Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79934 |
| ensemblid | ENSG00000123815.13 |
| hgncid | 19041 |
| symbol | COQ8B |
| name | coenzyme Q8B |
| refseq_nuc | NM_024876.4 |
| refseq_prot | NP_079152.3 |
| ensembl_nuc | ENST00000324464.8 |
| ensembl_prot | ENSP00000315118.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 40691530 |
| end | 40716886 |
| strand | - |
| ver | v1.2 |
| region | chr19:40691530-40716886 |
| region5000 | chr19:40686530-40721886 |
| regionname0 | COQ8B_chr19_40691530_40716886 |
| regionname5000 | COQ8B_chr19_40686530_40721886 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 544 | 218 | 62 | 29 | 97 | 7 | 21 | 74 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0002 | 0/0 | 544 | 177 | 31 | 42 | 78 | 8 | 18 | 60 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0003 | 0/0 | 544 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0004 | 0/0 | 544 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0005 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0006 | 0/0 | 544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0007 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0008 | 0/0 | 544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0009 | 0/0 | 79 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(74): Show |
chr19 | 40686530 | 40721886 |
| a0010 | 0/0 | 544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0011 | 0/0 | 544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0012 | 0/0 | 544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| a0013 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | MWLKV others(539): Show |
chr19 | 40686530 | 40721886 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 1632 | 94 | 37 | 2 | 49 | 2 | 3 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0003 | 0/1 | 1632 | 78 | 7 | 14 | 37 | 2 | 17 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0004 | 0/0 | 1632 | 29 | 14 | 11 | 1 | 2 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0005 | 0/0 | 1632 | 8 | 0 | 0 | 8 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0007 | 0/0 | 1632 | 4 | 1 | 2 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0012 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0014 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0018 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0019 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0001c0020 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0001 | 0/0 | 1632 | 165 | 21 | 41 | 77 | 8 | 18 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0006 | 0/0 | 1632 | 5 | 5 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0008 | 0/0 | 1632 | 4 | 4 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0023 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0024 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0002c0025 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0003c0010 | 0/0 | 1632 | 3 | 0 | 2 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0004c0009 | 0/0 | 1632 | 3 | 0 | 0 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0005c0016 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0006c0015 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0007c0011 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0008c0021 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0009c0026 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0010c0027 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0011c0013 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0012c0022 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 | ||
| a0013c0017 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | ATGTG others(1627): Show |
chr19 | 40686530 | 40721886 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 2443 | 89 | 32 | 2 | 49 | 2 | 3 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0002t0004 | 0/0 | 2443 | 4 | 4 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0002t0006 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0003t0001 | 0/1 | 2443 | 78 | 7 | 14 | 37 | 2 | 17 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0004t0001 | 0/0 | 2443 | 29 | 14 | 11 | 1 | 2 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0005t0001 | 0/0 | 2443 | 8 | 0 | 0 | 8 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0007t0001 | 0/0 | 2443 | 4 | 1 | 2 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0012t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0014t0001 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0018t0003 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0019t0001 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0001c0020t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0001t0001 | 0/0 | 2443 | 156 | 20 | 34 | 76 | 8 | 18 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0001t0002 | 0/0 | 2443 | 7 | 0 | 7 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0001t0004 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0001t0007 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0006t0003 | 0/0 | 2443 | 5 | 5 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0008t0001 | 0/0 | 2443 | 4 | 4 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0023t0001 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0024t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0002c0025t0001 | 0/0 | 2443 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0003c0010t0001 | 0/0 | 2443 | 3 | 0 | 2 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0004c0009t0001 | 0/0 | 2443 | 3 | 0 | 0 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0005c0016t0001 | 0/0 | 2443 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0006c0015t0001 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0007c0011t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0008c0021t0001 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0009c0026t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0010c0027t0005 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0011c0013t0001 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0012c0022t0001 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| a0013c0017t0001 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | CTCTG others(2438): Show |
chr19 | 40686530 | 40721886 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0002t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0005t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0007t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0007t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0012t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0014t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0018t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0019t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0001c0020t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 4 | 1 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0006t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0006t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0006t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0006t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0006t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0008t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0008t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0023t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0024t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0002c0025t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0003c0010t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0003c0010t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0003c0010t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0004c0009t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0004c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0005c0016t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0006c0015t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0007c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0008c0021t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0009c0026t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0010c0027t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0011c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0012c0022t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| a0013c0017t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0242 | EUR | GBR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0020 | EUR | GBR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0243 | EUR | GBR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0262 | EUR | GBR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0109 | EUR | FIN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | FIN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0335 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0076 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0289 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0258 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00639 | hp2 | a0003 | c0010 | t0001 | g0052 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0148 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00642 | hp2 | a0002 | c0001 | t0002 | g0154 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00673 | hp2 | a0001 | c0005 | t0001 | g0303 | EAS | CHS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00735 | hp1 | a0002 | c0025 | t0001 | g0051 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0119 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0249 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0016 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0267 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01070 | hp1 | a0001 | c0007 | t0001 | g0031 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0239 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01071 | hp1 | a0001 | c0007 | t0001 | g0031 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0012 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0212 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0064 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0211 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0018 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0143 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01169 | hp2 | a0002 | c0001 | t0001 | g0018 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0255 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0261 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0266 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0126 | AMR | PUR | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0264 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0129 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0146 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0213 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01257 | hp1 | a0001 | c0004 | t0001 | g0248 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0102 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01346 | hp2 | a0003 | c0010 | t0001 | g0053 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0085 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0238 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01433 | hp1 | a0002 | c0001 | t0002 | g0009 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0190 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0259 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0140 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0016 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0010 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0091 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0041 | EUR | IBS | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0165 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0099 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0141 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0103 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0178 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0280 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0191 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01952 | hp2 | a0002 | c0001 | t0002 | g0009 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0153 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0139 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0065 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01993 | hp1 | a0002 | c0001 | t0002 | g0009 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0168 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02027 | hp1 | a0002 | c0023 | t0001 | g0062 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02055 | hp1 | a0002 | c0006 | t0003 | g0152 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0098 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02148 | hp1 | a0002 | c0001 | t0002 | g0156 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0101 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | CDX | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02155 | hp2 | a0002 | c0001 | t0007 | g0132 | EAS | CDX | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02165 | hp1 | a0004 | c0009 | t0001 | g0105 | EAS | CDX | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | CDX | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0006 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0155 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0087 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02293 | hp2 | a0005 | c0016 | t0001 | g0196 | AMR | PEL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | KHV | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0223 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02615 | hp1 | a0002 | c0006 | t0003 | g0135 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0347 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0257 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02630 | hp1 | a0002 | c0006 | t0003 | g0122 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0254 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02647 | hp1 | a0002 | c0001 | t0004 | g0121 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0020 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02717 | hp1 | a0002 | c0006 | t0003 | g0230 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02723 | hp1 | a0002 | c0008 | t0001 | g0278 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0256 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02735 | hp1 | a0006 | c0015 | t0001 | g0187 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0110 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0071 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0342 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0240 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02895 | hp2 | a0002 | c0006 | t0003 | g0158 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02896 | hp1 | a0002 | c0008 | t0001 | g0030 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0260 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02897 | hp2 | a0002 | c0008 | t0001 | g0030 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0127 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0343 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02970 | hp1 | a0001 | c0012 | t0001 | g0060 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0096 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02976 | hp2 | a0007 | c0011 | t0001 | g0166 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03017 | hp1 | a0008 | c0021 | t0001 | g0199 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0210 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03098 | hp2 | a0002 | c0024 | t0001 | g0350 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0344 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03195 | hp2 | a0001 | c0018 | t0003 | g0227 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0055 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0348 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0277 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0235 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0330 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03453 | hp1 | a0002 | c0008 | t0001 | g0228 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03453 | hp2 | a0009 | c0026 | t0001 | g0162 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0251 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03516 | hp1 | a0001 | c0020 | t0001 | g0232 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | ESN | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0006 | AFR | GWD | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0345 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0095 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0295 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0186 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03669 | hp1 | a0010 | c0027 | t0005 | g0038 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0265 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0083 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0294 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0147 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0216 | SAS | PJL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0066 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0010 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0117 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0039 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0224 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0124 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0149 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0320 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0177 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0183 | SAS | BEB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0189 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0107 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0007 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0063 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0194 | SAS | STU | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0245 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | CHB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | CHB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | CHB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0093 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0286 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0290 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18947 | hp2 | a0001 | c0005 | t0001 | g0046 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18952 | hp2 | a0001 | c0014 | t0001 | g0192 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0244 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0285 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0161 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18966 | hp2 | a0011 | c0013 | t0001 | g0174 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18969 | hp1 | a0001 | c0005 | t0001 | g0078 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18978 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18998 | hp1 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0067 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19004 | hp1 | a0001 | c0005 | t0001 | g0079 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0292 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0291 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19011 | hp1 | a0001 | c0005 | t0001 | g0081 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19012 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19012 | hp2 | a0004 | c0009 | t0001 | g0019 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0094 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0263 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19043 | hp1 | a0002 | c0001 | t0001 | g0349 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19058 | hp1 | a0001 | c0005 | t0001 | g0047 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19065 | hp1 | a0004 | c0009 | t0001 | g0019 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0287 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0049 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19067 | hp2 | a0012 | c0022 | t0001 | g0157 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0288 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0279 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19089 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19090 | hp1 | a0001 | c0019 | t0001 | g0331 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA19240 | hp2 | a0002 | c0001 | t0001 | g0108 | AFR | YRI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0006 | AFR | ASW | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | ASW | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0215 | EUR | TSI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20752 | hp2 | a0003 | c0010 | t0001 | g0044 | EUR | TSI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0142 | EUR | TSI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0236 | EUR | TSI | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0195 | SAS | GIH | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | GIH | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0284 | AMR | CLM | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0128 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0237 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0144 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | MSL | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0247 | AFR | USA | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| HG06807 | hp2 | a0001 | c0007 | t0001 | g0241 | AFR | USA | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0086 | AFR | USA | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0346 | AFR | USA | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| NA21309 | hp2 | a0013 | c0017 | t0001 | g0221 | AFR | LWK | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0181 | REF | REF | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0169 | REF | REF | COQ8B_chr19_40686530_40721886 | COQ8B | chr19 | 40686530 | 40721886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:40692310 | G | A | 1 | a0006 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1360C>T | p.Pro454Ser | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1663/2443 | 1360/1635 | 454/544 | chr19 | 40692310 | |||
| chr19:40692361 | C | T | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1309G>A | p.Ala437Thr | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1612/2443 | 1309/1635 | 437/544 | chr19 | 40692361 | |||
| chr19:40700144 | G | A | 1 | a0005 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1066C>T | p.Arg356Trp | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/15 | 1369/2443 | 1066/1635 | 356/544 | chr19 | 40700144 | |||
| chr19:40702667 | C | G | 1 | a0011 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.826G>C | p.Ala276Pro | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/15 | 1129/2443 | 826/1635 | 276/544 | chr19 | 40702667 | |||
| chr19:40703616 | C | T | 1 | a0012 | 1 | NA19067.hp2 | missense_variant | MODERATE | c.724G>A | p.Gly242Ser | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/15 | 1027/2443 | 724/1635 | 242/544 | chr19 | 40703616 | |||
| chr19:40703800 | T | C | 1 | a0008 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.632A>G | p.Glu211Gly | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 8/15 | 935/2443 | 632/1635 | 211/544 | chr19 | 40703800 | |||
| chr19:40705151 | T | C | 5 | a0002 a0003 a0004 others(2): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
missense_variant | MODERATE | c.521A>G | p.His174Arg | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/15 | 824/2443 | 521/1635 | 174/544 | chr19 | 40705151 | |||
| chr19:40705171 | G | T | 1 | a0004 | 3 | HG02165.hp1 NA19012.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.501C>A | p.Phe167Leu | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/15 | 804/2443 | 501/1635 | 167/544 | chr19 | 40705171 | |||
| chr19:40714118 | G | A | 1 | a0009 | 1 | HG03453.hp2 | stop_gained | HIGH | c.238C>T | p.Arg80* | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/15 | 541/2443 | 238/1635 | 80/544 | chr19 | 40714118 | |||
| chr19:40714124 | G | A | 1 | a0003 | 3 | HG00639.hp2 HG01346.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.232C>T | p.Arg78Cys | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/15 | 535/2443 | 232/1635 | 78/544 | chr19 | 40714124 | |||
| chr19:40714384 | C | A | 1 | a0010 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.116G>T | p.Gly39Val | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 3/15 | 419/2443 | 116/1635 | 39/544 | chr19 | 40714384 | |||
| chr19:40714613 | C | T | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.20G>A | p.Gly7Asp | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 2/15 | 323/2443 | 20/1635 | 7/544 | chr19 | 40714613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:40692092 | G | A | 2 | a0001c0005 a0001c0014 |
9 | HG00609.hp1 HG00673.hp2 NA18947.hp2 others(6): Show |
synonymous_variant | LOW | c.1578C>T | p.Asp526Asp | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1881/2443 | 1578/1635 | 526/544 | chr19 | 40692092 | |||
| chr19:40692251 | C | T | 2 | a0001c0019 a0001c0020 |
2 | HG03516.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.1419G>A | p.Leu473Leu | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1722/2443 | 1419/1635 | 473/544 | chr19 | 40692251 | |||
| chr19:40692305 | A | G | 2 | a0001c0018 a0002c0006 |
6 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
synonymous_variant | LOW | c.1365T>C | p.Tyr455Tyr | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1668/2443 | 1365/1635 | 455/544 | chr19 | 40692305 | |||
| chr19:40692323 | G | A | 1 | a0001c0020 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1347C>T | p.Phe449Phe | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 1650/2443 | 1347/1635 | 449/544 | chr19 | 40692323 | |||
| chr19:40695992 | G | A | 1 | a0002c0024 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1206C>T | p.Ile402Ile | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/15 | 1509/2443 | 1206/1635 | 402/544 | chr19 | 40695992 | |||
| chr19:40703572 | C | T | 10 | a0001c0003 a0001c0007 a0001c0014 others(7): Show |
89 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(86): Show |
synonymous_variant | LOW | c.768G>A | p.Ala256Ala | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/15 | 1071/2443 | 768/1635 | 256/544 | chr19 | 40703572 | |||
| chr19:40703784 | G | A | 2 | a0002c0025 a0003c0010 |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
synonymous_variant | LOW | c.648C>T | p.Ala216Ala | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 8/15 | 951/2443 | 648/1635 | 216/544 | chr19 | 40703784 | |||
| chr19:40705138 | C | T | 1 | a0001c0012 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.534G>A | p.Arg178Arg | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/15 | 837/2443 | 534/1635 | 178/544 | chr19 | 40705138 | |||
| chr19:40714293 | C | T | 1 | a0002c0008 | 4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.207G>A | p.Lys69Lys | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 3/15 | 510/2443 | 207/1635 | 69/544 | chr19 | 40714293 | |||
| chr19:40714624 | C | T | 2 | a0001c0004 a0001c0007 |
33 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(30): Show |
synonymous_variant | LOW | c.9G>A | p.Leu3Leu | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 2/15 | 312/2443 | 9/1635 | 3/544 | chr19 | 40714624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:40691591 | C | A | 1 | a0002c0001t0002 | 7 | HG00642.hp2 HG01433.hp1 HG01952.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*444G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 444 | chr19 | 40691591 | ||||||
| chr19:40691618 | C | G | 1 | a0001c0002t0001 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 417 | chr19 | 40691618 | ||||||
| chr19:40691861 | G | A | 1 | a0001c0002t0006 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 174 | chr19 | 40691861 | ||||||
| chr19:40691895 | G | A | 1 | a0002c0001t0007 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 140 | chr19 | 40691895 | ||||||
| chr19:40691898 | C | T | 2 | a0001c0018t0003 a0002c0006t0003 |
6 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*137G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 137 | chr19 | 40691898 | ||||||
| chr19:40692025 | A | G | 2 | a0001c0002t0004 a0002c0001t0004 |
5 | HG02486.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 15/15 | 10 | chr19 | 40692025 | ||||||
| chr19:40716618 | C | T | 1 | a0010c0027t0005 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/15 | 1986 | chr19 | 40716618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:40692448 | G | A | 1 | a0001c0003t0001g0330 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1297-75C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692448 | |||||||
| chr19:40692552 | G | A | 2 | a0001c0007t0001g0031 a0001c0007t0001g0241 |
3 | HG01070.hp1 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1297-179C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692552 | |||||||
| chr19:40692562 | C | T | 1 | a0002c0001t0001g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1297-189G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692562 | |||||||
| chr19:40692577 | T | C | 225 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(222): Show |
247 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.1297-204A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692577 | |||||||
| chr19:40692662 | C | T | 1 | a0001c0003t0001g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1296+289G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692662 | |||||||
| chr19:40692702 | A | G | 1 | a0002c0025t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1296+249T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692702 | |||||||
| chr19:40692730 | C | T | 5 | a0001c0002t0001g0276 a0001c0004t0001g0240 a0001c0004t0001g0258 others(2): Show |
5 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+221G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 14/14 | chr19 | 40692730 | |||||||
| chr19:40693047 | C | T | 5 | a0001c0002t0004g0237 a0001c0002t0004g0342 a0001c0002t0004g0343 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1210-10G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693047 | |||||||
| chr19:40693074 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1210-37C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693074 | |||||||
| chr19:40693085 | G | A | 1 | a0001c0003t0001g0193 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1210-48C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693085 | |||||||
| chr19:40693316 | A | G | 1 | a0001c0002t0001g0341 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1210-279T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693316 | |||||||
| chr19:40693357 | G | A | 1 | a0001c0002t0001g0316 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1210-320C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693357 | |||||||
| chr19:40693438 | G | C | 2 | a0002c0025t0001g0051 a0003c0010t0001g0052 |
2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1210-401C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693438 | |||||||
| chr19:40693452 | C | T | 1 | a0013c0017t0001g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1210-415G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693452 | |||||||
| chr19:40693466 | C | T | 1 | a0001c0002t0001g0341 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1210-429G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693466 | |||||||
| chr19:40693495 | A | C | 1 | a0001c0002t0001g0077 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1210-458T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693495 | |||||||
| chr19:40693525 | G | A | 1 | a0001c0003t0001g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1210-488C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693525 | |||||||
| chr19:40693629 | G | A | 1 | a0002c0001t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1210-592C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693629 | |||||||
| chr19:40693670 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1210-633A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693670 | |||||||
| chr19:40693682 | A | G | 2 | a0001c0002t0001g0276 a0002c0024t0001g0350 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1210-645T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693682 | |||||||
| chr19:40693757 | C | T | 2 | a0001c0005t0001g0079 a0002c0001t0001g0282 |
2 | NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1210-720G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693757 | |||||||
| chr19:40693813 | T | C | 38 | a0001c0002t0004g0342 a0001c0003t0001g0070 a0001c0003t0001g0184 others(35): Show |
41 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1210-776A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693813 | |||||||
| chr19:40693872 | C | CT | 56 | a0001c0002t0001g0035 a0001c0002t0001g0058 a0001c0002t0001g0269 others(53): Show |
63 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210-836_1210-835i others(3): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693872 | |||||||
| chr19:40693873 | G | T | 34 | a0001c0002t0001g0059 a0001c0002t0001g0268 a0001c0002t0001g0272 others(31): Show |
34 | HG00673.hp2 HG01891.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.1210-836C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693873 | |||||||
| chr19:40693894 | G | A | 1 | a0001c0004t0001g0242 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1210-857C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693894 | |||||||
| chr19:40693914 | A | G | 1 | a0013c0017t0001g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1210-877T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40693914 | |||||||
| chr19:40694082 | T | C | 1 | a0001c0003t0001g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1210-1045A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694082 | |||||||
| chr19:40694087 | C | G | 2 | a0002c0008t0001g0030 a0002c0024t0001g0350 |
3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1210-1050G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694087 | |||||||
| chr19:40694177 | C | A | 1 | a0002c0001t0001g0021 | 2 | HG00408.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1210-1140G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694177 | |||||||
| chr19:40694329 | T | C | 9 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0001g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1210-1292A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694329 | |||||||
| chr19:40694484 | C | A | 1 | a0002c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1210-1447G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694484 | |||||||
| chr19:40694493 | C | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1210-1456G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694493 | |||||||
| chr19:40694508 | C | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1210-1471G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694508 | |||||||
| chr19:40694510 | T | C | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1210-1473A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694510 | |||||||
| chr19:40694511 | C | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1210-1474G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694511 | |||||||
| chr19:40694522 | T | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1467A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694522 | |||||||
| chr19:40694532 | T | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1457A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694532 | |||||||
| chr19:40694536 | A | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1453T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694536 | |||||||
| chr19:40694537 | C | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1452G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694537 | |||||||
| chr19:40694539 | A | C | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1450T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694539 | |||||||
| chr19:40694541 | C | T | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1448G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694541 | |||||||
| chr19:40694542 | A | T | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1447T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694542 | |||||||
| chr19:40694543 | G | C | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1446C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694543 | |||||||
| chr19:40694545 | G | T | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1444C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694545 | |||||||
| chr19:40694549 | T | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1440A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694549 | |||||||
| chr19:40694551 | C | A | 3 | a0001c0002t0001g0077 a0001c0002t0001g0080 a0002c0001t0001g0108 |
3 | HG02559.hp2 HG04204.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1209+1438G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694551 | |||||||
| chr19:40694551 | C | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1438G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694551 | |||||||
| chr19:40694552 | C | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1437G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694552 | |||||||
| chr19:40694556 | A | C | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1433T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694556 | |||||||
| chr19:40694557 | C | T | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1432G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694557 | |||||||
| chr19:40694558 | G | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1431C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694558 | |||||||
| chr19:40694566 | C | A | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1423G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694566 | |||||||
| chr19:40694567 | T | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1422A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694567 | |||||||
| chr19:40694587 | T | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1402A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694587 | |||||||
| chr19:40694588 | C | CTCATGGA others(5): Show |
1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1400_1209+140 others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694588 | |||||||
| chr19:40694591 | A | G | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1398T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694591 | |||||||
| chr19:40694595 | T | C | 1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1209+1394A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694595 | |||||||
| chr19:40694606 | A | G | 222 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(219): Show |
244 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.1209+1383T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694606 | |||||||
| chr19:40694776 | T | A | 1 | a0006c0015t0001g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1209+1213A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694776 | |||||||
| chr19:40694809 | C | T | 1 | a0008c0021t0001g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1209+1180G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694809 | |||||||
| chr19:40694873 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1209+1116C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694873 | |||||||
| chr19:40694916 | G | A | 3 | a0001c0003t0001g0071 a0002c0001t0001g0124 a0002c0001t0001g0149 |
3 | HG02738.hp2 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1209+1073C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40694916 | |||||||
| chr19:40695180 | T | A | 3 | a0001c0002t0004g0342 a0001c0002t0004g0343 a0001c0002t0004g0344 |
3 | HG02886.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1209+809A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695180 | |||||||
| chr19:40695304 | C | A | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+685G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695304 | |||||||
| chr19:40695321 | TA | T | 9 | a0002c0001t0001g0109 a0002c0001t0001g0113 a0002c0001t0001g0140 others(6): Show |
9 | HG00323.hp1 HG01515.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1209+667delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695321 | |||||||
| chr19:40695325 | A | AAAAAAGA others(9): Show |
2 | a0001c0004t0001g0260 a0001c0004t0001g0263 |
2 | HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1209+663_1209+664i others(18): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695325 | |||||||
| chr19:40695326 | A | AAAAAAAA others(9): Show |
9 | a0001c0005t0001g0046 a0001c0005t0001g0047 a0001c0005t0001g0048 others(6): Show |
9 | HG00609.hp1 HG00673.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1209+662_1209+663i others(18): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695326 | |||||||
| chr19:40695326 | A | AAAAAAAA others(8): Show |
150 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(147): Show |
170 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1209+648_1209+662d others(17): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695326 | |||||||
| chr19:40695326 | A | AAAAAAAA others(7): Show |
2 | a0001c0002t0001g0316 a0001c0003t0001g0213 |
2 | HG01256.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1209+662_1209+663i others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695326 | |||||||
| chr19:40695326 | A | AAAAAGAA others(8): Show |
4 | a0001c0004t0001g0240 a0001c0004t0001g0258 a0001c0004t0001g0259 others(1): Show |
4 | HG00639.hp1 HG01175.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+662_1209+663i others(17): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695326 | |||||||
| chr19:40695392 | C | A | 2 | a0001c0002t0001g0275 a0001c0003t0001g0045 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1209+597G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695392 | |||||||
| chr19:40695722 | C | G | 1 | a0002c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1209+267G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695722 | |||||||
| chr19:40695759 | C | T | 1 | a0002c0001t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1209+230G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695759 | |||||||
| chr19:40695865 | G | A | 1 | a0001c0004t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1209+124C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695865 | |||||||
| chr19:40695873 | CTATTATT | C | 24 | a0001c0002t0001g0005 a0001c0002t0001g0077 a0001c0002t0001g0080 others(21): Show |
27 | HG00639.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1209+109_1209+115d others(9): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695873 | |||||||
| chr19:40695947 | G | A | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1209+42C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695947 | |||||||
| chr19:40695955 | C | T | 6 | a0001c0003t0001g0219 a0002c0001t0001g0096 a0002c0001t0001g0097 others(3): Show |
6 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209+34G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 13/14 | chr19 | 40695955 | |||||||
| chr19:40696237 | CT | C | 24 | a0001c0002t0001g0005 a0001c0002t0001g0077 a0001c0002t0001g0080 others(21): Show |
27 | HG00639.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1144-184delA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696237 | |||||||
| chr19:40696245 | T | C | 1 | a0001c0002t0001g0317 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1144-191A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696245 | |||||||
| chr19:40696265 | A | C | 1 | a0002c0001t0001g0294 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1144-211T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696265 | |||||||
| chr19:40696436 | G | T | 3 | a0001c0002t0001g0275 a0001c0003t0001g0045 a0002c0001t0001g0346 |
3 | HG01891.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1144-382C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696436 | |||||||
| chr19:40696664 | C | CA | 34 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0305 others(31): Show |
34 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1144-611dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696664 | |||||||
| chr19:40696664 | C | CAA | 8 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-612_1144-611d others(4): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696664 | |||||||
| chr19:40696664 | CA | C | 11 | a0001c0002t0001g0036 a0001c0002t0001g0311 a0001c0002t0001g0313 others(8): Show |
12 | HG01515.hp2 HG02080.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1144-611delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696664 | |||||||
| chr19:40696706 | G | A | 20 | a0001c0002t0006g0055 a0001c0004t0001g0242 a0001c0004t0001g0244 others(17): Show |
20 | HG00099.hp1 HG00738.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1144-652C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696706 | |||||||
| chr19:40696821 | T | C | 1 | a0001c0018t0003g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1144-767A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40696821 | |||||||
| chr19:40697114 | A | T | 1 | a0002c0001t0001g0116 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1144-1060T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697114 | |||||||
| chr19:40697114 | AT | A | 102 | a0001c0002t0001g0171 a0001c0002t0001g0200 a0001c0002t0001g0217 others(99): Show |
114 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1144-1061delA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697114 | |||||||
| chr19:40697215 | G | A | 1 | a0002c0001t0001g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1144-1161C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697215 | |||||||
| chr19:40697333 | C | T | 1 | a0002c0001t0001g0115 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1144-1279G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697333 | |||||||
| chr19:40697367 | G | A | 1 | a0001c0003t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1144-1313C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697367 | |||||||
| chr19:40697572 | G | A | 1 | a0002c0001t0001g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1144-1518C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697572 | |||||||
| chr19:40697622 | C | A | 1 | a0001c0002t0001g0316 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1144-1568G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697622 | |||||||
| chr19:40697744 | C | T | 1 | a0002c0001t0001g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1144-1690G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697744 | |||||||
| chr19:40697822 | TTA | T | 4 | a0002c0001t0001g0002 a0002c0001t0001g0113 a0002c0001t0001g0138 others(1): Show |
6 | HG00621.hp2 HG02132.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-1770_1144-176 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697822 | |||||||
| chr19:40697824 | A | T | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1144-1770T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697824 | |||||||
| chr19:40697841 | T | G | 3 | a0001c0002t0001g0005 a0002c0001t0001g0034 a0002c0001t0001g0281 |
7 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-1787A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697841 | |||||||
| chr19:40697843 | T | G | 13 | a0001c0002t0001g0005 a0001c0003t0001g0222 a0001c0004t0001g0261 others(10): Show |
18 | HG00642.hp1 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1144-1789A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697843 | |||||||
| chr19:40697843 | T | TAG | 8 | a0002c0001t0001g0023 a0002c0001t0001g0127 a0002c0001t0001g0146 others(5): Show |
9 | HG01123.hp2 HG01256.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1144-1790_1144-178 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697843 | |||||||
| chr19:40697845 | T | G | 46 | a0001c0002t0001g0005 a0001c0002t0001g0324 a0001c0003t0001g0202 others(43): Show |
53 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1144-1791A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697845 | |||||||
| chr19:40697845 | T | TAG | 15 | a0001c0003t0001g0071 a0002c0001t0001g0012 a0002c0001t0001g0022 others(12): Show |
19 | HG00558.hp1 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1144-1792_1144-179 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697845 | |||||||
| chr19:40697845 | T | TAGAG | 3 | a0002c0001t0001g0128 a0002c0001t0001g0129 a0002c0001t0001g0289 |
3 | HG00609.hp2 HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1144-1792_1144-179 others(8): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697845 | |||||||
| chr19:40697847 | T | G | 97 | a0001c0002t0001g0005 a0001c0002t0001g0059 a0001c0002t0001g0061 others(94): Show |
121 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1144-1793A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697847 | |||||||
| chr19:40697847 | T | TAG | 9 | a0002c0001t0001g0008 a0002c0001t0001g0020 a0002c0001t0001g0025 others(6): Show |
14 | HG00099.hp2 HG02683.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144-1794_1144-179 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697847 | |||||||
| chr19:40697849 | T | G | 157 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0054 others(154): Show |
196 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1144-1795A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697849 | |||||||
| chr19:40697849 | T | TAG | 5 | a0002c0001t0001g0092 a0002c0001t0001g0109 a0002c0001t0001g0114 others(2): Show |
5 | HG00323.hp1 HG00733.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-1796_1144-179 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697849 | |||||||
| chr19:40697849 | T | TAGAGAG | 3 | a0001c0004t0001g0238 a0001c0004t0001g0243 a0002c0001t0001g0144 |
3 | HG00140.hp1 HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1144-1796_1144-179 others(10): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697849 | |||||||
| chr19:40697849 | T | TAGAGAGA others(21): Show |
1 | a0001c0002t0001g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1144-1796_1144-179 others(32): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697849 | |||||||
| chr19:40697851 | T | G | 212 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0036 others(209): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1144-1797A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TAGAGAGA others(11): Show |
1 | a0001c0002t0001g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1144-1815_1144-179 others(22): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TAGAGAGA others(25): Show |
1 | a0001c0002t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TAGAGAGA others(35): Show |
1 | a0001c0002t0001g0271 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(46): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(5): Show |
1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(13): Show |
3 | a0001c0002t0001g0322 a0001c0003t0001g0175 a0002c0001t0001g0096 |
3 | HG02970.hp2 NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(15): Show |
2 | a0001c0002t0004g0237 a0002c0001t0001g0099 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(26): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(17): Show |
4 | a0001c0002t0001g0040 a0001c0002t0001g0304 a0001c0002t0001g0316 others(1): Show |
4 | HG01515.hp1 NA18747.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(19): Show |
5 | a0001c0002t0001g0041 a0001c0002t0001g0300 a0001c0002t0001g0301 others(2): Show |
5 | HG00408.hp2 HG01517.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(21): Show |
4 | a0001c0002t0001g0042 a0001c0002t0001g0319 a0001c0004t0001g0249 others(1): Show |
4 | HG00738.hp2 HG01192.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(32): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(23): Show |
3 | a0001c0002t0001g0269 a0001c0002t0001g0293 a0001c0004t0001g0253 |
3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(25): Show |
2 | a0001c0003t0001g0210 a0001c0003t0001g0330 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATAGAGA others(29): Show |
1 | a0001c0003t0001g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(40): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(3): Show |
1 | a0001c0004t0001g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(14): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(5): Show |
2 | a0001c0003t0001g0164 a0001c0007t0001g0241 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(7): Show |
2 | a0001c0003t0001g0178 a0001c0003t0001g0225 |
2 | HG01934.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(18): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(9): Show |
1 | a0001c0002t0001g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(20): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(13): Show |
1 | a0001c0003t0001g0189 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(15): Show |
2 | a0001c0002t0001g0043 a0001c0002t0001g0305 |
2 | HG02602.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(26): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(17): Show |
1 | a0001c0002t0001g0274 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(19): Show |
3 | a0001c0002t0001g0307 a0001c0003t0001g0195 a0002c0023t0001g0062 |
3 | HG02027.hp1 NA18979.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(21): Show |
2 | a0001c0002t0001g0329 a0001c0004t0001g0245 |
2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(32): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(23): Show |
4 | a0001c0002t0001g0233 a0001c0004t0001g0250 a0001c0004t0001g0257 others(1): Show |
4 | HG00735.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(25): Show |
1 | a0001c0003t0001g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(27): Show |
1 | a0001c0012t0001g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(38): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(31): Show |
1 | a0001c0002t0001g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(42): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATAGA others(37): Show |
1 | a0003c0010t0001g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(48): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(5): Show |
1 | a0001c0003t0001g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(9): Show |
1 | a0002c0024t0001g0350 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(20): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(13): Show |
1 | a0001c0005t0001g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(17): Show |
2 | a0001c0002t0001g0306 a0001c0005t0001g0048 |
2 | NA18957.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1144-1798_1144-179 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(19): Show |
1 | a0001c0004t0001g0244 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(23): Show |
1 | a0001c0004t0001g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(37): Show |
1 | a0003c0010t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(48): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(19): Show |
1 | a0001c0002t0001g0077 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(25): Show |
1 | a0001c0004t0001g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(11): Show |
1 | a0001c0003t0001g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(22): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(19): Show |
1 | a0001c0005t0001g0047 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(25): Show |
1 | a0001c0002t0004g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(29): Show |
1 | a0001c0004t0001g0242 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(40): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(35): Show |
1 | a0001c0002t0001g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(46): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(37): Show |
1 | a0001c0002t0004g0344 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(48): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(27): Show |
1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(38): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(33): Show |
1 | a0001c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(44): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(33): Show |
1 | a0001c0002t0004g0343 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(44): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697851 | T | TATATATA others(27): Show |
1 | a0001c0004t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1144-1798_1144-179 others(38): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697851 | |||||||
| chr19:40697853 | G | T | 15 | a0001c0002t0001g0056 a0001c0002t0001g0200 a0001c0002t0001g0231 others(12): Show |
16 | HG00423.hp2 HG00673.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1144-1799C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697853 | |||||||
| chr19:40697864 | A | G | 1 | a0002c0001t0001g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1144-1810T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697864 | |||||||
| chr19:40697866 | A | G | 2 | a0001c0002t0001g0233 a0001c0002t0001g0234 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1144-1812T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697866 | |||||||
| chr19:40697874 | A | AGAGAGAG others(28): Show |
1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1144-1821_1144-182 others(39): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(27): Show |
2 | a0001c0004t0001g0255 a0001c0004t0001g0256 |
2 | HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1144-1821_1144-182 others(38): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(25): Show |
1 | a0001c0004t0001g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1144-1821_1144-182 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(23): Show |
2 | a0001c0004t0001g0265 a0001c0004t0001g0266 |
2 | HG01192.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1144-1821_1144-182 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(21): Show |
3 | a0001c0004t0001g0251 a0001c0004t0001g0252 a0001c0004t0001g0264 |
3 | HG01255.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1144-1821_1144-182 others(32): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(19): Show |
1 | a0001c0004t0001g0248 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1144-1821_1144-182 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | AGAGAGAG others(9): Show |
1 | a0001c0002t0006g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1144-1821_1144-182 others(20): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697874 | A | T | 10 | a0001c0004t0001g0242 a0001c0004t0001g0244 a0001c0004t0001g0245 others(7): Show |
10 | HG00099.hp1 HG00738.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144-1820T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697874 | |||||||
| chr19:40697875 | G | C | 35 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0042 others(32): Show |
35 | HG00408.hp2 HG01192.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.1144-1821C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(17): Show |
1 | a0001c0018t0003g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(7): Show |
1 | a0001c0003t0001g0173 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(18): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(9): Show |
1 | a0001c0002t0001g0275 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(20): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(11): Show |
3 | a0001c0002t0001g0172 a0001c0002t0001g0325 a0001c0003t0001g0069 |
3 | NA18951.hp1 NA18955.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(22): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(13): Show |
5 | a0001c0002t0001g0302 a0001c0002t0001g0341 a0001c0003t0001g0074 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(15): Show |
5 | a0001c0002t0001g0080 a0001c0002t0001g0338 a0001c0002t0001g0340 others(2): Show |
5 | HG01943.hp2 HG04204.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(26): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(17): Show |
9 | a0001c0002t0001g0013 a0001c0002t0001g0036 a0001c0002t0001g0037 others(6): Show |
13 | HG02293.hp2 NA18612.hp1 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(19): Show |
8 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0313 others(5): Show |
8 | HG02080.hp2 HG04115.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(21): Show |
6 | a0001c0002t0001g0312 a0001c0002t0001g0314 a0001c0002t0001g0321 others(3): Show |
6 | HG02071.hp1 NA18975.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(32): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(23): Show |
1 | a0001c0002t0001g0335 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(25): Show |
1 | a0001c0002t0001g0328 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(33): Show |
1 | a0001c0004t0001g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(44): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(31): Show |
1 | a0001c0004t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(42): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(29): Show |
1 | a0001c0004t0001g0260 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(40): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(27): Show |
2 | a0001c0004t0001g0240 a0001c0004t0001g0259 |
2 | HG01496.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(38): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(17): Show |
1 | a0001c0005t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(28): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(25): Show |
2 | a0001c0004t0001g0258 a0001c0020t0001g0232 |
2 | HG00639.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(36): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(15): Show |
3 | a0001c0005t0001g0079 a0001c0005t0001g0081 a0001c0014t0001g0192 |
3 | NA18952.hp2 NA19004.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(26): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(23): Show |
1 | a0001c0002t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1144-1822_1144-182 others(34): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(13): Show |
4 | a0001c0003t0001g0167 a0001c0003t0001g0190 a0001c0003t0001g0211 others(1): Show |
4 | HG00673.hp2 HG01109.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(11): Show |
5 | a0001c0003t0001g0011 a0001c0003t0001g0226 a0001c0005t0001g0078 others(2): Show |
7 | HG00438.hp2 HG00621.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(22): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(13): Show |
3 | a0001c0002t0001g0035 a0001c0002t0001g0297 a0001c0002t0001g0298 |
4 | HG02055.hp2 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(24): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(9): Show |
13 | a0001c0002t0001g0200 a0001c0002t0001g0315 a0001c0003t0001g0029 others(10): Show |
14 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(20): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(7): Show |
29 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0217 others(26): Show |
37 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(18): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(5): Show |
5 | a0001c0003t0001g0026 a0001c0003t0001g0073 a0001c0003t0001g0075 others(2): Show |
6 | HG00733.hp2 HG02976.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(16): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGA others(3): Show |
3 | a0001c0003t0001g0179 a0001c0003t0001g0197 a0001c0003t0001g0203 |
3 | HG01169.hp1 NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(14): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GAGAGAGG others(1): Show |
3 | a0001c0003t0001g0070 a0001c0003t0001g0208 a0002c0001t0001g0349 |
3 | HG02074.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(12): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GGC | 12 | a0001c0003t0001g0163 a0001c0003t0001g0164 a0001c0003t0001g0165 others(9): Show |
12 | HG01884.hp1 HG01934.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(6): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697875 | G | GGGAGAGA others(3): Show |
1 | a0001c0002t0001g0005 | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-1822_1144-182 others(14): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697875 | |||||||
| chr19:40697876 | A | AGAGAGAG others(19): Show |
1 | a0003c0010t0001g0052 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1144-1823_1144-182 others(30): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697876 | |||||||
| chr19:40697876 | A | T | 3 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0053 |
3 | HG00735.hp1 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1144-1822T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697876 | |||||||
| chr19:40697879 | T | G | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-1825A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697879 | |||||||
| chr19:40697913 | C | T | 1 | a0001c0003t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1144-1859G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697913 | |||||||
| chr19:40697953 | T | A | 2 | a0001c0002t0001g0275 a0001c0003t0001g0045 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1144-1899A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40697953 | |||||||
| chr19:40698165 | G | A | 1 | a0002c0001t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1143+1902C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698165 | |||||||
| chr19:40698221 | A | G | 4 | a0001c0003t0001g0069 a0001c0003t0001g0074 a0001c0003t0001g0173 others(1): Show |
4 | HG04228.hp2 NA18980.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+1846T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698221 | |||||||
| chr19:40698229 | G | A | 174 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(171): Show |
194 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1143+1838C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698229 | |||||||
| chr19:40698260 | C | T | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1143+1807G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698260 | |||||||
| chr19:40698442 | G | C | 170 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(167): Show |
190 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1143+1625C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698442 | |||||||
| chr19:40698456 | C | T | 1 | a0002c0001t0001g0101 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1143+1611G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698456 | |||||||
| chr19:40698538 | C | CA | 7 | a0001c0002t0001g0273 a0001c0002t0001g0334 a0002c0001t0001g0066 others(4): Show |
8 | HG01978.hp2 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+1528dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698538 | |||||||
| chr19:40698719 | C | T | 1 | a0001c0002t0001g0299 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1143+1348G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698719 | |||||||
| chr19:40698997 | C | CT | 25 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0336 others(22): Show |
25 | HG00099.hp1 HG00738.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1143+1069dupA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698997 | |||||||
| chr19:40698997 | CT | C | 5 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0061 others(2): Show |
6 | HG02257.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+1069delA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40698997 | |||||||
| chr19:40699074 | A | G | 2 | a0001c0003t0001g0191 a0005c0016t0001g0196 |
2 | HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1143+993T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40699074 | |||||||
| chr19:40699260 | T | C | 205 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(202): Show |
226 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1143+807A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40699260 | |||||||
| chr19:40699406 | G | A | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+661C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40699406 | |||||||
| chr19:40699634 | C | A | 64 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0200 others(61): Show |
76 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1143+433G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40699634 | |||||||
| chr19:40699672 | C | T | 1 | a0001c0003t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1143+395G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 12/14 | chr19 | 40699672 | |||||||
| chr19:40700303 | A | G | 201 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(198): Show |
221 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(218): Show |
splice_region_variant&intron_variant | LOW | c.1035+7T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 11/14 | chr19 | 40700303 | |||||||
| chr19:40700556 | G | A | 2 | a0002c0008t0001g0030 a0002c0008t0001g0228 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.894-105C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40700556 | |||||||
| chr19:40700850 | A | C | 151 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(148): Show |
168 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.894-399T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40700850 | |||||||
| chr19:40700932 | G | C | 1 | a0002c0006t0003g0158 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.894-481C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40700932 | |||||||
| chr19:40700957 | C | T | 1 | a0002c0001t0001g0018 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.894-506G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40700957 | |||||||
| chr19:40701111 | T | C | 1 | a0001c0003t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894-660A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701111 | |||||||
| chr19:40701190 | G | A | 82 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0200 others(79): Show |
93 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.894-739C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701190 | |||||||
| chr19:40701301 | C | G | 6 | a0001c0007t0001g0031 a0001c0007t0001g0241 a0002c0025t0001g0051 others(3): Show |
7 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-850G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701301 | |||||||
| chr19:40701308 | A | G | 8 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-857T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701308 | |||||||
| chr19:40701329 | A | C | 8 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-878T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701329 | |||||||
| chr19:40701394 | T | C | 1 | a0003c0010t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.894-943A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701394 | |||||||
| chr19:40701404 | G | A | 6 | a0002c0001t0001g0286 a0002c0001t0001g0287 a0002c0001t0001g0288 others(3): Show |
6 | HG00609.hp2 NA18942.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.894-953C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701404 | |||||||
| chr19:40701437 | G | C | 83 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0035 others(80): Show |
91 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.894-986C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701437 | |||||||
| chr19:40701457 | T | A | 1 | a0001c0002t0001g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.894-1006A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701457 | |||||||
| chr19:40701480 | G | A | 7 | a0002c0001t0001g0024 a0002c0001t0001g0068 a0002c0001t0001g0090 others(4): Show |
8 | HG02040.hp1 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-1029C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701480 | |||||||
| chr19:40701489 | G | A | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-1038C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701489 | |||||||
| chr19:40701631 | C | T | 1 | a0001c0002t0004g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.893+969G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701631 | |||||||
| chr19:40701914 | G | C | 1 | a0002c0001t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.893+686C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701914 | |||||||
| chr19:40701965 | C | T | 3 | a0001c0002t0004g0342 a0001c0002t0004g0343 a0001c0002t0004g0344 |
3 | HG02886.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.893+635G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40701965 | |||||||
| chr19:40702223 | T | C | 97 | a0001c0002t0001g0005 a0001c0002t0001g0035 a0001c0002t0001g0037 others(94): Show |
103 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.893+377A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40702223 | |||||||
| chr19:40702235 | G | C | 1 | a0001c0002t0001g0340 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.893+365C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40702235 | |||||||
| chr19:40702325 | GTAAT | G | 178 | a0001c0002t0001g0005 a0001c0002t0001g0035 a0001c0002t0001g0037 others(175): Show |
196 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.893+271_893+274del others(4): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40702325 | |||||||
| chr19:40702404 | T | C | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+196A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 10/14 | chr19 | 40702404 | |||||||
| chr19:40702698 | G | C | 2 | a0002c0008t0001g0228 a0002c0008t0001g0278 |
2 | HG02723.hp1 HG03453.hp1 |
splice_region_variant&intron_variant | LOW | c.800-5C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702698 | |||||||
| chr19:40702728 | C | T | 1 | a0001c0003t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.800-35G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702728 | |||||||
| chr19:40702821 | A | ACATCTGT others(45): Show |
1 | a0001c0020t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.800-180_800-129dup others(52): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702821 | |||||||
| chr19:40702821 | A | ACATCTGT others(97): Show |
3 | a0001c0002t0001g0231 a0001c0002t0001g0233 a0001c0002t0001g0234 |
3 | HG01884.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.800-129_800-128ins others(104): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702821 | |||||||
| chr19:40702821 | A | ACATCTGT others(149): Show |
1 | a0001c0002t0001g0005 | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-129_800-128ins others(156): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702821 | |||||||
| chr19:40702899 | G | A | 152 | a0001c0002t0001g0323 a0001c0002t0001g0324 a0001c0002t0001g0325 others(149): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.800-206C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702899 | |||||||
| chr19:40702903 | C | T | 2 | a0001c0004t0001g0277 a0013c0017t0001g0221 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.800-210G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40702903 | |||||||
| chr19:40703004 | G | A | 2 | a0001c0002t0001g0233 a0001c0002t0001g0234 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.800-311C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703004 | |||||||
| chr19:40703076 | C | T | 143 | a0001c0003t0001g0045 a0001c0004t0001g0277 a0002c0001t0001g0001 others(140): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.800-383G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703076 | |||||||
| chr19:40703205 | A | G | 2 | a0001c0002t0004g0237 a0002c0001t0001g0346 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.799+336T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703205 | |||||||
| chr19:40703253 | C | T | 5 | a0001c0003t0001g0173 a0002c0025t0001g0051 a0003c0010t0001g0044 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+288G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703253 | |||||||
| chr19:40703272 | C | T | 27 | a0002c0001t0001g0012 a0002c0001t0001g0016 a0002c0001t0001g0020 others(24): Show |
34 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.799+269G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703272 | |||||||
| chr19:40703278 | T | G | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799+263A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703278 | |||||||
| chr19:40703351 | A | G | 10 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+190T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703351 | |||||||
| chr19:40703426 | C | T | 1 | a0001c0005t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.799+115G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 9/14 | chr19 | 40703426 | |||||||
| chr19:40703630 | G | C | 6 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.718-8C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 8/14 | chr19 | 40703630 | |||||||
| chr19:40703679 | G | T | 1 | a0002c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.717+36C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 8/14 | chr19 | 40703679 | |||||||
| chr19:40703979 | A | AC | 9 | a0001c0002t0001g0339 a0001c0002t0001g0340 a0001c0003t0001g0070 others(6): Show |
9 | HG01978.hp1 HG02027.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-125dupG | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40703979 | |||||||
| chr19:40704111 | G | A | 1 | a0002c0024t0001g0350 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577-256C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704111 | |||||||
| chr19:40704148 | CT | C | 7 | a0001c0002t0001g0326 a0001c0002t0001g0327 a0001c0003t0001g0204 others(4): Show |
7 | HG00140.hp2 HG02451.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-294delA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704148 | |||||||
| chr19:40704358 | C | T | 1 | a0002c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.577-503G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704358 | |||||||
| chr19:40704381 | G | A | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-526C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704381 | |||||||
| chr19:40704444 | C | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-589G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704444 | |||||||
| chr19:40704465 | A | T | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-610T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704465 | |||||||
| chr19:40704587 | G | A | 1 | a0001c0018t0003g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.576+509C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704587 | |||||||
| chr19:40704613 | G | A | 1 | a0002c0001t0001g0138 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.576+483C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704613 | |||||||
| chr19:40704711 | C | T | 9 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.576+385G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704711 | |||||||
| chr19:40704712 | G | A | 7 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(4): Show |
8 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+384C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704712 | |||||||
| chr19:40704732 | C | T | 6 | a0001c0002t0001g0005 a0001c0002t0001g0231 a0001c0002t0001g0233 others(3): Show |
9 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.576+364G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704732 | |||||||
| chr19:40704784 | T | G | 1 | a0002c0001t0001g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.576+312A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704784 | |||||||
| chr19:40704917 | G | C | 1 | a0004c0009t0001g0019 | 2 | NA19012.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.576+179C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 7/14 | chr19 | 40704917 | |||||||
| chr19:40705237 | G | A | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-56C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 6/14 | chr19 | 40705237 | |||||||
| chr19:40705509 | C | T | 1 | a0002c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.368-62G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705509 | |||||||
| chr19:40705511 | G | T | 1 | a0001c0002t0006g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.368-64C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705511 | |||||||
| chr19:40705518 | C | T | 1 | a0001c0012t0001g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368-71G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705518 | |||||||
| chr19:40705698 | C | A | 5 | a0002c0001t0001g0025 a0002c0001t0001g0067 a0002c0001t0001g0159 others(2): Show |
6 | NA18964.hp2 NA18985.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-251G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705698 | |||||||
| chr19:40705744 | C | T | 5 | a0001c0003t0001g0004 a0001c0003t0001g0201 a0001c0003t0001g0202 others(2): Show |
8 | NA18946.hp2 NA18962.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.368-297G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705744 | |||||||
| chr19:40705929 | C | T | 116 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(113): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.368-482G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705929 | |||||||
| chr19:40705932 | G | GA | 13 | a0001c0002t0001g0328 a0001c0002t0001g0329 a0001c0002t0001g0335 others(10): Show |
13 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-486dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705932 | |||||||
| chr19:40705932 | GA | G | 6 | a0001c0002t0001g0299 a0001c0002t0001g0304 a0002c0001t0001g0104 others(3): Show |
7 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-486delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40705932 | |||||||
| chr19:40706083 | G | A | 12 | a0002c0001t0001g0006 a0002c0001t0001g0017 a0002c0001t0001g0086 others(9): Show |
15 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.368-636C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706083 | |||||||
| chr19:40706187 | C | T | 8 | a0002c0001t0001g0007 a0002c0001t0001g0015 a0002c0001t0001g0018 others(5): Show |
12 | HG01167.hp1 HG01169.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.368-740G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706187 | |||||||
| chr19:40706265 | C | G | 1 | a0002c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.368-818G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706265 | |||||||
| chr19:40706283 | G | C | 5 | a0002c0001t0001g0140 a0002c0001t0001g0141 a0002c0001t0001g0142 others(2): Show |
5 | HG01167.hp2 HG01515.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.368-836C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706283 | |||||||
| chr19:40706351 | G | A | 1 | a0010c0027t0005g0038 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.368-904C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706351 | |||||||
| chr19:40706502 | A | G | 1 | a0001c0003t0001g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-1055T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706502 | |||||||
| chr19:40706656 | C | T | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.368-1209G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706656 | |||||||
| chr19:40706670 | G | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.368-1223C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706670 | |||||||
| chr19:40706707 | G | A | 133 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(130): Show |
171 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.368-1260C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706707 | |||||||
| chr19:40706779 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368-1332T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706779 | |||||||
| chr19:40706794 | G | C | 1 | a0002c0001t0001g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.368-1347C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706794 | |||||||
| chr19:40706996 | G | A | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1549C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40706996 | |||||||
| chr19:40707125 | T | C | 227 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(224): Show |
275 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.368-1678A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707125 | |||||||
| chr19:40707269 | A | G | 1 | a0002c0001t0001g0292 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.368-1822T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707269 | |||||||
| chr19:40707317 | T | C | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1870A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707317 | |||||||
| chr19:40707456 | G | GT | 16 | a0002c0001t0001g0006 a0002c0001t0001g0017 a0002c0001t0001g0086 others(13): Show |
19 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.368-2010dupA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707456 | |||||||
| chr19:40707836 | T | C | 10 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+2223A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707836 | |||||||
| chr19:40707878 | A | G | 10 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+2181T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707878 | |||||||
| chr19:40707994 | T | A | 1 | a0002c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367+2065A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40707994 | |||||||
| chr19:40708272 | G | A | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+1787C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708272 | |||||||
| chr19:40708377 | G | A | 11 | a0001c0003t0001g0004 a0001c0003t0001g0168 a0001c0003t0001g0201 others(8): Show |
14 | HG01975.hp1 HG01993.hp2 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.367+1682C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708377 | |||||||
| chr19:40708483 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1576A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708483 | |||||||
| chr19:40708484 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1575A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708484 | |||||||
| chr19:40708485 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1574A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708485 | |||||||
| chr19:40708486 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1573T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708486 | |||||||
| chr19:40708487 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1572T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708487 | |||||||
| chr19:40708488 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1571A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708488 | |||||||
| chr19:40708489 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1570A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708489 | |||||||
| chr19:40708491 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1568A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708491 | |||||||
| chr19:40708501 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1558T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708501 | |||||||
| chr19:40708522 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1537A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708522 | |||||||
| chr19:40708527 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1532G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708527 | |||||||
| chr19:40708528 | A | AC | 10 | a0001c0002t0001g0077 a0001c0002t0001g0080 a0001c0005t0001g0046 others(7): Show |
10 | HG00609.hp1 HG00673.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+1530dupG | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708528 | |||||||
| chr19:40708531 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1528A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708531 | |||||||
| chr19:40708532 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1527T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708532 | |||||||
| chr19:40708536 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1523G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708536 | |||||||
| chr19:40708541 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1518A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708541 | |||||||
| chr19:40708543 | A | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1516T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708543 | |||||||
| chr19:40708544 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1515G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708544 | |||||||
| chr19:40708549 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1510G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708549 | |||||||
| chr19:40708553 | G | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1506C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708553 | |||||||
| chr19:40708554 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1505T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708554 | |||||||
| chr19:40708558 | G | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1501C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708558 | |||||||
| chr19:40708559 | G | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1500C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708559 | |||||||
| chr19:40708561 | A | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1498T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708561 | |||||||
| chr19:40708563 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1496T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708563 | |||||||
| chr19:40708566 | G | C | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367+1493C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708566 | |||||||
| chr19:40708567 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1492C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708567 | |||||||
| chr19:40708569 | G | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1490C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708569 | |||||||
| chr19:40708574 | G | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1485C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708574 | |||||||
| chr19:40708578 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1481G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708578 | |||||||
| chr19:40708580 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1479C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708580 | |||||||
| chr19:40708592 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1467G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708592 | |||||||
| chr19:40708593 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1466G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708593 | |||||||
| chr19:40708594 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1465T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708594 | |||||||
| chr19:40708597 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1462G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708597 | |||||||
| chr19:40708598 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1461G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708598 | |||||||
| chr19:40708599 | C | G | 3 | a0002c0001t0001g0016 a0002c0001t0001g0091 a0002c0001t0001g0092 |
4 | HG00733.hp1 HG00741.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1460G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708599 | |||||||
| chr19:40708601 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1458T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708601 | |||||||
| chr19:40708602 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1457T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708602 | |||||||
| chr19:40708604 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1455G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708604 | |||||||
| chr19:40708605 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1454G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708605 | |||||||
| chr19:40708608 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1451G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708608 | |||||||
| chr19:40708609 | A | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1450T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708609 | |||||||
| chr19:40708610 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1449G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708610 | |||||||
| chr19:40708611 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1448G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708611 | |||||||
| chr19:40708613 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1446T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708613 | |||||||
| chr19:40708614 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1445G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708614 | |||||||
| chr19:40708615 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1444G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708615 | |||||||
| chr19:40708616 | C | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1443G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708616 | |||||||
| chr19:40708619 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1440T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708619 | |||||||
| chr19:40708620 | A | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1439T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708620 | |||||||
| chr19:40708621 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1438G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708621 | |||||||
| chr19:40708626 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1433A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708626 | |||||||
| chr19:40708629 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1430A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708629 | |||||||
| chr19:40708630 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1429A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708630 | |||||||
| chr19:40708631 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1428A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708631 | |||||||
| chr19:40708641 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1418T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708641 | |||||||
| chr19:40708644 | C | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1415G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708644 | |||||||
| chr19:40708645 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1414T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708645 | |||||||
| chr19:40708649 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1410A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708649 | |||||||
| chr19:40708653 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1406A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708653 | |||||||
| chr19:40708655 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1404A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708655 | |||||||
| chr19:40708663 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1396G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708663 | |||||||
| chr19:40708665 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1394A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708665 | |||||||
| chr19:40708669 | T | G | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1390A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708669 | |||||||
| chr19:40708682 | C | T | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1377G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708682 | |||||||
| chr19:40708685 | T | C | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1374A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708685 | |||||||
| chr19:40708686 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1373C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708686 | |||||||
| chr19:40708693 | T | A | 1 | a0002c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.367+1366A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708693 | |||||||
| chr19:40708698 | A | AGGGAGGA others(12): Show |
1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.367+1342_367+1360d others(21): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708698 | |||||||
| chr19:40708761 | CTACAAAA others(2): Show |
C | 7 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+1289_367+1297d others(11): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708761 | |||||||
| chr19:40708819 | T | C | 6 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+1240A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708819 | |||||||
| chr19:40708891 | T | C | 146 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(143): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.367+1168A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708891 | |||||||
| chr19:40708930 | C | CA | 136 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(133): Show |
175 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.367+1128dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708930 | |||||||
| chr19:40708932 | A | G | 2 | a0001c0005t0001g0078 a0001c0005t0001g0079 |
2 | NA18969.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.367+1127T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40708932 | |||||||
| chr19:40709027 | T | C | 55 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(52): Show |
60 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.367+1032A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709027 | |||||||
| chr19:40709318 | T | G | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.367+741A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709318 | |||||||
| chr19:40709357 | C | A | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+702G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709357 | |||||||
| chr19:40709430 | G | A | 5 | a0002c0001t0001g0346 a0002c0001t0001g0347 a0002c0001t0001g0348 others(2): Show |
5 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+629C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709430 | |||||||
| chr19:40709559 | A | C | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367+500T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709559 | |||||||
| chr19:40709562 | T | C | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+497A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709562 | |||||||
| chr19:40709750 | G | A | 6 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+309C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709750 | |||||||
| chr19:40709790 | C | G | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+269G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709790 | |||||||
| chr19:40709964 | C | T | 1 | a0001c0002t0001g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.367+95G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 5/14 | chr19 | 40709964 | |||||||
| chr19:40710253 | T | A | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290-117A>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710253 | |||||||
| chr19:40710254 | C | A | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290-118G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710254 | |||||||
| chr19:40710267 | T | C | 344 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(341): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.290-131A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710267 | |||||||
| chr19:40710392 | G | A | 6 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-256C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710392 | |||||||
| chr19:40710422 | G | A | 1 | a0001c0003t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.290-286C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710422 | |||||||
| chr19:40710450 | G | A | 1 | a0001c0002t0004g0237 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290-314C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710450 | |||||||
| chr19:40710767 | T | G | 1 | a0001c0003t0001g0074 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.290-631A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710767 | |||||||
| chr19:40710854 | G | A | 6 | a0002c0001t0001g0286 a0002c0001t0001g0287 a0002c0001t0001g0288 others(3): Show |
6 | HG00609.hp2 NA18942.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-718C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710854 | |||||||
| chr19:40710897 | C | T | 2 | a0002c0001t0001g0347 a0002c0001t0001g0348 |
2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.290-761G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710897 | |||||||
| chr19:40710900 | G | A | 3 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0223 |
3 | HG02602.hp2 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.290-764C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710900 | |||||||
| chr19:40710929 | C | T | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-793G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710929 | |||||||
| chr19:40710935 | C | T | 1 | a0013c0017t0001g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290-799G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710935 | |||||||
| chr19:40710984 | A | G | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-848T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40710984 | |||||||
| chr19:40711131 | C | CA | 6 | a0001c0003t0001g0073 a0001c0003t0001g0211 a0001c0003t0001g0212 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-996dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711131 | |||||||
| chr19:40711131 | CA | C | 138 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(135): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.290-996delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711131 | |||||||
| chr19:40711131 | CAA | C | 134 | a0001c0002t0001g0304 a0001c0002t0001g0332 a0001c0004t0001g0239 others(131): Show |
172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.290-997_290-996del others(2): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711131 | |||||||
| chr19:40711298 | C | T | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-1162G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711298 | |||||||
| chr19:40711333 | G | A | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-1197C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711333 | |||||||
| chr19:40711677 | G | A | 1 | a0002c0001t0001g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.290-1541C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711677 | |||||||
| chr19:40711696 | G | A | 1 | a0001c0005t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.290-1560C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40711696 | |||||||
| chr19:40712027 | AT | A | 6 | a0001c0003t0001g0216 a0002c0001t0001g0290 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-1892delA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712027 | |||||||
| chr19:40712246 | G | C | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+1821C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712246 | |||||||
| chr19:40712317 | G | A | 56 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(53): Show |
61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.289+1750C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712317 | |||||||
| chr19:40712350 | G | T | 32 | a0001c0004t0001g0238 a0001c0004t0001g0239 a0001c0004t0001g0240 others(29): Show |
33 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(30): Show |
intron_variant | MODIFIER | c.289+1717C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712350 | |||||||
| chr19:40712362 | C | T | 1 | a0001c0004t0001g0238 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.289+1705G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712362 | |||||||
| chr19:40712411 | A | AG | 9 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(6): Show |
10 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+1655dupC | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712411 | |||||||
| chr19:40712412 | G | GA | 73 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(70): Show |
78 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.289+1654dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712412 | |||||||
| chr19:40712412 | G | GAA | 7 | a0001c0002t0001g0042 a0001c0002t0001g0300 a0001c0002t0001g0335 others(4): Show |
7 | HG00597.hp2 HG01192.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+1653_289+1654d others(4): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712412 | |||||||
| chr19:40712412 | GA | G | 17 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(14): Show |
18 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.289+1654delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712412 | |||||||
| chr19:40712413 | A | G | 6 | a0002c0001t0001g0088 a0002c0001t0001g0089 a0002c0001t0001g0345 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+1654T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712413 | |||||||
| chr19:40712428 | A | C | 1 | a0002c0001t0001g0087 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.289+1639T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712428 | |||||||
| chr19:40712430 | C | A | 1 | a0002c0001t0001g0151 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.289+1637G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712430 | |||||||
| chr19:40712443 | T | C | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+1624A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712443 | |||||||
| chr19:40712554 | C | T | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+1513G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712554 | |||||||
| chr19:40712618 | A | G | 1 | a0002c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.289+1449T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712618 | |||||||
| chr19:40712620 | G | A | 4 | a0001c0004t0001g0264 a0001c0004t0001g0265 a0001c0004t0001g0266 others(1): Show |
4 | HG00741.hp2 HG01192.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1447C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712620 | |||||||
| chr19:40712706 | G | A | 218 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(215): Show |
266 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.289+1361C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712706 | |||||||
| chr19:40712901 | C | T | 1 | a0001c0003t0001g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.289+1166G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712901 | |||||||
| chr19:40712980 | G | A | 1 | a0013c0017t0001g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289+1087C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712980 | |||||||
| chr19:40712994 | G | A | 2 | a0002c0006t0003g0152 a0002c0006t0003g0230 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.289+1073C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40712994 | |||||||
| chr19:40713275 | C | G | 1 | a0002c0001t0001g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.289+792G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713275 | |||||||
| chr19:40713335 | G | A | 5 | a0002c0001t0002g0009 a0002c0001t0002g0153 a0002c0001t0002g0154 others(2): Show |
7 | HG00642.hp2 HG01433.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+732C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713335 | |||||||
| chr19:40713505 | C | T | 1 | a0002c0001t0001g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.289+562G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713505 | |||||||
| chr19:40713520 | G | A | 1 | a0001c0003t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.289+547C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713520 | |||||||
| chr19:40713521 | C | A | 81 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(78): Show |
90 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.289+546G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713521 | |||||||
| chr19:40713566 | A | AT | 5 | a0001c0002t0001g0332 a0001c0002t0001g0333 a0001c0002t0001g0334 others(2): Show |
5 | HG00597.hp2 NA18984.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+500_289+501ins others(1): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713566 | |||||||
| chr19:40713566 | A | T | 213 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0014 others(210): Show |
261 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.289+501T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713566 | |||||||
| chr19:40713653 | T | C | 1 | a0013c0017t0001g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289+414A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713653 | |||||||
| chr19:40713681 | A | ACCGT | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+385_289+386ins others(4): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713681 | |||||||
| chr19:40713685 | C | CTG | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+381_289+382ins others(2): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713685 | |||||||
| chr19:40713688 | C | A | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+379G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713688 | |||||||
| chr19:40713690 | T | TC | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+376_289+377ins others(1): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713690 | |||||||
| chr19:40713691 | G | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+376C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713691 | |||||||
| chr19:40713693 | G | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+374C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713693 | |||||||
| chr19:40713695 | A | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+372T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713695 | |||||||
| chr19:40713696 | A | C | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+371T>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713696 | |||||||
| chr19:40713698 | A | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+369T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713698 | |||||||
| chr19:40713701 | G | GACTCTGT others(4): Show |
8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+365_289+366ins others(11): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713701 | |||||||
| chr19:40713702 | C | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0054 a0001c0002t0001g0056 others(5): Show |
9 | HG01123.hp1 HG02257.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+365G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713702 | |||||||
| chr19:40713720 | G | GA | 6 | a0001c0002t0001g0042 a0001c0002t0001g0340 a0001c0003t0001g0222 others(3): Show |
6 | HG01192.hp1 HG02602.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+346dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713720 | |||||||
| chr19:40713742 | G | A | 1 | a0001c0002t0001g0336 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.289+325C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713742 | |||||||
| chr19:40713747 | G | A | 5 | a0002c0006t0003g0158 a0002c0025t0001g0051 a0003c0010t0001g0044 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+320C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713747 | |||||||
| chr19:40713797 | T | C | 1 | a0001c0003t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.289+270A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713797 | |||||||
| chr19:40713876 | C | CA | 11 | a0001c0002t0001g0061 a0001c0002t0001g0337 a0001c0002t0001g0338 others(8): Show |
11 | HG02257.hp2 NA18949.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.289+190dupT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713876 | |||||||
| chr19:40713876 | CA | C | 6 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0002c0001t0001g0084 others(3): Show |
6 | HG01943.hp1 HG03579.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+190delT | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713876 | |||||||
| chr19:40713913 | T | C | 5 | a0002c0001t0001g0025 a0002c0001t0001g0067 a0002c0001t0001g0159 others(2): Show |
6 | NA18964.hp2 NA18985.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+154A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 4/14 | chr19 | 40713913 | |||||||
| chr19:40714149 | AAGGTCTG | A | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-23_223-17delCA others(5): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 3/14 | chr19 | 40714149 | |||||||
| chr19:40714459 | C | G | 4 | a0002c0025t0001g0051 a0003c0010t0001g0044 a0003c0010t0001g0052 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-62G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 2/14 | chr19 | 40714459 | |||||||
| chr19:40714698 | T | C | 1 | a0002c0001t0001g0346 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-3-63A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40714698 | |||||||
| chr19:40714800 | A | T | 1 | a0001c0002t0001g0077 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3-165T>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40714800 | |||||||
| chr19:40714822 | C | G | 3 | a0002c0008t0001g0030 a0002c0008t0001g0228 a0002c0008t0001g0278 |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-187G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40714822 | |||||||
| chr19:40714831 | C | A | 1 | a0001c0002t0001g0300 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-3-196G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40714831 | |||||||
| chr19:40715083 | T | C | 1 | a0002c0024t0001g0350 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-448A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715083 | |||||||
| chr19:40715093 | C | G | 3 | a0001c0003t0001g0163 a0001c0003t0001g0164 a0001c0003t0001g0165 |
3 | HG01884.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-3-458G>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715093 | |||||||
| chr19:40715116 | G | A | 1 | a0001c0004t0001g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3-481C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715116 | |||||||
| chr19:40715153 | G | A | 1 | a0002c0001t0001g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-3-518C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715153 | |||||||
| chr19:40715314 | C | T | 1 | a0002c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-3-679G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715314 | |||||||
| chr19:40715325 | C | T | 1 | a0002c0001t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-3-690G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715325 | |||||||
| chr19:40715431 | C | T | 1 | a0001c0005t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-3-796G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715431 | |||||||
| chr19:40715581 | C | A | 24 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0054 others(21): Show |
28 | HG00609.hp1 HG01123.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-3-946G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715581 | |||||||
| chr19:40715582 | C | T | 1 | a0001c0002t0004g0237 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3-947G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715582 | |||||||
| chr19:40715608 | G | C | 136 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(133): Show |
175 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-3-973C>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715608 | |||||||
| chr19:40715841 | T | TTC | 7 | a0001c0002t0001g0005 a0001c0002t0001g0231 a0001c0002t0001g0233 others(4): Show |
10 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-4+744_-4+745dupGA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715841 | |||||||
| chr19:40715845 | C | CTG | 166 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(163): Show |
203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-4+740_-4+741dupCA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715845 | |||||||
| chr19:40715845 | C | CTGTG | 25 | a0001c0002t0001g0014 a0001c0002t0001g0040 a0001c0002t0001g0041 others(22): Show |
27 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-4+738_-4+741dupCA others(2): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715845 | |||||||
| chr19:40715845 | C | CTGTGTG | 9 | a0001c0003t0001g0045 a0001c0005t0001g0046 a0001c0005t0001g0047 others(6): Show |
9 | HG03579.hp1 NA18947.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+736_-4+741dupCA others(4): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715845 | |||||||
| chr19:40715845 | CTG | C | 61 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0002t0001g0270 others(58): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-4+740_-4+741delCA | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715845 | |||||||
| chr19:40715870 | T | C | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4+717A>G | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715870 | |||||||
| chr19:40715870 | T | TGTGTGTG others(5): Show |
3 | a0001c0002t0004g0342 a0001c0002t0004g0343 a0001c0002t0004g0344 |
3 | HG02886.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4+716_-4+717insGC others(10): Show |
COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715870 | |||||||
| chr19:40715918 | C | T | 4 | a0001c0002t0001g0035 a0001c0002t0001g0296 a0001c0002t0001g0297 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+669G>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715918 | |||||||
| chr19:40715925 | C | A | 2 | a0002c0001t0001g0294 a0002c0001t0001g0295 |
2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-4+662G>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40715925 | |||||||
| chr19:40716014 | G | A | 57 | a0001c0002t0001g0013 a0001c0002t0001g0035 a0001c0002t0001g0036 others(54): Show |
62 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-4+573C>T | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40716014 | |||||||
| chr19:40716151 | G | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0042 others(1): Show |
4 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+436C>A | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40716151 | |||||||
| chr19:40716320 | A | G | 1 | a0002c0001t0001g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-4+267T>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40716320 | |||||||
| chr19:40716358 | T | G | 6 | a0002c0001t0001g0345 a0002c0001t0001g0346 a0002c0001t0001g0347 others(3): Show |
6 | HG02622.hp1 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+229A>C | COQ8B | ENSG00000123815.13 | transcript | ENST00000324464.8 | protein_coding | 1/14 | chr19 | 40716358 |