ9 | ENSG00000088682.14 | transcript | ENST00000262507.11 | protein_coding | 8/8 | chr16 | 57460266 |