Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51805 |
| ensemblid | ENSG00000132423.12 |
| hgncid | 18175 |
| symbol | COQ3 |
| name | coenzyme Q3, methyltransferase |
| refseq_nuc | NM_017421.4 |
| refseq_prot | NP_059117.3 |
| ensembl_nuc | ENST00000254759.8 |
| ensembl_prot | ENSP00000254759.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 99369401 |
| end | 99394195 |
| strand | - |
| ver | v1.2 |
| region | chr6:99369401-99394195 |
| region5000 | chr6:99364401-99399195 |
| regionname0 | COQ3_chr6_99369401_99394195 |
| regionname5000 | COQ3_chr6_99364401_99399195 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 369 | 214 | 38 | 63 | 79 | 5 | 29 | 70 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0002 | 0/1 | 369 | 135 | 24 | 16 | 75 | 7 | 12 | 56 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0003 | 0/0 | 369 | 59 | 7 | 5 | 39 | 6 | 2 | 33 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0004 | 1/0 | 369 | 19 | 15 | 3 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0005 | 0/0 | 369 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0006 | 0/0 | 369 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0007 | 0/0 | 369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| a0008 | 0/0 | 369 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | MWSGR others(364): Show |
chr6 | 99364401 | 99399195 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1107 | 213 | 38 | 63 | 78 | 5 | 29 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0001c0006 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0002c0002 | 0/1 | 1107 | 135 | 24 | 16 | 75 | 7 | 12 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0003c0003 | 0/0 | 1107 | 59 | 7 | 5 | 39 | 6 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0004c0004 | 1/0 | 1107 | 19 | 15 | 3 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0005c0005 | 0/0 | 1107 | 4 | 4 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0006c0008 | 0/0 | 1107 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0007c0009 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 | ||
| a0008c0007 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | ATGTG others(1102): Show |
chr6 | 99364401 | 99399195 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1326 | 138 | 35 | 41 | 35 | 5 | 22 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0001c0001t0002 | 0/0 | 1326 | 75 | 3 | 22 | 43 | 0 | 7 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0001c0006t0002 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0002c0002t0001 | 0/1 | 1326 | 97 | 15 | 12 | 55 | 3 | 11 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0002c0002t0002 | 0/0 | 1326 | 38 | 9 | 4 | 20 | 4 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0003c0003t0003 | 0/0 | 1325 | 51 | 7 | 5 | 31 | 6 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1320): Show |
chr6 | 99364401 | 99399195 |
| a0003c0003t0004 | 0/0 | 1325 | 8 | 0 | 0 | 8 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1320): Show |
chr6 | 99364401 | 99399195 |
| a0004c0004t0003 | 1/0 | 1325 | 19 | 15 | 3 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1320): Show |
chr6 | 99364401 | 99399195 |
| a0005c0005t0003 | 0/0 | 1325 | 4 | 4 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1320): Show |
chr6 | 99364401 | 99399195 |
| a0006c0008t0002 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0007c0009t0001 | 0/0 | 1326 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1321): Show |
chr6 | 99364401 | 99399195 |
| a0008c0007t0004 | 0/0 | 1325 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | GGGAT others(1320): Show |
chr6 | 99364401 | 99399195 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 8 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 4 | 1 | 0 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0001c0006t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0001 | 0/0 | 16 | 0 | 1 | 14 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0014 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0010 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0003c0003t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0004c0004t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0005c0005t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0005c0005t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0005c0005t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0005c0005t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0006c0008t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0007c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| a0008c0007t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0248 | EUR | GBR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00140 | hp1 | a0003 | c0003 | t0003 | g0144 | EUR | GBR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0014 | EUR | GBR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0311 | EUR | FIN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00544 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00609 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00621 | hp1 | a0003 | c0003 | t0004 | g0251 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00621 | hp2 | a0003 | c0003 | t0003 | g0140 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | CHS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00735 | hp1 | a0004 | c0004 | t0003 | g0076 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG00741 | hp2 | a0003 | c0003 | t0003 | g0150 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01099 | hp2 | a0004 | c0004 | t0003 | g0214 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01109 | hp2 | a0004 | c0004 | t0003 | g0070 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0136 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0241 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01169 | hp2 | a0003 | c0003 | t0003 | g0137 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0147 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01496 | hp1 | a0006 | c0008 | t0002 | g0242 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01515 | hp1 | a0003 | c0003 | t0003 | g0156 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0246 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01516 | hp1 | a0003 | c0003 | t0003 | g0010 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0149 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01517 | hp1 | a0003 | c0003 | t0003 | g0018 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0158 | EUR | IBS | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02055 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0226 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02071 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02074 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | CDX | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CDX | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | CDX | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02258 | hp2 | a0005 | c0005 | t0003 | g0217 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02622 | hp2 | a0004 | c0004 | t0003 | g0164 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0067 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02886 | hp2 | a0004 | c0004 | t0003 | g0073 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02895 | hp1 | a0004 | c0004 | t0003 | g0222 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0249 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0225 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0229 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02897 | hp2 | a0004 | c0004 | t0003 | g0223 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0216 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02922 | hp2 | a0005 | c0005 | t0003 | g0218 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02965 | hp1 | a0004 | c0004 | t0003 | g0163 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0305 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03041 | hp1 | a0004 | c0004 | t0003 | g0072 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03041 | hp2 | a0004 | c0004 | t0003 | g0215 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0252 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03098 | hp2 | a0004 | c0004 | t0003 | g0068 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0257 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03453 | hp1 | a0005 | c0005 | t0003 | g0059 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0022 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03486 | hp1 | a0005 | c0005 | t0003 | g0219 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03516 | hp2 | a0004 | c0004 | t0003 | g0022 | AFR | ESN | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0304 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03669 | hp2 | a0003 | c0003 | t0003 | g0010 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04204 | hp1 | a0007 | c0009 | t0001 | g0058 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | STU | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | CHB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18942 | hp2 | a0003 | c0003 | t0004 | g0260 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18944 | hp1 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18946 | hp2 | a0003 | c0003 | t0003 | g0155 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18949 | hp2 | a0003 | c0003 | t0003 | g0189 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18956 | hp1 | a0003 | c0003 | t0004 | g0269 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18959 | hp1 | a0003 | c0003 | t0003 | g0042 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0143 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18961 | hp2 | a0003 | c0003 | t0003 | g0134 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18967 | hp1 | a0003 | c0003 | t0003 | g0042 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0139 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18975 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18977 | hp1 | a0003 | c0003 | t0003 | g0032 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18978 | hp1 | a0003 | c0003 | t0004 | g0250 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18979 | hp2 | a0003 | c0003 | t0003 | g0087 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18980 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18983 | hp1 | a0003 | c0003 | t0003 | g0018 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18984 | hp2 | a0003 | c0003 | t0003 | g0151 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18987 | hp1 | a0003 | c0003 | t0003 | g0145 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18987 | hp2 | a0008 | c0007 | t0004 | g0245 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18989 | hp1 | a0001 | c0006 | t0002 | g0276 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18991 | hp2 | a0003 | c0003 | t0003 | g0032 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18992 | hp1 | a0003 | c0003 | t0003 | g0157 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18994 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18998 | hp1 | a0003 | c0003 | t0004 | g0244 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19002 | hp2 | a0003 | c0003 | t0004 | g0310 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19003 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19009 | hp2 | a0003 | c0003 | t0004 | g0238 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19010 | hp2 | a0003 | c0003 | t0003 | g0135 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19030 | hp2 | a0004 | c0004 | t0003 | g0166 | AFR | LWK | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0255 | AFR | LWK | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19043 | hp2 | a0004 | c0004 | t0003 | g0221 | AFR | LWK | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19076 | hp1 | a0003 | c0003 | t0004 | g0243 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19076 | hp2 | a0003 | c0003 | t0003 | g0018 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19078 | hp2 | a0003 | c0003 | t0003 | g0148 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19087 | hp2 | a0003 | c0003 | t0003 | g0202 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0153 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | YRI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0138 | AFR | ASW | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20129 | hp2 | a0004 | c0004 | t0003 | g0167 | AFR | ASW | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0108 | EUR | TSI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20805 | hp2 | a0003 | c0003 | t0003 | g0010 | EUR | TSI | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | GIH | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20905 | hp2 | a0003 | c0003 | t0003 | g0210 | SAS | GIH | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG01123 | hp2 | a0003 | c0003 | t0003 | g0152 | AMR | CLM | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0227 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02559 | hp1 | a0004 | c0004 | t0003 | g0165 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | ACB | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | USA | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0204 | REF | REF | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0003 | g0069 | REF | REF | COQ3_chr6_99364401_99399195 | COQ3 | chr6 | 99364401 | 99399195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99369725 | A | G | 7 | a0001 a0002 a0003 others(4): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
missense_variant | MODERATE | c.985T>C | p.Tyr329His | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 7/7 | 1001/1325 | 985/1110 | 329/369 | chr6 | 99369725 | |||
| chr6:99369809 | C | T | 1 | a0006 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.901G>A | p.Val301Ile | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 7/7 | 917/1325 | 901/1110 | 301/369 | chr6 | 99369809 | |||
| chr6:99371503 | T | C | 4 | a0001 a0002 a0006 others(1): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
missense_variant | MODERATE | c.814A>G | p.Ser272Gly | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/7 | 830/1325 | 814/1110 | 272/369 | chr6 | 99371503 | |||
| chr6:99371527 | T | A | 1 | a0008 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.790A>T | p.Ile264Phe | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/7 | 806/1325 | 790/1110 | 264/369 | chr6 | 99371527 | |||
| chr6:99377472 | T | C | 2 | a0002 a0006 |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
missense_variant | MODERATE | c.400A>G | p.Lys134Glu | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/7 | 416/1325 | 400/1110 | 134/369 | chr6 | 99377472 | |||
| chr6:99380330 | G | A | 1 | a0005 | 4 | HG02258.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.245C>T | p.Ala82Val | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/7 | 261/1325 | 245/1110 | 82/369 | chr6 | 99380330 | |||
| chr6:99383709 | T | C | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.222A>G | p.Ile74Met | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/7 | 238/1325 | 222/1110 | 74/369 | chr6 | 99383709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99380233 | A | G | 1 | a0001c0006 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.342T>C | p.Tyr114Tyr | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/7 | 358/1325 | 342/1110 | 114/369 | chr6 | 99380233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99369543 | T | TC | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0006t0002 others(4): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*56_*57insG | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 7/7 | 56 | chr6 | 99369543 | ||||||
| chr6:99394180 | C | A | 6 | a0001c0001t0002 a0001c0006t0002 a0002c0002t0002 others(3): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/7 | 1 | chr6 | 99394180 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99369823 | GA | G | 8 | a0001c0001t0001g0104 a0003c0003t0003g0139 a0003c0003t0003g0143 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02809.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.890-4delT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99369823 | |||||||
| chr6:99369837 | T | A | 9 | a0003c0003t0003g0189 a0003c0003t0003g0202 a0003c0003t0004g0238 others(6): Show |
9 | HG00621.hp1 NA18949.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.890-17A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99369837 | |||||||
| chr6:99370022 | G | A | 2 | a0004c0004t0003g0222 a0004c0004t0003g0223 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.890-202C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370022 | |||||||
| chr6:99370032 | A | G | 3 | a0001c0001t0002g0297 a0001c0001t0002g0302 a0001c0001t0002g0303 |
3 | NA18967.hp2 NA19058.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.890-212T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370032 | |||||||
| chr6:99370050 | A | G | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.890-230T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370050 | |||||||
| chr6:99370052 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(142): Show |
191 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.890-232C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370052 | |||||||
| chr6:99370080 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(292): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.890-260A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370080 | |||||||
| chr6:99370225 | G | A | 3 | a0002c0002t0002g0304 a0002c0002t0002g0305 a0002c0002t0002g0311 |
3 | HG00280.hp2 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.890-405C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370225 | |||||||
| chr6:99370316 | C | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.890-496G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370316 | |||||||
| chr6:99370344 | C | CT | 9 | a0003c0003t0003g0067 a0003c0003t0003g0075 a0003c0003t0003g0225 others(6): Show |
9 | HG01099.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.890-525dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | C | CTT | 8 | a0001c0001t0001g0116 a0001c0001t0001g0212 a0003c0003t0003g0226 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.890-526_890-525dup others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | C | CTTT | 121 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(118): Show |
162 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.890-527_890-525dup others(3): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | C | CTTTT | 30 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0043 others(27): Show |
35 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.890-528_890-525dup others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | CT | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
27 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.890-525delA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | CTT | C | 72 | a0001c0001t0002g0285 a0002c0002t0001g0001 a0002c0002t0001g0004 others(69): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.890-526_890-525del others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370344 | CTTT | C | 9 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0095 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.890-527_890-525del others(3): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370344 | |||||||
| chr6:99370438 | T | C | 1 | a0003c0003t0003g0146 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.890-618A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370438 | |||||||
| chr6:99370569 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.890-749C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370569 | |||||||
| chr6:99370640 | C | T | 79 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0033 others(76): Show |
102 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.889+788G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370640 | |||||||
| chr6:99370837 | T | C | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.889+591A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370837 | |||||||
| chr6:99370881 | G | A | 1 | a0002c0002t0001g0031 | 2 | HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.889+547C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99370881 | |||||||
| chr6:99371058 | G | A | 1 | a0003c0003t0003g0157 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.889+370C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99371058 | |||||||
| chr6:99371215 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.889+213G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99371215 | |||||||
| chr6:99371252 | A | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.889+176T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99371252 | |||||||
| chr6:99371285 | T | C | 1 | a0003c0003t0003g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.889+143A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99371285 | |||||||
| chr6:99371311 | C | T | 9 | a0003c0003t0003g0075 a0003c0003t0003g0225 a0003c0003t0003g0226 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.889+117G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 6/6 | chr6 | 99371311 | |||||||
| chr6:99371606 | T | C | 19 | a0002c0002t0001g0039 a0002c0002t0001g0114 a0002c0002t0001g0126 others(16): Show |
24 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.730-19A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371606 | |||||||
| chr6:99371680 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.730-93G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371680 | |||||||
| chr6:99371714 | C | T | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.730-127G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371714 | |||||||
| chr6:99371869 | A | G | 1 | a0004c0004t0003g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.730-282T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371869 | |||||||
| chr6:99371883 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.730-296T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371883 | |||||||
| chr6:99371935 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.730-348A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99371935 | |||||||
| chr6:99372279 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.730-692G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372279 | |||||||
| chr6:99372312 | G | A | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.730-725C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372312 | |||||||
| chr6:99372361 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.730-774A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372361 | |||||||
| chr6:99372423 | C | T | 4 | a0005c0005t0003g0059 a0005c0005t0003g0217 a0005c0005t0003g0218 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-836G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372423 | |||||||
| chr6:99372564 | C | T | 9 | a0003c0003t0003g0075 a0003c0003t0003g0225 a0003c0003t0003g0226 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.730-977G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372564 | |||||||
| chr6:99372574 | C | T | 1 | a0004c0004t0003g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.730-987G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372574 | |||||||
| chr6:99372696 | A | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.730-1109T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372696 | |||||||
| chr6:99372712 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.730-1125C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372712 | |||||||
| chr6:99372789 | G | T | 2 | a0003c0003t0003g0225 a0003c0003t0003g0229 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730-1202C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372789 | |||||||
| chr6:99372830 | GA | G | 4 | a0005c0005t0003g0059 a0005c0005t0003g0217 a0005c0005t0003g0218 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-1244delT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372830 | |||||||
| chr6:99372879 | T | C | 85 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(82): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.730-1292A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372879 | |||||||
| chr6:99372909 | A | C | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.730-1322T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372909 | |||||||
| chr6:99372971 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-1384C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99372971 | |||||||
| chr6:99373245 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.730-1658G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373245 | |||||||
| chr6:99373339 | G | C | 31 | a0003c0003t0003g0003 a0003c0003t0003g0010 a0003c0003t0003g0018 others(28): Show |
45 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.730-1752C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373339 | |||||||
| chr6:99373381 | T | C | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.730-1794A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373381 | |||||||
| chr6:99373605 | C | A | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(136): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.730-2018G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373605 | |||||||
| chr6:99373701 | G | A | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(136): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.730-2114C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373701 | |||||||
| chr6:99373730 | G | T | 2 | a0004c0004t0003g0166 a0004c0004t0003g0167 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.730-2143C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373730 | |||||||
| chr6:99373749 | T | C | 9 | a0003c0003t0003g0075 a0003c0003t0003g0225 a0003c0003t0003g0226 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.730-2162A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373749 | |||||||
| chr6:99373762 | C | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(55): Show |
80 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.730-2175G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373762 | |||||||
| chr6:99373804 | C | A | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(136): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.729+2136G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373804 | |||||||
| chr6:99373809 | T | C | 86 | a0001c0001t0002g0285 a0002c0002t0001g0001 a0002c0002t0001g0004 others(83): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.729+2131A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373809 | |||||||
| chr6:99373887 | G | A | 4 | a0003c0003t0003g0225 a0003c0003t0003g0226 a0003c0003t0003g0227 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+2053C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99373887 | |||||||
| chr6:99374019 | A | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.729+1921T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374019 | |||||||
| chr6:99374033 | T | G | 1 | a0001c0001t0001g0009 | 4 | HG02080.hp1 NA18943.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+1907A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374033 | |||||||
| chr6:99374098 | C | T | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.729+1842G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374098 | |||||||
| chr6:99374122 | C | CA | 36 | a0001c0001t0001g0208 a0002c0002t0001g0090 a0002c0002t0001g0095 others(33): Show |
50 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.729+1817dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374122 | |||||||
| chr6:99374122 | C | CAA | 10 | a0002c0002t0001g0203 a0003c0003t0003g0075 a0003c0003t0003g0147 others(7): Show |
10 | HG00621.hp1 HG01192.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.729+1816_729+1817d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374122 | |||||||
| chr6:99374137 | A | AAT | 60 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0065 others(57): Show |
80 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.729+1802_729+1803i others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374137 | |||||||
| chr6:99374137 | A | AT | 16 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0033 others(13): Show |
19 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.729+1802_729+1803i others(3): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374137 | |||||||
| chr6:99374137 | A | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(58): Show |
83 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.729+1803T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374137 | |||||||
| chr6:99374140 | A | T | 2 | a0001c0001t0002g0306 a0001c0001t0002g0307 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.729+1800T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374140 | |||||||
| chr6:99374144 | T | A | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(136): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.729+1796A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374144 | |||||||
| chr6:99374190 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.729+1750G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374190 | |||||||
| chr6:99374355 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(94): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.729+1585A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374355 | |||||||
| chr6:99374405 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.729+1535C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374405 | |||||||
| chr6:99374633 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.729+1307T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374633 | |||||||
| chr6:99374740 | C | T | 31 | a0003c0003t0003g0003 a0003c0003t0003g0010 a0003c0003t0003g0018 others(28): Show |
45 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.729+1200G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374740 | |||||||
| chr6:99374951 | T | C | 9 | a0003c0003t0003g0189 a0003c0003t0003g0202 a0003c0003t0004g0238 others(6): Show |
9 | HG00621.hp1 NA18949.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+989A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374951 | |||||||
| chr6:99374986 | C | CT | 14 | a0001c0001t0001g0212 a0002c0002t0001g0012 a0002c0002t0001g0185 others(11): Show |
17 | HG00621.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.729+953dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374986 | |||||||
| chr6:99374986 | CT | C | 7 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0071 others(4): Show |
9 | HG02630.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.729+953delA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99374986 | |||||||
| chr6:99375022 | T | G | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.729+918A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375022 | |||||||
| chr6:99375114 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.729+826G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375114 | |||||||
| chr6:99375118 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+822G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375118 | |||||||
| chr6:99375215 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+725C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375215 | |||||||
| chr6:99375241 | T | C | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.729+699A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375241 | |||||||
| chr6:99375271 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+669T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375271 | |||||||
| chr6:99375319 | C | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+621G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375319 | |||||||
| chr6:99375351 | T | C | 1 | a0003c0003t0003g0189 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.729+589A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375351 | |||||||
| chr6:99375364 | C | T | 10 | a0002c0002t0001g0044 a0003c0003t0003g0189 a0003c0003t0003g0202 others(7): Show |
11 | HG00621.hp1 NA18942.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.729+576G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375364 | |||||||
| chr6:99375386 | C | CT | 6 | a0001c0001t0002g0047 a0001c0001t0002g0052 a0001c0001t0002g0270 others(3): Show |
8 | HG00639.hp1 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+553dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375386 | |||||||
| chr6:99375446 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+494G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375446 | |||||||
| chr6:99375479 | G | T | 85 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(82): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.729+461C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375479 | |||||||
| chr6:99375688 | A | G | 9 | a0003c0003t0003g0189 a0003c0003t0003g0202 a0003c0003t0004g0238 others(6): Show |
9 | HG00621.hp1 NA18949.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+252T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375688 | |||||||
| chr6:99375724 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.729+216A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375724 | |||||||
| chr6:99375815 | C | G | 17 | a0003c0003t0003g0003 a0003c0003t0003g0032 a0003c0003t0003g0041 others(14): Show |
26 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.729+125G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 5/6 | chr6 | 99375815 | |||||||
| chr6:99376347 | A | G | 17 | a0003c0003t0003g0003 a0003c0003t0003g0032 a0003c0003t0003g0041 others(14): Show |
26 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.487-165T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376347 | |||||||
| chr6:99376529 | A | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.487-347T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376529 | |||||||
| chr6:99376741 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(143): Show |
192 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.487-559A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376741 | |||||||
| chr6:99376850 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+536G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376850 | |||||||
| chr6:99376994 | A | ATG | 27 | a0001c0001t0002g0297 a0002c0002t0001g0181 a0002c0002t0001g0184 others(24): Show |
36 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.486+390_486+391dup others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376994 | |||||||
| chr6:99376994 | A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0205 others(6): Show |
19 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.486+384_486+391dup others(8): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376994 | |||||||
| chr6:99376994 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0021 | 3 | HG00280.hp1 HG00642.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.486+382_486+391dup others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376994 | |||||||
| chr6:99376994 | ATG | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(60): Show |
86 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.486+390_486+391del others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99376994 | |||||||
| chr6:99377124 | C | T | 1 | a0003c0003t0003g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.486+262G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377124 | |||||||
| chr6:99377159 | G | A | 1 | a0004c0004t0003g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486+227C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377159 | |||||||
| chr6:99377171 | G | A | 47 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(44): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.486+215C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377171 | |||||||
| chr6:99377192 | T | A | 9 | a0003c0003t0003g0189 a0003c0003t0003g0202 a0003c0003t0004g0238 others(6): Show |
9 | HG00621.hp1 NA18949.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+194A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377192 | |||||||
| chr6:99377272 | C | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+114G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377272 | |||||||
| chr6:99377349 | T | TC | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.486+36dupG | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377349 | |||||||
| chr6:99377351 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(143): Show |
192 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.486+35A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 4/6 | chr6 | 99377351 | |||||||
| chr6:99377580 | C | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-95G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377580 | |||||||
| chr6:99377598 | AT | A | 12 | a0002c0002t0001g0044 a0002c0002t0001g0175 a0002c0002t0001g0187 others(9): Show |
13 | HG00621.hp1 HG00673.hp1 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.387-114delA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377598 | |||||||
| chr6:99377599 | T | TA | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(143): Show |
192 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.387-115_387-114ins others(1): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377599 | |||||||
| chr6:99377668 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.387-183C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377668 | |||||||
| chr6:99377798 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.387-313C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377798 | |||||||
| chr6:99377977 | T | C | 85 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(82): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.387-492A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99377977 | |||||||
| chr6:99378105 | CATAT | C | 3 | a0001c0001t0002g0289 a0004c0004t0003g0070 a0004c0004t0003g0165 |
3 | HG01109.hp2 HG02273.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.387-624_387-621del others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(1): Show |
C | 5 | a0001c0001t0001g0083 a0001c0001t0002g0261 a0004c0004t0003g0022 others(2): Show |
6 | HG01981.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.387-628_387-621del others(8): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(3): Show |
C | 7 | a0001c0001t0002g0050 a0001c0001t0002g0278 a0004c0004t0003g0073 others(4): Show |
8 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-630_387-621del others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(5): Show |
C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0060 others(12): Show |
23 | HG00642.hp2 HG01081.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.387-632_387-621del others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(7): Show |
C | 23 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0063 others(20): Show |
25 | HG00621.hp1 HG01123.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.387-634_387-621del others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(9): Show |
C | 40 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0131 others(37): Show |
52 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.387-636_387-621del others(16): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(11): Show |
C | 9 | a0001c0001t0001g0062 a0001c0001t0001g0228 a0001c0001t0002g0266 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-638_387-621del others(18): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(13): Show |
C | 1 | a0001c0001t0002g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.387-640_387-621del others(20): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(15): Show |
C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0154 a0001c0001t0002g0273 |
3 | NA18940.hp2 NA18999.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.387-642_387-621del others(22): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(25): Show |
C | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.387-652_387-621del others(32): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(29): Show |
C | 4 | a0005c0005t0003g0059 a0005c0005t0003g0217 a0005c0005t0003g0218 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-656_387-621del others(36): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378105 | CATATATA others(31): Show |
C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.387-658_387-621del others(38): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378105 | |||||||
| chr6:99378110 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-625T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378110 | |||||||
| chr6:99378119 | TATATATA others(4): Show |
T | 1 | a0001c0001t0002g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.387-645_387-635del others(11): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378119 | |||||||
| chr6:99378130 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.387-645T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378130 | |||||||
| chr6:99378131 | TATATATA others(25): Show |
T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.387-678_387-647del others(32): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378131 | |||||||
| chr6:99378132 | A | T | 30 | a0002c0002t0002g0231 a0003c0003t0003g0003 a0003c0003t0003g0010 others(27): Show |
42 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.387-647T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378132 | |||||||
| chr6:99378133 | TATATATA others(21): Show |
T | 30 | a0002c0002t0002g0231 a0003c0003t0003g0003 a0003c0003t0003g0010 others(27): Show |
42 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.387-676_387-649del others(28): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378133 | |||||||
| chr6:99378134 | A | T | 6 | a0001c0001t0002g0286 a0002c0002t0001g0001 a0002c0002t0002g0007 others(3): Show |
7 | HG02083.hp1 HG02155.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-649T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378134 | |||||||
| chr6:99378135 | TATATATA others(19): Show |
T | 5 | a0002c0002t0001g0001 a0002c0002t0002g0007 a0003c0003t0003g0003 others(2): Show |
6 | HG02083.hp1 HG02155.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-676_387-651del others(26): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378135 | |||||||
| chr6:99378135 | TATATATA others(21): Show |
T | 1 | a0001c0001t0002g0286 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.387-678_387-651del others(28): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378135 | |||||||
| chr6:99378136 | A | T | 33 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(30): Show |
54 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.387-651T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378136 | |||||||
| chr6:99378137 | TATATATA others(16): Show |
T | 1 | a0002c0002t0002g0294 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.387-675_387-653del others(23): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378137 | |||||||
| chr6:99378137 | TATATATA others(17): Show |
T | 33 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(30): Show |
54 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.387-676_387-653del others(24): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378137 | |||||||
| chr6:99378138 | A | T | 22 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0013 others(19): Show |
32 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.387-653T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378138 | |||||||
| chr6:99378139 | TATATATA others(14): Show |
T | 1 | a0002c0002t0001g0001 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.387-675_387-655del others(21): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378139 | |||||||
| chr6:99378139 | TATATATA others(15): Show |
T | 23 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0013 others(20): Show |
33 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.387-676_387-655del others(22): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378139 | |||||||
| chr6:99378140 | A | T | 15 | a0001c0001t0001g0008 a0002c0002t0001g0001 a0002c0002t0001g0004 others(12): Show |
19 | HG00673.hp2 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.387-655T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378140 | |||||||
| chr6:99378141 | TATATATA others(13): Show |
T | 14 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0019 others(11): Show |
18 | HG00673.hp2 HG01256.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.387-676_387-657del others(20): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378141 | |||||||
| chr6:99378141 | TATATATA others(15): Show |
T | 1 | a0001c0001t0001g0008 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.387-678_387-657del others(22): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378141 | |||||||
| chr6:99378142 | A | T | 14 | a0001c0001t0001g0079 a0002c0002t0001g0090 a0002c0002t0001g0095 others(11): Show |
15 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.387-657T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378142 | |||||||
| chr6:99378143 | TATATATA others(11): Show |
T | 13 | a0002c0002t0001g0090 a0002c0002t0001g0095 a0002c0002t0001g0105 others(10): Show |
14 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.387-676_387-659del others(18): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378143 | |||||||
| chr6:99378144 | A | T | 6 | a0001c0001t0001g0109 a0002c0002t0001g0114 a0002c0002t0002g0014 others(3): Show |
6 | HG00280.hp2 HG00733.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-659T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378144 | |||||||
| chr6:99378144 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.387-673_387-660del others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378144 | |||||||
| chr6:99378145 | TATATATA others(9): Show |
T | 5 | a0002c0002t0001g0114 a0002c0002t0002g0014 a0002c0002t0002g0237 others(2): Show |
5 | HG00280.hp2 HG00733.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.387-676_387-661del others(16): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378145 | |||||||
| chr6:99378145 | TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0109 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.387-678_387-661del others(18): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378145 | |||||||
| chr6:99378146 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0190 others(2): Show |
5 | HG00323.hp1 HG03098.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-661T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378146 | |||||||
| chr6:99378147 | TATATATA others(7): Show |
T | 2 | a0002c0002t0002g0252 a0002c0002t0002g0255 |
2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.387-676_387-663del others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378147 | |||||||
| chr6:99378147 | TATATATA others(9): Show |
T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0190 |
3 | HG00323.hp1 NA18981.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.387-678_387-663del others(16): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378147 | |||||||
| chr6:99378148 | A | T | 1 | a0002c0002t0002g0249 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.387-663T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378148 | |||||||
| chr6:99378149 | TATATATA others(5): Show |
T | 1 | a0002c0002t0002g0249 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.387-676_387-665del others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378149 | |||||||
| chr6:99378149 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0117 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.387-678_387-665del others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378149 | |||||||
| chr6:99378150 | A | T | 1 | a0002c0002t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387-665T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378150 | |||||||
| chr6:99378151 | TATATATT others(3): Show |
T | 1 | a0002c0002t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387-676_387-667del others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378151 | |||||||
| chr6:99378152 | A | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0066 others(8): Show |
11 | HG01358.hp1 HG01433.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.387-667T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378152 | |||||||
| chr6:99378153 | TATATTTA others(3): Show |
T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0066 a0001c0001t0001g0097 others(4): Show |
7 | HG01358.hp1 HG01433.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-678_387-669del others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378153 | |||||||
| chr6:99378153 | TATATTTA others(7): Show |
T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.387-682_387-669del others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378153 | |||||||
| chr6:99378154 | A | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
8 | HG01928.hp2 HG02083.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-669T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378154 | |||||||
| chr6:99378155 | TATTTAGA others(1): Show |
T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
7 | HG01928.hp2 HG02083.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.387-678_387-671del others(8): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378155 | |||||||
| chr6:99378155 | TATTTAGA others(5): Show |
T | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.387-682_387-671del others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378155 | |||||||
| chr6:99378156 | A | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0025 others(10): Show |
14 | HG01261.hp1 HG01975.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.387-671T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378156 | |||||||
| chr6:99378156 | ATT | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(8): Show |
12 | HG00639.hp2 HG00741.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-673_387-672del others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378156 | |||||||
| chr6:99378157 | TTTAGAG | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0029 others(6): Show |
10 | HG01261.hp1 HG01975.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-678_387-673del others(6): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378157 | |||||||
| chr6:99378157 | TTTAGAGA others(3): Show |
T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0173 |
2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.387-682_387-673del others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378157 | |||||||
| chr6:99378158 | T | A | 19 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0025 others(16): Show |
21 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.387-673A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378158 | |||||||
| chr6:99378159 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.387-674A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378159 | |||||||
| chr6:99378159 | TAGAG | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(11): Show |
15 | HG00099.hp1 HG01255.hp1 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.387-678_387-675del others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378159 | |||||||
| chr6:99378160 | A | ATATATAT others(5): Show |
1 | a0002c0002t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.387-676_387-675ins others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378160 | |||||||
| chr6:99378160 | A | T | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.387-675T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378160 | |||||||
| chr6:99378161 | G | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(26): Show |
34 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.387-676C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378161 | |||||||
| chr6:99378162 | A | ATATATT | 4 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.387-678_387-677ins others(6): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378162 | |||||||
| chr6:99378162 | A | ATT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0038 others(2): Show |
5 | HG01256.hp1 HG01943.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-678_387-677ins others(2): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378162 | |||||||
| chr6:99378162 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(12): Show |
17 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.387-677T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378162 | |||||||
| chr6:99378163 | G | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(23): Show |
31 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.387-678C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378163 | |||||||
| chr6:99378221 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.387-736T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378221 | |||||||
| chr6:99378371 | G | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.387-886C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378371 | |||||||
| chr6:99378389 | A | G | 61 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(58): Show |
83 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.387-904T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378389 | |||||||
| chr6:99378441 | T | C | 1 | a0003c0003t0003g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.387-956A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378441 | |||||||
| chr6:99378514 | G | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-1029C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378514 | |||||||
| chr6:99378606 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.387-1121G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378606 | |||||||
| chr6:99378666 | G | A | 1 | a0003c0003t0003g0148 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.387-1181C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378666 | |||||||
| chr6:99378677 | G | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0011 others(81): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.387-1192C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378677 | |||||||
| chr6:99378765 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.387-1280C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378765 | |||||||
| chr6:99378886 | C | T | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(138): Show |
186 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.386+1303G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378886 | |||||||
| chr6:99378948 | C | CT | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(136): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.386+1240dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378948 | |||||||
| chr6:99378948 | CTT | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+1239_386+1240d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99378948 | |||||||
| chr6:99379025 | A | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0002c0002t0001g0179 |
4 | HG01074.hp2 HG01109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+1164T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379025 | |||||||
| chr6:99379044 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.386+1145A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379044 | |||||||
| chr6:99379072 | T | A | 1 | a0003c0003t0004g0243 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.386+1117A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379072 | |||||||
| chr6:99379121 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.386+1068G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379121 | |||||||
| chr6:99379161 | G | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.386+1028C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379161 | |||||||
| chr6:99379296 | T | G | 9 | a0003c0003t0003g0189 a0003c0003t0003g0202 a0003c0003t0004g0238 others(6): Show |
9 | HG00621.hp1 NA18949.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.386+893A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379296 | |||||||
| chr6:99379407 | T | C | 79 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0033 others(76): Show |
102 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.386+782A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379407 | |||||||
| chr6:99379438 | T | C | 225 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(222): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.386+751A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379438 | |||||||
| chr6:99379503 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0064 |
2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.386+686C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379503 | |||||||
| chr6:99379613 | G | C | 1 | a0001c0001t0002g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.386+576C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379613 | |||||||
| chr6:99379613 | G | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(137): Show |
185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.386+576C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379613 | |||||||
| chr6:99379696 | A | C | 1 | a0002c0002t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.386+493T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379696 | |||||||
| chr6:99379770 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
6 | NA18977.hp2 NA18989.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+419C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379770 | |||||||
| chr6:99379855 | C | CA | 12 | a0003c0003t0003g0067 a0003c0003t0003g0189 a0003c0003t0003g0202 others(9): Show |
12 | HG00621.hp1 HG02723.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+333dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 3/6 | chr6 | 99379855 | |||||||
| chr6:99380459 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-118G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380459 | |||||||
| chr6:99380484 | C | T | 2 | a0004c0004t0003g0166 a0004c0004t0003g0167 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.234-143G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380484 | |||||||
| chr6:99380527 | C | T | 4 | a0005c0005t0003g0059 a0005c0005t0003g0217 a0005c0005t0003g0218 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-186G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380527 | |||||||
| chr6:99380532 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.234-191C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380532 | |||||||
| chr6:99380685 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.234-344G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380685 | |||||||
| chr6:99380703 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234-362T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380703 | |||||||
| chr6:99380855 | A | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.234-514T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380855 | |||||||
| chr6:99380882 | C | T | 9 | a0003c0003t0003g0075 a0003c0003t0003g0225 a0003c0003t0003g0226 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.234-541G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380882 | |||||||
| chr6:99380886 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
5 | NA18977.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-545C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380886 | |||||||
| chr6:99380920 | AAAT | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-582_234-580del others(3): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99380920 | |||||||
| chr6:99381065 | G | A | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(56): Show |
81 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.234-724C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381065 | |||||||
| chr6:99381113 | A | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-772T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381113 | |||||||
| chr6:99381289 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-948T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381289 | |||||||
| chr6:99381302 | T | C | 1 | a0002c0002t0001g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.234-961A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381302 | |||||||
| chr6:99381362 | T | A | 31 | a0003c0003t0003g0003 a0003c0003t0003g0010 a0003c0003t0003g0018 others(28): Show |
45 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.234-1021A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381362 | |||||||
| chr6:99381381 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0104 |
3 | HG01891.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.234-1040A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381381 | |||||||
| chr6:99381457 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG01168.hp1 HG01169.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.234-1116C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381457 | |||||||
| chr6:99381576 | T | A | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(138): Show |
186 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.234-1235A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381576 | |||||||
| chr6:99381579 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.234-1238A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381579 | |||||||
| chr6:99381715 | C | T | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234-1374G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381715 | |||||||
| chr6:99381734 | T | G | 3 | a0002c0002t0001g0197 a0002c0002t0002g0007 a0002c0002t0002g0284 |
9 | HG00408.hp2 HG02040.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-1393A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381734 | |||||||
| chr6:99381890 | C | T | 1 | a0002c0002t0001g0180 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.234-1549G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381890 | |||||||
| chr6:99381925 | C | CA | 80 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0107 others(77): Show |
131 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.234-1585dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381925 | |||||||
| chr6:99381925 | C | CAA | 10 | a0002c0002t0001g0177 a0002c0002t0001g0188 a0002c0002t0002g0311 others(7): Show |
10 | HG00280.hp2 HG00621.hp1 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1586_234-1585d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381925 | |||||||
| chr6:99381925 | CA | C | 83 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0033 others(80): Show |
105 | HG00408.hp1 HG00639.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.234-1585delT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99381925 | |||||||
| chr6:99382016 | C | A | 1 | a0003c0003t0003g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.234-1675G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382016 | |||||||
| chr6:99382023 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.233+1675G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382023 | |||||||
| chr6:99382270 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
262 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.233+1428T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382270 | |||||||
| chr6:99382454 | T | A | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | NA18951.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.233+1244A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382454 | |||||||
| chr6:99382496 | C | T | 1 | a0002c0002t0001g0103 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.233+1202G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382496 | |||||||
| chr6:99382640 | G | A | 2 | a0002c0002t0001g0149 a0002c0002t0001g0158 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.233+1058C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382640 | |||||||
| chr6:99382674 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.233+1024G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382674 | |||||||
| chr6:99382682 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(124): Show |
166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.233+1016C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382682 | |||||||
| chr6:99382682 | G | C | 3 | a0003c0003t0003g0032 a0003c0003t0003g0087 a0003c0003t0004g0260 |
4 | NA18942.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1016C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382682 | |||||||
| chr6:99382705 | G | A | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(138): Show |
183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.233+993C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382705 | |||||||
| chr6:99382974 | G | GA | 164 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(161): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.233+723dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99382974 | |||||||
| chr6:99383026 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(295): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.233+672C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383026 | |||||||
| chr6:99383135 | AAAC | A | 6 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0071 others(3): Show |
8 | HG02630.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+560_233+562del others(3): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383135 | |||||||
| chr6:99383161 | C | G | 1 | a0004c0004t0003g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.233+537G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383161 | |||||||
| chr6:99383229 | A | C | 1 | a0003c0003t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233+469T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383229 | |||||||
| chr6:99383241 | A | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+457T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383241 | |||||||
| chr6:99383459 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.233+239C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383459 | |||||||
| chr6:99383618 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.233+80C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383618 | |||||||
| chr6:99383666 | G | A | 34 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0141 others(31): Show |
49 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.233+32C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 2/6 | chr6 | 99383666 | |||||||
| chr6:99383896 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.107-72C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99383896 | |||||||
| chr6:99383965 | A | G | 3 | a0005c0005t0003g0217 a0005c0005t0003g0218 a0005c0005t0003g0219 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.107-141T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99383965 | |||||||
| chr6:99384005 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.107-181T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384005 | |||||||
| chr6:99384010 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.107-186G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384010 | |||||||
| chr6:99384032 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.107-208G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384032 | |||||||
| chr6:99384033 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
6 | NA18949.hp1 NA18950.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-209C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384033 | |||||||
| chr6:99384046 | G | A | 1 | a0002c0002t0001g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.107-222C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384046 | |||||||
| chr6:99384058 | G | A | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-234C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384058 | |||||||
| chr6:99384075 | T | C | 1 | a0002c0002t0001g0197 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.107-251A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384075 | |||||||
| chr6:99384224 | A | G | 1 | a0002c0002t0002g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.107-400T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384224 | |||||||
| chr6:99384255 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.107-431C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384255 | |||||||
| chr6:99384512 | T | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(9): Show |
24 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.107-688A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384512 | |||||||
| chr6:99384668 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.107-844A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384668 | |||||||
| chr6:99384766 | T | C | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-942A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384766 | |||||||
| chr6:99384871 | G | A | 11 | a0001c0001t0001g0228 a0003c0003t0003g0225 a0003c0003t0003g0226 others(8): Show |
11 | HG01099.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-1047C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99384871 | |||||||
| chr6:99385089 | C | A | 1 | a0007c0009t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.107-1265G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385089 | |||||||
| chr6:99385089 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.107-1265G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385089 | |||||||
| chr6:99385097 | C | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0049 a0001c0001t0002g0055 others(23): Show |
34 | HG02015.hp1 HG02129.hp1 HG02165.hp2 others(31): Show |
intron_variant | MODIFIER | c.107-1273G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385097 | |||||||
| chr6:99385103 | T | C | 1 | a0002c0002t0002g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107-1279A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385103 | |||||||
| chr6:99385168 | A | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0060 others(10): Show |
15 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-1344T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385168 | |||||||
| chr6:99385203 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.107-1379A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385203 | |||||||
| chr6:99385264 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.107-1440C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385264 | |||||||
| chr6:99385542 | G | A | 1 | a0004c0004t0003g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-1718C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385542 | |||||||
| chr6:99385654 | C | A | 1 | a0003c0003t0003g0150 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107-1830G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385654 | |||||||
| chr6:99385694 | A | G | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-1870T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385694 | |||||||
| chr6:99385976 | CA | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(167): Show |
248 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.107-2153delT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385976 | |||||||
| chr6:99385986 | AAAAAAAA others(6): Show |
A | 1 | a0002c0002t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.107-2175_107-2163d others(15): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385986 | |||||||
| chr6:99385987 | AAAAAAAG others(5): Show |
A | 1 | a0002c0002t0001g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107-2175_107-2164d others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385987 | |||||||
| chr6:99385987 | AAAAAAAG others(12): Show |
A | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.107-2182_107-2164d others(21): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385987 | |||||||
| chr6:99385988 | AAAAAAGA others(11): Show |
A | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(66): Show |
94 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.107-2182_107-2165d others(20): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385988 | |||||||
| chr6:99385989 | AAAAAGAA others(10): Show |
A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0120 |
2 | HG01109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.107-2182_107-2166d others(19): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99385989 | |||||||
| chr6:99386043 | AATC | A | 155 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0168 others(152): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.107-2222_107-2220d others(5): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386043 | |||||||
| chr6:99386344 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(163): Show |
244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.107-2520A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386344 | |||||||
| chr6:99386496 | G | A | 9 | a0002c0002t0001g0013 a0002c0002t0001g0046 a0002c0002t0001g0056 others(6): Show |
13 | HG00323.hp2 HG00733.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-2672C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386496 | |||||||
| chr6:99386514 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.107-2690G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386514 | |||||||
| chr6:99386533 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107-2709T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386533 | |||||||
| chr6:99386959 | T | A | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-3135A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99386959 | |||||||
| chr6:99387049 | C | G | 1 | a0003c0003t0003g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107-3225G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387049 | |||||||
| chr6:99387053 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(164): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.107-3229G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387053 | |||||||
| chr6:99387131 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(175): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.107-3307A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387131 | |||||||
| chr6:99387246 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(175): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.107-3422A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387246 | |||||||
| chr6:99387265 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.107-3441T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387265 | |||||||
| chr6:99387305 | G | A | 1 | a0002c0002t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107-3481C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387305 | |||||||
| chr6:99387539 | T | C | 2 | a0001c0001t0002g0306 a0001c0001t0002g0307 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.107-3715A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387539 | |||||||
| chr6:99387595 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(174): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.107-3771G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387595 | |||||||
| chr6:99387731 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.107-3907A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387731 | |||||||
| chr6:99387846 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.107-4022A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387846 | |||||||
| chr6:99387935 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
87 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.107-4111G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387935 | |||||||
| chr6:99387936 | G | A | 2 | a0001c0001t0002g0247 a0002c0002t0002g0257 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.107-4112C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387936 | |||||||
| chr6:99387962 | C | T | 2 | a0003c0003t0003g0138 a0003c0003t0003g0152 |
2 | HG01123.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.107-4138G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99387962 | |||||||
| chr6:99388056 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.107-4232G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388056 | |||||||
| chr6:99388095 | C | T | 2 | a0002c0002t0001g0019 a0002c0002t0001g0177 |
4 | NA19005.hp2 NA19056.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-4271G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388095 | |||||||
| chr6:99388212 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0060 others(10): Show |
15 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-4388G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388212 | |||||||
| chr6:99388301 | T | C | 1 | a0002c0002t0001g0199 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.107-4477A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388301 | |||||||
| chr6:99388492 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.107-4668T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388492 | |||||||
| chr6:99388506 | C | CT | 232 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(229): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.107-4683dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388506 | |||||||
| chr6:99388506 | C | CTT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-4684_107-4683d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388506 | |||||||
| chr6:99388555 | A | G | 1 | a0003c0003t0004g0269 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.107-4731T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388555 | |||||||
| chr6:99388676 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-4852G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388676 | |||||||
| chr6:99388720 | A | C | 297 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(294): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.107-4896T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388720 | |||||||
| chr6:99388724 | T | C | 1 | a0002c0002t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107-4900A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388724 | |||||||
| chr6:99388777 | G | A | 4 | a0001c0001t0001g0113 a0002c0002t0001g0114 a0002c0002t0001g0126 others(1): Show |
4 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-4953C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388777 | |||||||
| chr6:99388815 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107-4991A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388815 | |||||||
| chr6:99388835 | C | T | 1 | a0003c0003t0003g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.107-5011G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388835 | |||||||
| chr6:99388882 | T | C | 119 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(116): Show |
161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.107-5058A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388882 | |||||||
| chr6:99388890 | C | T | 2 | a0001c0001t0001g0078 a0004c0004t0003g0076 |
2 | HG00735.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-5066G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388890 | |||||||
| chr6:99388891 | G | GCA | 5 | a0001c0001t0001g0171 a0002c0002t0001g0013 a0002c0002t0001g0203 others(2): Show |
8 | HG00323.hp2 HG01106.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-5069_107-5068d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCA | G | 26 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0063 others(23): Show |
33 | HG00099.hp2 HG01069.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.107-5069_107-5068d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACA | G | 82 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0212 others(79): Show |
113 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.107-5071_107-5068d others(6): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACA | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
60 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.107-5073_107-5068d others(8): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACAC others(1): Show |
G | 62 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(59): Show |
84 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.107-5075_107-5068d others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.107-5077_107-5068d others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACAC others(5): Show |
G | 5 | a0001c0001t0001g0169 a0002c0002t0001g0172 a0004c0004t0003g0214 others(2): Show |
5 | HG01099.hp2 HG01891.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-5079_107-5068d others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-5081_107-5068d others(16): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388891 | GCACACAC others(9): Show |
G | 2 | a0001c0001t0001g0089 a0002c0002t0002g0253 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.107-5083_107-5068d others(18): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388891 | |||||||
| chr6:99388899 | A | G | 15 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0036 others(12): Show |
18 | HG01433.hp1 HG02109.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.107-5075T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388899 | |||||||
| chr6:99388901 | A | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(52): Show |
77 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.107-5077T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388901 | |||||||
| chr6:99388903 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.107-5079T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388903 | |||||||
| chr6:99388907 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-5083T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388907 | |||||||
| chr6:99388909 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-5085T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388909 | |||||||
| chr6:99388919 | A | C | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-5095T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388919 | |||||||
| chr6:99388921 | ACACACAC others(7): Show |
A | 1 | a0003c0003t0003g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.107-5111_107-5098d others(16): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388921 | |||||||
| chr6:99388923 | ACACACAC others(5): Show |
A | 24 | a0001c0001t0001g0065 a0001c0001t0001g0141 a0001c0001t0001g0142 others(21): Show |
32 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.107-5111_107-5100d others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388923 | |||||||
| chr6:99388925 | ACACACAC others(3): Show |
A | 11 | a0001c0001t0001g0040 a0002c0002t0001g0039 a0002c0002t0001g0149 others(8): Show |
17 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.107-5111_107-5102d others(12): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388925 | |||||||
| chr6:99388927 | A | C | 1 | a0005c0005t0003g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-5103T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388927 | |||||||
| chr6:99388929 | A | C | 3 | a0005c0005t0003g0217 a0005c0005t0003g0218 a0005c0005t0003g0219 |
3 | HG02258.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.107-5105T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388929 | |||||||
| chr6:99388930 | CACA | C | 3 | a0001c0001t0002g0235 a0003c0003t0004g0250 a0003c0003t0004g0251 |
3 | HG00621.hp1 NA18978.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.107-5109_107-5107d others(5): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388930 | |||||||
| chr6:99388931 | A | C | 3 | a0001c0001t0002g0005 a0002c0002t0001g0001 a0004c0004t0003g0221 |
4 | HG03704.hp1 NA18957.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-5107T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388931 | |||||||
| chr6:99388933 | A | ACC | 4 | a0001c0001t0001g0194 a0002c0002t0001g0001 a0002c0002t0001g0175 others(1): Show |
5 | HG00673.hp1 HG02155.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-5111_107-5110d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388933 | |||||||
| chr6:99388933 | A | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(134): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.107-5109T>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388933 | |||||||
| chr6:99388967 | T | C | 1 | a0001c0001t0002g0295 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.106+5107A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99388967 | |||||||
| chr6:99389078 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0208 others(4): Show |
17 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+4996C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389078 | |||||||
| chr6:99389208 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(174): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.106+4866A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389208 | |||||||
| chr6:99389354 | A | G | 1 | a0002c0002t0001g0176 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.106+4720T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389354 | |||||||
| chr6:99389404 | C | T | 11 | a0001c0001t0001g0228 a0003c0003t0003g0225 a0003c0003t0003g0226 others(8): Show |
11 | HG01099.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+4670G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389404 | |||||||
| chr6:99389481 | T | TA | 4 | a0001c0001t0001g0212 a0004c0004t0003g0221 a0004c0004t0003g0222 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+4592dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389481 | |||||||
| chr6:99389555 | C | T | 4 | a0001c0001t0001g0212 a0004c0004t0003g0221 a0004c0004t0003g0222 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+4519G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99389555 | |||||||
| chr6:99390131 | G | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
10 | HG02015.hp1 NA18945.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+3943C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390131 | |||||||
| chr6:99390326 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.106+3748T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390326 | |||||||
| chr6:99390333 | AC | A | 11 | a0001c0001t0001g0228 a0003c0003t0003g0225 a0003c0003t0003g0226 others(8): Show |
11 | HG01099.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+3740delG | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390333 | |||||||
| chr6:99390334 | CT | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.106+3739delA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390334 | |||||||
| chr6:99390335 | T | A | 11 | a0001c0001t0001g0228 a0003c0003t0003g0225 a0003c0003t0003g0226 others(8): Show |
11 | HG01099.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+3739A>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390335 | |||||||
| chr6:99390360 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0084 |
4 | HG02258.hp1 HG02622.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3714C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390360 | |||||||
| chr6:99390379 | G | T | 144 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0168 others(141): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.106+3695C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390379 | |||||||
| chr6:99390459 | G | A | 297 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(294): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.106+3615C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390459 | |||||||
| chr6:99390721 | G | T | 1 | a0002c0002t0001g0175 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.106+3353C>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390721 | |||||||
| chr6:99390805 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.106+3269G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390805 | |||||||
| chr6:99390936 | T | C | 5 | a0001c0001t0001g0228 a0003c0003t0003g0225 a0003c0003t0003g0226 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3138A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390936 | |||||||
| chr6:99390941 | T | C | 1 | a0001c0001t0002g0263 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.106+3133A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99390941 | |||||||
| chr6:99391075 | T | TTTTA | 112 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0040 others(109): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.106+2995_106+2998d others(6): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391075 | |||||||
| chr6:99391075 | T | TTTTATTT others(1): Show |
39 | a0001c0001t0001g0065 a0001c0001t0001g0154 a0001c0001t0002g0055 others(36): Show |
46 | HG00280.hp2 HG00408.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.106+2991_106+2998d others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391075 | |||||||
| chr6:99391075 | TTTTATTT others(1): Show |
T | 10 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 others(7): Show |
10 | HG01496.hp2 HG01952.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+2991_106+2998d others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391075 | |||||||
| chr6:99391075 | TTTTATTT others(5): Show |
T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
35 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+2987_106+2998d others(14): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391075 | |||||||
| chr6:99391090 | T | TATTGATT others(1): Show |
5 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0118 others(2): Show |
5 | HG00323.hp1 HG01928.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+2983_106+2984i others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391090 | |||||||
| chr6:99391094 | T | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG00323.hp1 HG01928.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2980A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391094 | |||||||
| chr6:99391094 | T | TATTGATT others(1): Show |
41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(38): Show |
59 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.106+2979_106+2980i others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391094 | |||||||
| chr6:99391098 | T | G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(39): Show |
59 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.106+2976A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391098 | |||||||
| chr6:99391098 | T | TATTGATT others(1): Show |
23 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0030 others(20): Show |
29 | HG00099.hp1 HG01109.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.106+2975_106+2976i others(10): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391098 | |||||||
| chr6:99391102 | T | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0066 others(14): Show |
20 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+2972A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391102 | |||||||
| chr6:99391106 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00639.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.106+2968A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391106 | |||||||
| chr6:99391107 | A | G | 1 | a0002c0002t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.106+2967T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391107 | |||||||
| chr6:99391206 | C | G | 1 | a0002c0002t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.106+2868G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391206 | |||||||
| chr6:99391230 | C | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0258 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.106+2844G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391230 | |||||||
| chr6:99391273 | A | AT | 67 | a0001c0001t0001g0212 a0001c0001t0002g0005 a0001c0001t0002g0006 others(64): Show |
93 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.106+2800dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391273 | |||||||
| chr6:99391273 | A | ATT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2799_106+2800d others(4): Show |
COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391273 | |||||||
| chr6:99391388 | G | A | 3 | a0004c0004t0003g0221 a0004c0004t0003g0222 a0004c0004t0003g0223 |
3 | HG02895.hp1 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+2686C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391388 | |||||||
| chr6:99391503 | T | C | 69 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0047 others(66): Show |
95 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.106+2571A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391503 | |||||||
| chr6:99391603 | G | GC | 296 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(293): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.106+2470dupG | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391603 | |||||||
| chr6:99391611 | G | A | 5 | a0004c0004t0003g0163 a0004c0004t0003g0164 a0004c0004t0003g0165 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+2463C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391611 | |||||||
| chr6:99391725 | C | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.106+2349G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391725 | |||||||
| chr6:99391756 | T | C | 5 | a0004c0004t0003g0163 a0004c0004t0003g0164 a0004c0004t0003g0165 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+2318A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391756 | |||||||
| chr6:99391763 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.106+2311G>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391763 | |||||||
| chr6:99391775 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.106+2299C>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391775 | |||||||
| chr6:99391778 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(293): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.106+2296A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391778 | |||||||
| chr6:99391998 | C | CA | 17 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
30 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+2075dupT | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99391998 | |||||||
| chr6:99392316 | C | A | 34 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0141 others(31): Show |
49 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.106+1758G>T | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392316 | |||||||
| chr6:99392412 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.106+1662A>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392412 | |||||||
| chr6:99392430 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.106+1644G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392430 | |||||||
| chr6:99392451 | A | G | 1 | a0001c0001t0002g0047 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.106+1623T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392451 | |||||||
| chr6:99392629 | C | CT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
33 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.106+1444dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392629 | |||||||
| chr6:99392777 | C | T | 1 | a0007c0009t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106+1297G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99392777 | |||||||
| chr6:99393043 | C | T | 143 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(140): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.106+1031G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393043 | |||||||
| chr6:99393133 | A | G | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | NA19002.hp1 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.106+941T>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393133 | |||||||
| chr6:99393192 | C | CT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG01891.hp1 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+881dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393192 | |||||||
| chr6:99393192 | CT | C | 11 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+881delA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393192 | |||||||
| chr6:99393730 | G | GT | 5 | a0004c0004t0003g0163 a0004c0004t0003g0164 a0004c0004t0003g0165 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+343dupA | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393730 | |||||||
| chr6:99393934 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.106+140C>G | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99393934 | |||||||
| chr6:99394031 | T | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(172): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.106+43A>C | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99394031 | |||||||
| chr6:99394036 | A | T | 1 | a0002c0002t0001g0056 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.106+38T>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99394036 | |||||||
| chr6:99394056 | C | T | 1 | a0002c0002t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.106+18G>A | COQ3 | ENSG00000132423.12 | transcript | ENST00000254759.8 | protein_coding | 1/6 | chr6 | 99394056 |