Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 170712 |
|---|---|
| ensemblid | ENSG00000170516.17 |
| hgncid | 24381 |
| symbol | COX7B2 |
| name | cytochrome c oxidase subunit 7B2 |
| refseq_nuc | NM_130902.3 |
| refseq_prot | NP_570972.2 |
| ensembl_nuc | ENST00000355591.8 |
| ensembl_prot | ENSP00000347799.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 46734827 |
| end | 46909245 |
| strand | - |
| ver | v1.2 |
| region | chr4:46734827-46909245 |
| region5000 | chr4:46729827-46914245 |
| regionname0 | COX7B2_chr4_46734827_46909245 |
| regionname5000 | COX7B2_chr4_46729827_46914245 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001 | 1/1 | 81 | 298 | 73 | 52 | 131 | 10 | 30 | 99 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0002 | 0/0 | 81 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 246 | 298 | 73 | 52 | 131 | 10 | 30 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| c0002 | 0/0 | 262 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| c0003 | 0/0 | 246 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 311 | 163 | 52 | 31 | 53 | 5 | 21 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0002 | 0/0 | 311 | 66 | 15 | 9 | 34 | 4 | 4 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0003 | 0/1 | 311 | 61 | 4 | 12 | 40 | 0 | 4 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0004 | 0/0 | 311 | 4 | 1 | 0 | 1 | 1 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0005 | 0/0 | 311 | 3 | 0 | 0 | 3 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0006 | 0/0 | 311 | 2 | 2 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| t0007 | 0/0 | 311 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0002 | 0/0 | 262 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001 | 1/1 | 246 | 298 | 73 | 52 | 131 | 10 | 30 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0002c0003 | 0/0 | 246 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0002t0003 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0001 | 1/0 | 556 | 162 | 51 | 31 | 53 | 5 | 21 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0002 | 0/0 | 556 | 66 | 15 | 9 | 34 | 4 | 4 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0003 | 0/1 | 556 | 60 | 4 | 12 | 39 | 0 | 4 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0004 | 0/0 | 556 | 4 | 1 | 0 | 1 | 1 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0005 | 0/0 | 556 | 3 | 0 | 0 | 3 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0006 | 0/0 | 556 | 2 | 2 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0001c0001t0007 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| a0002c0003t0001 | 0/0 | 556 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | copy fasta | chr4 | 46729827 | 46914245 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| a0002c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0035 | EUR | GBR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | FIN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CDX | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CDX | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0078 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | BEB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | STU | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | CHB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18972 | hp2 | a0000 | c0002 | t0003 | g0233 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19082 | hp2 | a0001 | c0001 | t0007 | g0239 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ASW | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | GIH | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | USA | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | USA | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0265 | REF | REF | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0135 | REF | REF | COX7B2_chr4_46729827_46914245 | COX7B2 | chr4 | 46729827 | 46914245 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:46734988
|
G | GGGATAGG others(9): Show |
1 | a0000 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.189_204dupAGAATGGA others(8): Show |
p.Pro69fs | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 3/3 | 394/556 | 204/246 | 68/81 | chr4 | 46734988 | ||
| chr4:46735023
|
G | A | 1 | a0002 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.170C>T | p.Thr57Ile | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 3/3 | 360/556 | 170/246 | 57/81 | chr4 | 46735023 |
| 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 |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:46734836
|
A | T | 4 | a0000c0002t0003a0001c0001t0003a0001c0001t0004others(1): Show | 66 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*111T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 3/3 | 111 | chr4 | 46734836 | |||||
| chr4:46735221
|
G | A | 1 | a0001c0001t0007 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 3/3 | 29 | chr4 | 46735221 | |||||
| chr4:46844999
|
T | C | 1 | a0001c0001t0006 | 2 | HG02622.hp1 HG02647.hp1 |
5_prime_UTR_variant | MODIFIER | c.-89A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/3 | 109807 | chr4 | 46844999 | |||||
| chr4:46909192
|
C | T | 2 | a0001c0001t0002a0001c0001t0004 | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
5_prime_UTR_variant | MODIFIER | c.-137G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/3 | 174000 | chr4 | 46909192 | |||||
| chr4:46909210
|
C | T | 1 | a0001c0001t0005 | 3 | NA18945.hp2 NA19003.hp2 NA19066.hp2 |
5_prime_UTR_variant | MODIFIER | c.-155G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/3 | 174018 | chr4 | 46909210 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:46735372
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0138others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-131A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735372 | ||||||
| chr4:46735503
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-262G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735503 | ||||||
| chr4:46735520
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-49-279T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735520 | ||||||
| chr4:46735642
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0294 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-49-401G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735642 | ||||||
| chr4:46735813
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-572T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735813 | ||||||
| chr4:46735939
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-698A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46735939 | ||||||
| chr4:46736073
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-832G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736073 | ||||||
| chr4:46736090
|
C | A | 61 | a0000c0002t0003g0233a0001c0001t0003g0003a0001c0001t0003g0084others(58): Show | 62 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-49-849G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736090 | ||||||
| chr4:46736142
|
A | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0138others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-901T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736142 | ||||||
| chr4:46736396
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-1155T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736396 | ||||||
| chr4:46736453
|
A | AT | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0064others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-1213dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736453 | ||||||
| chr4:46736733
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-49-1492G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736733 | ||||||
| chr4:46736910
|
T | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0109others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49-1669A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736910 | ||||||
| chr4:46736980
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-1739C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46736980 | ||||||
| chr4:46737074
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-1833C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737074 | ||||||
| chr4:46737265
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49-2024G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737265 | ||||||
| chr4:46737317
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2076C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737317 | ||||||
| chr4:46737454
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-49-2213T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737454 | ||||||
| chr4:46737535
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2294A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737535 | ||||||
| chr4:46737571
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2330C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737571 | ||||||
| chr4:46737764
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-49-2523T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737764 | ||||||
| chr4:46737945
|
C | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18966.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-49-2704G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46737945 | ||||||
| chr4:46738018
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0282 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-49-2777T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738018 | ||||||
| chr4:46738087
|
G | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-2846C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738087 | ||||||
| chr4:46738154
|
A | C | 1 | a0001c0001t0003g0235 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-49-2913T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738154 | ||||||
| chr4:46738232
|
T | A | 1 | a0001c0001t0003g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-49-2991A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738232 | ||||||
| chr4:46738615
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-3374T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738615 | ||||||
| chr4:46738657
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-3416T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738657 | ||||||
| chr4:46738702
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-49-3461C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738702 | ||||||
| chr4:46738786
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-3545C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738786 | ||||||
| chr4:46738862
|
A | C | 1 | a0001c0001t0003g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-49-3621T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46738862 | ||||||
| chr4:46739137
|
C | T | 1 | a0001c0001t0003g0261 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-49-3896G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739137 | ||||||
| chr4:46739180
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0045 | 2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-49-3939C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739180 | ||||||
| chr4:46739312
|
A | T | 2 | a0001c0001t0003g0111a0001c0001t0003g0151 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-49-4071T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739312 | ||||||
| chr4:46739343
|
C | A | 34 | a0001c0001t0001g0092a0001c0001t0001g0118a0001c0001t0001g0123others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.-49-4102G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739343 | ||||||
| chr4:46739343
|
C | CCAAAA | 7 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0138others(4): Show | 7 | HG01167.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-4107_-49-4103d others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739343 | ||||||
| chr4:46739343
|
CCAAAA | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(2): Show | 5 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-4107_-49-4103d others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739343 | ||||||
| chr4:46739348
|
A | C | 3 | a0001c0001t0001g0142a0001c0001t0007g0239a0002c0003t0001g0078 | 3 | HG02572.hp2 HG03130.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-49-4107T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739348 | ||||||
| chr4:46739350
|
A | C | 1 | a0001c0001t0002g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-49-4109T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739350 | ||||||
| chr4:46739416
|
T | C | 166 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(163): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-49-4175A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739416 | ||||||
| chr4:46739531
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-4290A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739531 | ||||||
| chr4:46739559
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-4318G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739559 | ||||||
| chr4:46739634
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0052 | 4 | NA18955.hp1 NA19011.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-4393A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739634 | ||||||
| chr4:46739703
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-4462T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739703 | ||||||
| chr4:46739798
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-49-4557A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46739798 | ||||||
| chr4:46740103
|
C | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0138others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-4862G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740103 | ||||||
| chr4:46740125
|
T | C | 2 | a0001c0001t0003g0242a0001c0001t0003g0271 | 2 | HG01358.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-49-4884A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740125 | ||||||
| chr4:46740254
|
CAT | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0195a0001c0001t0001g0212 | 3 | NA18950.hp1 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-49-5015_-49-5014d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740254 | ||||||
| chr4:46740404
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-5163C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740404 | ||||||
| chr4:46740409
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0158a0001c0001t0001g0216others(2): Show | 5 | HG01256.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-5168T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740409 | ||||||
| chr4:46740410
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-49-5169A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740410 | ||||||
| chr4:46740465
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49-5224A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740465 | ||||||
| chr4:46740474
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-5233T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740474 | ||||||
| chr4:46740632
|
T | C | 60 | a0000c0002t0003g0233a0001c0001t0003g0003a0001c0001t0003g0096others(57): Show | 61 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-49-5391A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740632 | ||||||
| chr4:46740756
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-5515G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740756 | ||||||
| chr4:46740789
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49-5548A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740789 | ||||||
| chr4:46740953
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-5712C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740953 | ||||||
| chr4:46740967
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-49-5726G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46740967 | ||||||
| chr4:46741012
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0282 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-49-5771A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741012 | ||||||
| chr4:46741144
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-5903C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741144 | ||||||
| chr4:46741194
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-5953G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741194 | ||||||
| chr4:46741301
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-49-6060A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741301 | ||||||
| chr4:46741547
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-6306G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741547 | ||||||
| chr4:46741573
|
A | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-6332T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741573 | ||||||
| chr4:46741586
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-6345A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741586 | ||||||
| chr4:46741788
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-49-6547A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741788 | ||||||
| chr4:46741845
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-6604T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741845 | ||||||
| chr4:46741962
|
A | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-6721T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741962 | ||||||
| chr4:46741977
|
T | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-6736A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741977 | ||||||
| chr4:46741981
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-49-6740G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46741981 | ||||||
| chr4:46742103
|
G | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-6862C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742103 | ||||||
| chr4:46742306
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7065T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742306 | ||||||
| chr4:46742330
|
TA | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7090delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742330 | ||||||
| chr4:46742384
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7143T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742384 | ||||||
| chr4:46742434
|
T | A | 2 | a0001c0001t0004g0008a0001c0001t0004g0035 | 2 | HG00140.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-49-7193A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742434 | ||||||
| chr4:46742482
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49-7241G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742482 | ||||||
| chr4:46742526
|
C | T | 20 | a0001c0001t0001g0092a0001c0001t0001g0118a0001c0001t0001g0123others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-49-7285G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742526 | ||||||
| chr4:46742527
|
G | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0282 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-49-7286C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742527 | ||||||
| chr4:46742820
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7579C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742820 | ||||||
| chr4:46742825
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7584C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46742825 | ||||||
| chr4:46743196
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7955A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743196 | ||||||
| chr4:46743227
|
T | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0138others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-7986A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743227 | ||||||
| chr4:46743402
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-8161G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743402 | ||||||
| chr4:46743428
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-8187A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743428 | ||||||
| chr4:46743606
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-8365G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743606 | ||||||
| chr4:46743671
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-8430T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743671 | ||||||
| chr4:46743693
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG02970.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-49-8452C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743693 | ||||||
| chr4:46743710
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-8469A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743710 | ||||||
| chr4:46743780
|
AT | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-8540delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743780 | ||||||
| chr4:46743886
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-8645A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46743886 | ||||||
| chr4:46744141
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-8900G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744141 | ||||||
| chr4:46744203
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-8962A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744203 | ||||||
| chr4:46744203
|
T | G | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-8962A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744203 | ||||||
| chr4:46744364
|
C | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0297 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49-9123G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744364 | ||||||
| chr4:46744516
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-9275A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744516 | ||||||
| chr4:46744634
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-9393C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744634 | ||||||
| chr4:46744674
|
T | C | 5 | a0001c0001t0003g0255a0001c0001t0003g0261a0001c0001t0003g0263others(2): Show | 5 | HG01070.hp2 HG01934.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-9433A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744674 | ||||||
| chr4:46744738
|
A | AT | 23 | a0001c0001t0001g0081a0001c0001t0001g0095a0001c0001t0001g0104others(20): Show | 23 | HG01175.hp1 HG01346.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-49-9498dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744738 | ||||||
| chr4:46744738
|
A | ATTTT | 45 | a0000c0002t0003g0233a0001c0001t0001g0249a0001c0001t0001g0250others(42): Show | 45 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-49-9501_-49-9498d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744738 | ||||||
| chr4:46744738
|
A | ATTTTT | 10 | a0001c0001t0003g0107a0001c0001t0003g0144a0001c0001t0003g0148others(7): Show | 10 | HG01109.hp2 HG01358.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-9502_-49-9498d others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744738 | ||||||
| chr4:46744758
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-49-9517A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744758 | ||||||
| chr4:46744792
|
T | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-9551A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744792 | ||||||
| chr4:46744804
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0002g0069 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-49-9563C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744804 | ||||||
| chr4:46744870
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49-9629G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744870 | ||||||
| chr4:46744896
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-9655T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744896 | ||||||
| chr4:46744913
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49-9672C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744913 | ||||||
| chr4:46744935
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-9694A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46744935 | ||||||
| chr4:46745077
|
T | C | 125 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(122): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49-9836A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745077 | ||||||
| chr4:46745154
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-9913G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745154 | ||||||
| chr4:46745292
|
C | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-10051G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745292 | ||||||
| chr4:46745635
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-10394T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745635 | ||||||
| chr4:46745930
|
T | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-10689A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745930 | ||||||
| chr4:46745965
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-49-10724G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745965 | ||||||
| chr4:46745995
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-10754T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46745995 | ||||||
| chr4:46746071
|
A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0073 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-49-10830T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746071 | ||||||
| chr4:46746084
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-49-10843G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746084 | ||||||
| chr4:46746098
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-10857T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746098 | ||||||
| chr4:46746275
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-11034C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746275 | ||||||
| chr4:46746351
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-11110A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746351 | ||||||
| chr4:46746526
|
G | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-11285C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746526 | ||||||
| chr4:46746551
|
C | CAA | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-11311_-49-1131 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46746551 | ||||||
| chr4:46747120
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-11879C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747120 | ||||||
| chr4:46747132
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-11891A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747132 | ||||||
| chr4:46747161
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-49-11920C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747161 | ||||||
| chr4:46747269
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-49-12028A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747269 | ||||||
| chr4:46747274
|
A | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12033T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747274 | ||||||
| chr4:46747280
|
C | CTATTT | 11 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG01106.hp1 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-12044_-49-1204 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747280 | ||||||
| chr4:46747298
|
T | TTTTATTT others(7): Show |
58 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-49-12071_-49-1205 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747298 | ||||||
| chr4:46747298
|
T | TTTTATTT others(12): Show |
58 | a0000c0002t0003g0233a0001c0001t0001g0154a0001c0001t0001g0157others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-12058_-49-1205 others(23): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747298 | ||||||
| chr4:46747298
|
T | TTTTATTT others(17): Show |
5 | a0001c0001t0001g0282a0001c0001t0003g0225a0001c0001t0003g0244others(2): Show | 5 | HG01261.hp2 HG03209.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-12058_-49-1205 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747298 | ||||||
| chr4:46747346
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-49-12105G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747346 | ||||||
| chr4:46747364
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12123A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747364 | ||||||
| chr4:46747372
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49-12131G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747372 | ||||||
| chr4:46747373
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-12132C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747373 | ||||||
| chr4:46747443
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12202T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747443 | ||||||
| chr4:46747476
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12235C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747476 | ||||||
| chr4:46747485
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12244T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747485 | ||||||
| chr4:46747510
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-12269C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747510 | ||||||
| chr4:46747530
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12289A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747530 | ||||||
| chr4:46747595
|
G | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12354C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747595 | ||||||
| chr4:46747598
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-49-12357C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747598 | ||||||
| chr4:46747606
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-49-12365G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747606 | ||||||
| chr4:46747609
|
C | A | 2 | a0001c0001t0003g0234a0001c0001t0003g0277 | 2 | HG02071.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-49-12368G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747609 | ||||||
| chr4:46747632
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12391G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747632 | ||||||
| chr4:46747698
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-49-12457T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747698 | ||||||
| chr4:46747780
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12539A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747780 | ||||||
| chr4:46747871
|
TTTAACGT others(134): Show |
T | 7 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0002g0012others(4): Show | 7 | HG00544.hp1 HG03490.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-12771_-49-1263 others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747871 | ||||||
| chr4:46747957
|
A | G | 2 | a0001c0001t0003g0225a0001c0001t0003g0229 | 2 | NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-49-12716T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46747957 | ||||||
| chr4:46748002
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-12761T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748002 | ||||||
| chr4:46748013
|
A | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0002g0012others(4): Show | 7 | HG00544.hp1 HG03490.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-12772T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748013 | ||||||
| chr4:46748044
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-12803T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748044 | ||||||
| chr4:46748049
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12808C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748049 | ||||||
| chr4:46748080
|
C | CA | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-12840dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748080 | ||||||
| chr4:46748175
|
G | C | 1 | a0001c0001t0002g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-49-12934C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748175 | ||||||
| chr4:46748215
|
T | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0141 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-12974A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748215 | ||||||
| chr4:46748316
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(17): Show | 22 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-49-13075G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748316 | ||||||
| chr4:46748510
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-13269G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748510 | ||||||
| chr4:46748624
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-13383G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748624 | ||||||
| chr4:46748696
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-13455T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748696 | ||||||
| chr4:46748706
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-13465A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748706 | ||||||
| chr4:46748919
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-13678G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748919 | ||||||
| chr4:46748960
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-13719T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46748960 | ||||||
| chr4:46749086
|
A | C | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-49-13845T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749086 | ||||||
| chr4:46749200
|
T | C | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-13959A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749200 | ||||||
| chr4:46749266
|
C | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14025G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749266 | ||||||
| chr4:46749332
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-14091C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749332 | ||||||
| chr4:46749344
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0197 | 2 | NA18995.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-49-14103T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749344 | ||||||
| chr4:46749488
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49-14247A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749488 | ||||||
| chr4:46749524
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14283A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749524 | ||||||
| chr4:46749528
|
G | T | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-14287C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749528 | ||||||
| chr4:46749589
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14348C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749589 | ||||||
| chr4:46749596
|
T | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14355A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749596 | ||||||
| chr4:46749600
|
T | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14359A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749600 | ||||||
| chr4:46749667
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-14426A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749667 | ||||||
| chr4:46749719
|
C | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-14478G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749719 | ||||||
| chr4:46749794
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14553T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749794 | ||||||
| chr4:46749801
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14560G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749801 | ||||||
| chr4:46749947
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-49-14706T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749947 | ||||||
| chr4:46749967
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-14726A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749967 | ||||||
| chr4:46749996
|
C | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-14755G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46749996 | ||||||
| chr4:46750144
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-14903A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750144 | ||||||
| chr4:46750195
|
T | TAC | 20 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0088others(17): Show | 20 | HG00621.hp1 HG01516.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-14956_-49-1495 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACAC | 51 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0090others(48): Show | 52 | HG00140.hp2 HG00423.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-49-14958_-49-1495 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACAC | 51 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0087others(48): Show | 51 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-49-14960_-49-1495 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(1): Show |
32 | a0001c0001t0001g0092a0001c0001t0001g0136a0001c0001t0001g0147others(29): Show | 32 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.-49-14962_-49-1495 others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(3): Show |
24 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0161others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-14964_-49-1495 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(5): Show |
5 | a0001c0001t0001g0216a0001c0001t0002g0019a0001c0001t0002g0029others(2): Show | 5 | HG00544.hp1 HG01257.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-14966_-49-1495 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(7): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0002g0040others(2): Show | 5 | HG00280.hp2 HG02132.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-14968_-49-1495 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0031a0001c0001t0002g0071 | 2 | HG00673.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-49-14970_-49-1495 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
T | TACACACA others(13): Show |
1 | a0001c0001t0001g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-49-14974_-49-1495 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TAC | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0138a0001c0001t0001g0177others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-14956_-49-1495 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TACAC | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG00280.hp1 HG01123.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-14958_-49-1495 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TACACAC | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0108others(44): Show | 49 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-49-14960_-49-1495 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-49-14964_-49-1495 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-49-14966_-49-1495 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750195
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0162a0001c0001t0001g0199 | 2 | HG01261.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-49-14968_-49-1495 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750195 | ||||||
| chr4:46750217
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-14976G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750217 | ||||||
| chr4:46750256
|
T | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-15015A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750256 | ||||||
| chr4:46750267
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-15026C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750267 | ||||||
| chr4:46750337
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-15096G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750337 | ||||||
| chr4:46750438
|
G | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-15197C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750438 | ||||||
| chr4:46750441
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-49-15200G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750441 | ||||||
| chr4:46750524
|
C | CA | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-15284dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750524 | ||||||
| chr4:46750559
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-15318A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750559 | ||||||
| chr4:46750617
|
A | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-15376T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46750617 | ||||||
| chr4:46751050
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-15809G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751050 | ||||||
| chr4:46751135
|
A | AT | 121 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-49-15895dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751135 | ||||||
| chr4:46751152
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-49-15911C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751152 | ||||||
| chr4:46751213
|
C | G | 1 | a0001c0001t0002g0013 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-49-15972G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751213 | ||||||
| chr4:46751349
|
A | AC | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-16109dupG | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751349 | ||||||
| chr4:46751365
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16124T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751365 | ||||||
| chr4:46751388
|
T | C | 1 | a0001c0001t0003g0175 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-49-16147A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751388 | ||||||
| chr4:46751395
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18982.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-49-16154G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751395 | ||||||
| chr4:46751514
|
C | T | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-16273G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751514 | ||||||
| chr4:46751548
|
C | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16307G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751548 | ||||||
| chr4:46751576
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-49-16335T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751576 | ||||||
| chr4:46751594
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-16353A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751594 | ||||||
| chr4:46751649
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-16408T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751649 | ||||||
| chr4:46751656
|
T | TAAAAATG others(170): Show |
1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-16416_-49-1641 others(181): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751656 | ||||||
| chr4:46751688
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16447T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751688 | ||||||
| chr4:46751731
|
G | A | 1 | a0001c0001t0005g0004 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-49-16490C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751731 | ||||||
| chr4:46751821
|
TGTA | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16583_-49-1658 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751821 | ||||||
| chr4:46751826
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-49-16585A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751826 | ||||||
| chr4:46751904
|
C | CT | 56 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(53): Show | 58 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-16664dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751904 | ||||||
| chr4:46751960
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16719T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46751960 | ||||||
| chr4:46752020
|
T | C | 2 | a0001c0001t0002g0065a0001c0001t0002g0073 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-49-16779A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752020 | ||||||
| chr4:46752053
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16812A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752053 | ||||||
| chr4:46752133
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-16892A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752133 | ||||||
| chr4:46752217
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-49-16976A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752217 | ||||||
| chr4:46752272
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17031A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752272 | ||||||
| chr4:46752295
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17054A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752295 | ||||||
| chr4:46752325
|
G | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17084C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752325 | ||||||
| chr4:46752326
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17085C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752326 | ||||||
| chr4:46752369
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-49-17128C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752369 | ||||||
| chr4:46752438
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17197T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752438 | ||||||
| chr4:46752463
|
C | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17222G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752463 | ||||||
| chr4:46752463
|
C | T | 3 | a0001c0001t0002g0065a0001c0001t0002g0073a0001c0001t0006g0106 | 3 | HG02280.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-49-17222G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752463 | ||||||
| chr4:46752561
|
T | G | 2 | a0001c0001t0001g0214a0001c0001t0002g0069 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-49-17320A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752561 | ||||||
| chr4:46752590
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0002g0007 | 2 | HG00642.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-49-17349G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752590 | ||||||
| chr4:46752592
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17351A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752592 | ||||||
| chr4:46752615
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-49-17374C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752615 | ||||||
| chr4:46752660
|
C | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17419G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752660 | ||||||
| chr4:46752686
|
T | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17445A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752686 | ||||||
| chr4:46752720
|
A | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17479T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752720 | ||||||
| chr4:46752779
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-17538C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752779 | ||||||
| chr4:46752785
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17544T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752785 | ||||||
| chr4:46752849
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17608T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752849 | ||||||
| chr4:46752854
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-49-17613G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752854 | ||||||
| chr4:46752925
|
C | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG02970.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-49-17684G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752925 | ||||||
| chr4:46752950
|
G | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17709C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752950 | ||||||
| chr4:46752953
|
CCT | C | 7 | a0001c0001t0003g0176a0001c0001t0003g0235a0001c0001t0003g0245others(4): Show | 7 | HG01346.hp2 HG01934.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-17714_-49-1771 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46752953 | ||||||
| chr4:46753038
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17797T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753038 | ||||||
| chr4:46753042
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-17801C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753042 | ||||||
| chr4:46753052
|
T | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-17811A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753052 | ||||||
| chr4:46753101
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-17860A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753101 | ||||||
| chr4:46753239
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0066 | 2 | HG00423.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-49-17998A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753239 | ||||||
| chr4:46753254
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49-18013C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753254 | ||||||
| chr4:46753287
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18046T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753287 | ||||||
| chr4:46753368
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-18127C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753368 | ||||||
| chr4:46753379
|
A | T | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-18138T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753379 | ||||||
| chr4:46753474
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18233C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753474 | ||||||
| chr4:46753504
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-18263T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753504 | ||||||
| chr4:46753549
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-18308A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753549 | ||||||
| chr4:46753563
|
C | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-18322G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753563 | ||||||
| chr4:46753669
|
T | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18428A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753669 | ||||||
| chr4:46753690
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18449T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753690 | ||||||
| chr4:46753727
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-18486G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753727 | ||||||
| chr4:46753743
|
G | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0087others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-18502C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753743 | ||||||
| chr4:46753797
|
T | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18556A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753797 | ||||||
| chr4:46753837
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-18596T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753837 | ||||||
| chr4:46753870
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18629A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753870 | ||||||
| chr4:46753900
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18659C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753900 | ||||||
| chr4:46753970
|
G | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-18729C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46753970 | ||||||
| chr4:46754014
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-18773G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754014 | ||||||
| chr4:46754086
|
G | C | 48 | a0000c0002t0003g0233a0001c0001t0001g0154a0001c0001t0001g0249others(45): Show | 48 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49-18845C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754086 | ||||||
| chr4:46754108
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-49-18867T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754108 | ||||||
| chr4:46754160
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-49-18919A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754160 | ||||||
| chr4:46754161
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-49-18920A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754161 | ||||||
| chr4:46754193
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-49-18952G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754193 | ||||||
| chr4:46754201
|
T | A | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-18960A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754201 | ||||||
| chr4:46754252
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19011T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754252 | ||||||
| chr4:46754264
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-49-19023C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754264 | ||||||
| chr4:46754323
|
A | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19082T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754323 | ||||||
| chr4:46754528
|
A | G | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-19287T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754528 | ||||||
| chr4:46754540
|
G | C | 1 | a0001c0001t0003g0232 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-49-19299C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754540 | ||||||
| chr4:46754546
|
T | TG | 9 | a0001c0001t0001g0152a0001c0001t0001g0182a0001c0001t0001g0199others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49-19306dupC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754546 | ||||||
| chr4:46754550
|
G | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19309C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754550 | ||||||
| chr4:46754555
|
G | A | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-19314C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754555 | ||||||
| chr4:46754557
|
G | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19316C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754557 | ||||||
| chr4:46754576
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-19335C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754576 | ||||||
| chr4:46754592
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19351T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754592 | ||||||
| chr4:46754617
|
T | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19376A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754617 | ||||||
| chr4:46754623
|
C | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0211 | 2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-49-19382G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754623 | ||||||
| chr4:46754623
|
C | T | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19382G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754623 | ||||||
| chr4:46754634
|
T | A | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-19393A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754634 | ||||||
| chr4:46754652
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-19411T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754652 | ||||||
| chr4:46754714
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49-19473C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754714 | ||||||
| chr4:46754716
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49-19475C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0165 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-49-19476_-49-1947 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-49-19476_-49-1947 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0125 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-49-19476_-49-1947 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-49-19476_-49-1947 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-49-19476_-49-1947 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754716
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0126 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-49-19476_-49-1947 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754716 | ||||||
| chr4:46754718
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0125others(5): Show | 8 | HG01261.hp2 HG02083.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-19477C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0003g0175 | 3 | HG03453.hp1 NA18956.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(3): Show |
8 | a0001c0001t0001g0178a0001c0001t0002g0074a0001c0001t0003g0224others(5): Show | 8 | HG00140.hp2 HG02080.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(5): Show |
17 | a0000c0002t0003g0233a0001c0001t0001g0108a0001c0001t0001g0145others(14): Show | 17 | HG00639.hp2 HG01123.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(7): Show |
34 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0154others(31): Show | 35 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(9): Show |
23 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(20): Show | 24 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0097a0001c0001t0003g0277a0001c0001t0005g0005 | 3 | HG02071.hp1 NA18945.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0155a0001c0001t0003g0201 | 2 | HG01109.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0005g0006 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-49-19478_-49-1947 others(26): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754718
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0157a0001c0001t0003g0264 | 2 | HG00280.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.-49-19478_-49-1947 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754718 | ||||||
| chr4:46754720
|
G | A | 104 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(101): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-49-19479C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754720 | ||||||
| chr4:46754720
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-49-19480_-49-1947 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754720 | ||||||
| chr4:46754720
|
G | GTATATAT others(5): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0163a0001c0001t0001g0221 | 3 | HG01884.hp2 HG02056.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-49-19480_-49-1947 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754720 | ||||||
| chr4:46754720
|
G | GTATATAT others(9): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0220others(1): Show | 4 | HG02451.hp2 NA18941.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-19480_-49-1947 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754720 | ||||||
| chr4:46754720
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-49-19480_-49-1947 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754720 | ||||||
| chr4:46754722
|
G | A | 119 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-49-19481C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754722
|
G | GTA | 3 | a0001c0001t0001g0282a0001c0001t0002g0022a0001c0001t0002g0064 | 3 | HG02818.hp1 HG03209.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-49-19482_-49-1948 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754722
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-49-19482_-49-1948 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754722
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-19482_-49-1948 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754722
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-19482_-49-1948 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754722
|
G | GTATATAT others(33): Show |
1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-19482_-49-1948 others(44): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754722 | ||||||
| chr4:46754724
|
G | A | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-19483C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754724
|
G | GTATA | 48 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0147others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49-19484_-49-1948 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754724
|
G | GTATATA | 3 | a0001c0001t0001g0173a0001c0001t0002g0050a0001c0001t0002g0053 | 3 | HG01433.hp2 NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-49-19484_-49-1948 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754724
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-19484_-49-1948 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754724
|
G | GTATATAT others(13): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG03486.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-49-19484_-49-1948 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754724
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-49-19484_-49-1948 others(26): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754724 | ||||||
| chr4:46754726
|
G | A | 187 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-49-19485C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATA | 3 | a0001c0001t0001g0143a0001c0001t0002g0060a0001c0001t0002g0068 | 3 | HG00609.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-49-19486_-49-1948 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(13): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0191a0001c0001t0002g0047 | 3 | HG03579.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0206 | 2 | HG02148.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(25): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0198 | 2 | NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(36): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(27): Show |
1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-49-19486_-49-1948 others(38): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-49-19486_-49-1948 others(34): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(21): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0203 | 2 | HG00673.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(19): Show |
15 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 15 | HG00621.hp1 HG02615.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49-19486_-49-1948 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754726
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0093 | 2 | HG02818.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-49-19486_-49-1948 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754726 | ||||||
| chr4:46754728
|
G | A | 226 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-49-19487C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-49-19497_-49-1948 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-19505_-49-1948 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(13): Show |
4 | a0001c0001t0001g0205a0001c0001t0001g0280a0001c0001t0001g0287others(1): Show | 4 | HG00544.hp2 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-19507_-49-1948 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(15): Show |
9 | a0001c0001t0001g0086a0001c0001t0001g0113a0001c0001t0001g0134others(6): Show | 9 | HG01257.hp2 HG02109.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(26): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(17): Show |
10 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0202others(7): Show | 11 | HG01516.hp1 HG02083.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(19): Show |
4 | a0001c0001t0001g0119a0001c0001t0002g0049a0001c0001t0002g0054others(1): Show | 4 | HG00423.hp1 HG01243.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0209 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0003g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGATATA others(14): Show |
1 | a0001c0001t0001g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(25): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(5): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0197 | 2 | NA18995.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0161 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(11): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(15): Show |
1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(26): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(17): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0120a0001c0001t0001g0183others(1): Show | 4 | HG03195.hp1 NA18950.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(19): Show |
6 | a0001c0001t0001g0116a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG00735.hp2 HG03017.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTATAT others(21): Show |
2 | a0001c0001t0001g0208a0001c0001t0001g0294 | 2 | HG00642.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTAT others(5): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTAT others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTAT others(17): Show |
5 | a0001c0001t0001g0171a0001c0001t0001g0190a0001c0001t0001g0193others(2): Show | 5 | HG01952.hp1 HG02015.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTAT others(19): Show |
1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTGT others(19): Show |
1 | a0001c0001t0001g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49-19488_-49-1948 others(30): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754728
|
G | GTGTGTGT others(21): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0199 | 2 | HG02071.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-49-19488_-49-1948 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754728 | ||||||
| chr4:46754731
|
T | TATAC | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-19491_-49-1949 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754731 | ||||||
| chr4:46754760
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-19519G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754760 | ||||||
| chr4:46754819
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-19578T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754819 | ||||||
| chr4:46754824
|
A | T | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-19583T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754824 | ||||||
| chr4:46754888
|
A | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-19647T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46754888 | ||||||
| chr4:46755008
|
G | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-19767C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755008 | ||||||
| chr4:46755081
|
G | A | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(134): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-49-19840C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755081 | ||||||
| chr4:46755107
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-19866G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755107 | ||||||
| chr4:46755209
|
A | G | 6 | a0001c0001t0002g0031a0001c0001t0002g0041a0001c0001t0002g0043others(3): Show | 6 | HG00673.hp2 NA18612.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-19968T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755209 | ||||||
| chr4:46755587
|
T | C | 21 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-49-20346A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755587 | ||||||
| chr4:46755713
|
A | C | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-49-20472T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755713 | ||||||
| chr4:46755912
|
A | C | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-20671T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46755912 | ||||||
| chr4:46756081
|
C | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0217 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-49-20840G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756081 | ||||||
| chr4:46756092
|
T | A | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-20851A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756092 | ||||||
| chr4:46756244
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-21003T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756244 | ||||||
| chr4:46756345
|
A | C | 64 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0121others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.-49-21104T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756345 | ||||||
| chr4:46756444
|
C | T | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-21203G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756444 | ||||||
| chr4:46756572
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0195 | 2 | NA18950.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-49-21331T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756572 | ||||||
| chr4:46756771
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-21530T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756771 | ||||||
| chr4:46756922
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-21681T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756922 | ||||||
| chr4:46756925
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0019others(1): Show | 4 | HG00544.hp1 NA18960.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-21684G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756925 | ||||||
| chr4:46756993
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-49-21752A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46756993 | ||||||
| chr4:46757090
|
G | A | 8 | a0001c0001t0003g0175a0001c0001t0003g0224a0001c0001t0003g0228others(5): Show | 8 | HG00140.hp2 HG01952.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-21849C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757090 | ||||||
| chr4:46757297
|
A | G | 130 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-49-22056T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757297 | ||||||
| chr4:46757331
|
T | G | 1 | a0001c0001t0002g0021 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-49-22090A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757331 | ||||||
| chr4:46757379
|
A | G | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-22138T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757379 | ||||||
| chr4:46757469
|
A | AT | 3 | a0001c0001t0001g0002a0001c0001t0001g0215a0001c0001t0001g0295 | 4 | HG01257.hp1 HG01258.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-22229dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757469 | ||||||
| chr4:46757536
|
C | T | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-22295G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757536 | ||||||
| chr4:46757539
|
A | G | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-22298T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757539 | ||||||
| chr4:46757744
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-22503T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46757744 | ||||||
| chr4:46758023
|
T | C | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-49-22782A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758023 | ||||||
| chr4:46758071
|
T | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-22830A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758071 | ||||||
| chr4:46758176
|
TAA | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-22937_-49-2293 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758176 | ||||||
| chr4:46758264
|
TGAGGTAT others(1): Show |
T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-23031_-49-2302 others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758264 | ||||||
| chr4:46758274
|
A | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-23033T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758274 | ||||||
| chr4:46758275
|
G | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-23034C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758275 | ||||||
| chr4:46758322
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-23081A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758322 | ||||||
| chr4:46758353
|
T | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-23112A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758353 | ||||||
| chr4:46758441
|
T | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-23200A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758441 | ||||||
| chr4:46758651
|
A | G | 3 | a0001c0001t0002g0065a0001c0001t0002g0073a0001c0001t0006g0106 | 3 | HG02280.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-49-23410T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46758651 | ||||||
| chr4:46759146
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0280 | 2 | HG00544.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-49-23905C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759146 | ||||||
| chr4:46759168
|
TAAAATCT others(4): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-49-23938_-49-2392 others(15): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759168 | ||||||
| chr4:46759331
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-49-24090A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759331 | ||||||
| chr4:46759380
|
C | T | 1 | a0001c0001t0003g0248 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-49-24139G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759380 | ||||||
| chr4:46759483
|
G | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(53): Show | 58 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-24242C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759483 | ||||||
| chr4:46759573
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(52): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-49-24332G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759573 | ||||||
| chr4:46759604
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-49-24363T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759604 | ||||||
| chr4:46759674
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0053 | 2 | NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-49-24433T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759674 | ||||||
| chr4:46759715
|
T | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0280 | 2 | HG00544.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-49-24474A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759715 | ||||||
| chr4:46759777
|
T | A | 1 | a0001c0001t0002g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-49-24536A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759777 | ||||||
| chr4:46759777
|
T | TTATCTTA others(18): Show |
3 | a0001c0001t0002g0019a0001c0001t0006g0106a0001c0001t0006g0172 | 3 | HG00544.hp1 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-49-24561_-49-2453 others(29): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759777 | ||||||
| chr4:46759777
|
TTATCTTA others(18): Show |
T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0191others(1): Show | 4 | HG01257.hp2 HG02145.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-24561_-49-2453 others(29): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759777 | ||||||
| chr4:46759777
|
TTATCTTA others(43): Show |
T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-24586_-49-2453 others(54): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759777 | ||||||
| chr4:46759785
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18982.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-49-24544A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759785 | ||||||
| chr4:46759804
|
A | ATCT | 3 | a0001c0001t0001g0178a0001c0001t0001g0282a0001c0001t0003g0107 | 3 | HG02922.hp2 HG03209.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-49-24566_-49-2456 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759804 | ||||||
| chr4:46759807
|
TTATATAA others(15): Show |
T | 119 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-49-24588_-49-2456 others(26): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759807 | ||||||
| chr4:46759821
|
TAAGTCAT others(20): Show |
T | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-24607_-49-2458 others(31): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759821 | ||||||
| chr4:46759844
|
T | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-24603A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759844 | ||||||
| chr4:46759874
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-24633C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759874 | ||||||
| chr4:46759877
|
A | T | 4 | a0001c0001t0001g0178a0001c0001t0002g0001a0001c0001t0002g0051others(1): Show | 5 | HG02922.hp2 NA18955.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-24636T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759877 | ||||||
| chr4:46759899
|
GTCTTA | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0121others(1): Show | 4 | HG03486.hp2 HG03490.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-24663_-49-2465 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759899 | ||||||
| chr4:46759900
|
T | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-24659A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759900 | ||||||
| chr4:46759943
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-24702T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759943 | ||||||
| chr4:46759968
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-24727G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46759968 | ||||||
| chr4:46760128
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-24887G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760128 | ||||||
| chr4:46760251
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-25010A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760251 | ||||||
| chr4:46760366
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-25125T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760366 | ||||||
| chr4:46760465
|
C | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-25224G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760465 | ||||||
| chr4:46760521
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-49-25280G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760521 | ||||||
| chr4:46760591
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-49-25350C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46760591 | ||||||
| chr4:46761063
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49-25822C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761063 | ||||||
| chr4:46761082
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-25841T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761082 | ||||||
| chr4:46761279
|
A | G | 10 | a0000c0002t0003g0233a0001c0001t0003g0185a0001c0001t0003g0231others(7): Show | 10 | HG02132.hp2 NA18612.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-26038T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761279 | ||||||
| chr4:46761320
|
G | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-26079C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761320 | ||||||
| chr4:46761671
|
G | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-26430C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761671 | ||||||
| chr4:46761723
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-26482T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761723 | ||||||
| chr4:46761733
|
A | G | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-49-26492T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761733 | ||||||
| chr4:46761828
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(50): Show | 55 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-49-26587C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761828 | ||||||
| chr4:46761886
|
A | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-26645T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761886 | ||||||
| chr4:46761887
|
A | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-26646T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761887 | ||||||
| chr4:46761908
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-26667G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761908 | ||||||
| chr4:46761924
|
CT | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-26684delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761924 | ||||||
| chr4:46761935
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-49-26694A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761935 | ||||||
| chr4:46761963
|
A | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-26722T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46761963 | ||||||
| chr4:46762098
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-49-26857A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762098 | ||||||
| chr4:46762211
|
T | TTAATATG others(60): Show |
114 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(111): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-49-26971_-49-2697 others(71): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762211 | ||||||
| chr4:46762225
|
A | ATTTATAT others(60): Show |
1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-26985_-49-2698 others(71): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762225 | ||||||
| chr4:46762261
|
A | ATATATTT others(58): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG02970.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-49-27021_-49-2702 others(69): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762261 | ||||||
| chr4:46762284
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49-27043A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762284 | ||||||
| chr4:46762348
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-49-27107A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762348 | ||||||
| chr4:46762354
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0294 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-49-27113G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762354 | ||||||
| chr4:46762371
|
CACAAT | C | 21 | a0001c0001t0001g0117a0001c0001t0001g0161a0001c0001t0001g0171others(18): Show | 21 | HG01433.hp1 HG01952.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-49-27135_-49-2713 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762371 | ||||||
| chr4:46762408
|
T | C | 1 | a0001c0001t0003g0235 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-49-27167A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762408 | ||||||
| chr4:46762452
|
C | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(53): Show | 58 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-27211G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762452 | ||||||
| chr4:46762461
|
G | GTATATAT others(2): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-27221_-49-2722 others(13): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762461 | ||||||
| chr4:46762467
|
G | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-27226C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762467 | ||||||
| chr4:46762694
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | NA18941.hp2 NA18957.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-27453G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762694 | ||||||
| chr4:46762739
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-27498T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762739 | ||||||
| chr4:46762790
|
A | T | 3 | a0001c0001t0003g0255a0001c0001t0003g0263a0001c0001t0003g0274 | 3 | HG01070.hp2 HG01934.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-49-27549T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762790 | ||||||
| chr4:46762807
|
A | C | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49-27566T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762807 | ||||||
| chr4:46762812
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27571A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762812 | ||||||
| chr4:46762903
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27662A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762903 | ||||||
| chr4:46762928
|
C | CATATATA others(30): Show |
2 | a0001c0001t0001g0237a0001c0001t0002g0047 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49-27724_-49-2768 others(41): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762928 | ||||||
| chr4:46762928
|
C | CATATATA others(67): Show |
1 | a0001c0001t0001g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-49-27688_-49-2768 others(78): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762928 | ||||||
| chr4:46762973
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27732A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762973 | ||||||
| chr4:46762974
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27733T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762974 | ||||||
| chr4:46762978
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27737G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762978 | ||||||
| chr4:46762981
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-27740T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46762981 | ||||||
| chr4:46763005
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49-27764T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763005 | ||||||
| chr4:46763011
|
TTATAATA | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0289a0001c0001t0001g0293 | 3 | NA18950.hp2 NA18952.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-49-27777_-49-2777 others(11): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763011 | ||||||
| chr4:46763017
|
T | TATATAAT others(43): Show |
1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-27777_-49-2777 others(54): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763017 | ||||||
| chr4:46763050
|
T | TAATATGT others(16): Show |
3 | a0001c0001t0001g0282a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-49-27832_-49-2781 others(27): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763050 | ||||||
| chr4:46763052
|
A | T | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-27811T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763052 | ||||||
| chr4:46763056
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-27815C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763056 | ||||||
| chr4:46763059
|
A | T | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-27818T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763059 | ||||||
| chr4:46763084
|
ATAT | A | 30 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0283others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-49-27846_-49-2784 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763084 | ||||||
| chr4:46763118
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-27877T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763118 | ||||||
| chr4:46763142
|
T | TATATA | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-27906_-49-2790 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763142 | ||||||
| chr4:46763164
|
C | A | 1 | a0001c0001t0003g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-49-27923G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763164 | ||||||
| chr4:46763181
|
C | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-27940G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763181 | ||||||
| chr4:46763183
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27942C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763183 | ||||||
| chr4:46763200
|
GATATTAT others(21): Show |
G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-27987_-49-2796 others(32): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763200 | ||||||
| chr4:46763220
|
T | G | 1 | a0001c0001t0003g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-49-27979A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763220 | ||||||
| chr4:46763224
|
C | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-27983G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763224 | ||||||
| chr4:46763234
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-27993T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763234 | ||||||
| chr4:46763272
|
G | A | 62 | a0001c0001t0001g0092a0001c0001t0001g0121a0001c0001t0001g0123others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-49-28031C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763272 | ||||||
| chr4:46763278
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-49-28037T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763278 | ||||||
| chr4:46763297
|
A | G | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-28056T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763297 | ||||||
| chr4:46763325
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-49-28084G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763325 | ||||||
| chr4:46763522
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-28281C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763522 | ||||||
| chr4:46763577
|
T | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-28336A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763577 | ||||||
| chr4:46763595
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49-28354T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763595 | ||||||
| chr4:46763741
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-49-28500A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763741 | ||||||
| chr4:46763759
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-28518T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763759 | ||||||
| chr4:46763967
|
C | T | 128 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-49-28726G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46763967 | ||||||
| chr4:46764156
|
A | G | 62 | a0000c0002t0003g0233a0001c0001t0001g0249a0001c0001t0001g0250others(59): Show | 62 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-49-28915T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764156 | ||||||
| chr4:46764280
|
C | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG02970.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-49-29039G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764280 | ||||||
| chr4:46764282
|
C | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-29041G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764282 | ||||||
| chr4:46764329
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02083.hp2 NA18965.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-29088C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764329 | ||||||
| chr4:46764374
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0065 | 3 | HG02145.hp2 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-29133C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764374 | ||||||
| chr4:46764388
|
T | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0223 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-49-29147A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764388 | ||||||
| chr4:46764474
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-29233G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764474 | ||||||
| chr4:46764674
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-29433G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764674 | ||||||
| chr4:46764679
|
CA | C | 241 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-49-29439delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764679 | ||||||
| chr4:46764749
|
G | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-29508C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764749 | ||||||
| chr4:46764888
|
A | G | 19 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0123others(16): Show | 19 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-29647T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46764888 | ||||||
| chr4:46765202
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-29961G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765202 | ||||||
| chr4:46765324
|
C | CG | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-30084dupC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765324 | ||||||
| chr4:46765396
|
T | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-30155A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765396 | ||||||
| chr4:46765417
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-49-30176G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765417 | ||||||
| chr4:46765464
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49-30223C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765464 | ||||||
| chr4:46765529
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0200 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-49-30288A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765529 | ||||||
| chr4:46765602
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | NA18941.hp2 NA18957.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-49-30361G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765602 | ||||||
| chr4:46765684
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-49-30443G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765684 | ||||||
| chr4:46765951
|
AG | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-30711delC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765951 | ||||||
| chr4:46765962
|
C | A | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-49-30721G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46765962 | ||||||
| chr4:46766109
|
A | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-30868T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766109 | ||||||
| chr4:46766116
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-30875G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766116 | ||||||
| chr4:46766136
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-30895T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766136 | ||||||
| chr4:46766422
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0280 | 2 | HG00544.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-49-31181C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766422 | ||||||
| chr4:46766517
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-31276A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766517 | ||||||
| chr4:46766587
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-49-31346C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766587 | ||||||
| chr4:46766636
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-31395C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766636 | ||||||
| chr4:46766695
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-49-31454G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766695 | ||||||
| chr4:46766706
|
G | GA | 116 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0089others(113): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.-49-31466dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766706 | ||||||
| chr4:46766707
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0002g0047 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49-31466T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46766707 | ||||||
| chr4:46767095
|
A | C | 64 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0121others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.-49-31854T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767095 | ||||||
| chr4:46767192
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-31951T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767192 | ||||||
| chr4:46767209
|
A | C | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-31968T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767209 | ||||||
| chr4:46767354
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-32113C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767354 | ||||||
| chr4:46767423
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-49-32182G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767423 | ||||||
| chr4:46767636
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-32395T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767636 | ||||||
| chr4:46767712
|
C | T | 1 | a0001c0001t0003g0003 | 2 | NA18957.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-49-32471G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767712 | ||||||
| chr4:46767720
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-32479A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767720 | ||||||
| chr4:46767859
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-32618A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46767859 | ||||||
| chr4:46768049
|
A | G | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-49-32808T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768049 | ||||||
| chr4:46768073
|
A | G | 127 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-49-32832T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768073 | ||||||
| chr4:46768104
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0004g0048 | 2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-49-32863C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768104 | ||||||
| chr4:46768236
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-32995G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768236 | ||||||
| chr4:46768353
|
ATCTAGCT others(6): Show |
A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-33125_-49-3311 others(17): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768353 | ||||||
| chr4:46768394
|
T | G | 1 | a0001c0001t0002g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-49-33153A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768394 | ||||||
| chr4:46768410
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-33169C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768410 | ||||||
| chr4:46768495
|
G | C | 3 | a0001c0001t0001g0105a0001c0001t0003g0084a0001c0001t0003g0085 | 3 | NA18939.hp2 NA19000.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-49-33254C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768495 | ||||||
| chr4:46768740
|
G | A | 4 | a0001c0001t0003g0234a0001c0001t0003g0252a0001c0001t0003g0267others(1): Show | 4 | HG02071.hp1 HG02165.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-33499C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768740 | ||||||
| chr4:46768997
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-49-33756G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46768997 | ||||||
| chr4:46769029
|
A | G | 62 | a0000c0002t0003g0233a0001c0001t0001g0249a0001c0001t0001g0250others(59): Show | 62 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-49-33788T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769029 | ||||||
| chr4:46769230
|
A | G | 47 | a0000c0002t0003g0233a0001c0001t0001g0249a0001c0001t0001g0250others(44): Show | 47 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-49-33989T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769230 | ||||||
| chr4:46769288
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-34047T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769288 | ||||||
| chr4:46769342
|
G | A | 142 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(139): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-49-34101C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769342 | ||||||
| chr4:46769442
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-34201C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769442 | ||||||
| chr4:46769459
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-34218G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769459 | ||||||
| chr4:46769581
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-34340C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769581 | ||||||
| chr4:46769669
|
T | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0015a0001c0001t0002g0019others(1): Show | 4 | HG00544.hp1 NA18960.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-34428A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769669 | ||||||
| chr4:46769844
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0198 | 3 | NA18974.hp2 NA18994.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-49-34603G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769844 | ||||||
| chr4:46769863
|
T | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-34622A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769863 | ||||||
| chr4:46769868
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-34627A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46769868 | ||||||
| chr4:46770206
|
C | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-49-34965G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770206 | ||||||
| chr4:46770270
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-49-35029A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770270 | ||||||
| chr4:46770314
|
A | G | 62 | a0000c0002t0003g0233a0001c0001t0001g0249a0001c0001t0001g0250others(59): Show | 62 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-49-35073T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770314 | ||||||
| chr4:46770413
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-35172G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770413 | ||||||
| chr4:46770455
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49-35214A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770455 | ||||||
| chr4:46770645
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(53): Show | 58 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-35404G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770645 | ||||||
| chr4:46770661
|
G | GA | 65 | a0000c0002t0003g0233a0001c0001t0001g0109a0001c0001t0001g0110others(62): Show | 65 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-49-35421dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770661 | ||||||
| chr4:46770661
|
G | GAA | 56 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(53): Show | 58 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-35422_-49-3542 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770661 | ||||||
| chr4:46770877
|
G | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-35636C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46770877 | ||||||
| chr4:46771096
|
G | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0203a0001c0001t0001g0213 | 3 | HG00673.hp1 NA19003.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-49-35855C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771096 | ||||||
| chr4:46771213
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-49-35972A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771213 | ||||||
| chr4:46771261
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-36020C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771261 | ||||||
| chr4:46771438
|
C | T | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-36197G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771438 | ||||||
| chr4:46771462
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0002g0040 | 2 | HG02132.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-49-36221C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771462 | ||||||
| chr4:46771488
|
G | A | 123 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-36247C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771488 | ||||||
| chr4:46771526
|
C | T | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-36285G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771526 | ||||||
| chr4:46771581
|
G | C | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-36340C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771581 | ||||||
| chr4:46771679
|
G | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0002g0023others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-36438C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771679 | ||||||
| chr4:46771764
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-49-36523G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771764 | ||||||
| chr4:46771987
|
T | G | 1 | a0001c0001t0002g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-49-36746A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46771987 | ||||||
| chr4:46772168
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-36927A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772168 | ||||||
| chr4:46772204
|
A | G | 1 | a0001c0001t0003g0100 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-49-36963T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772204 | ||||||
| chr4:46772398
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-37157A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772398 | ||||||
| chr4:46772452
|
A | G | 118 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(115): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-49-37211T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772452 | ||||||
| chr4:46772696
|
C | T | 5 | a0001c0001t0003g0176a0001c0001t0003g0245a0001c0001t0003g0269others(2): Show | 5 | HG01346.hp2 HG01934.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-37455G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772696 | ||||||
| chr4:46772707
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-37466A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772707 | ||||||
| chr4:46772887
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-49-37646A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772887 | ||||||
| chr4:46772920
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-49-37679T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772920 | ||||||
| chr4:46772962
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-49-37721A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46772962 | ||||||
| chr4:46773121
|
T | C | 5 | a0001c0001t0001g0091a0001c0001t0001g0158a0001c0001t0001g0216others(2): Show | 5 | HG01256.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-37880A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773121 | ||||||
| chr4:46773209
|
T | C | 124 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(121): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-49-37968A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773209 | ||||||
| chr4:46773254
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49-38013C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773254 | ||||||
| chr4:46773258
|
A | G | 122 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-49-38017T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773258 | ||||||
| chr4:46773369
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-38128T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773369 | ||||||
| chr4:46773406
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(51): Show | 56 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-49-38165C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773406 | ||||||
| chr4:46773470
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-49-38229C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773470 | ||||||
| chr4:46773576
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-49-38335T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773576 | ||||||
| chr4:46773580
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-38339T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773580 | ||||||
| chr4:46773606
|
A | G | 8 | a0001c0001t0003g0175a0001c0001t0003g0224a0001c0001t0003g0228others(5): Show | 8 | HG00140.hp2 HG01952.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-38365T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773606 | ||||||
| chr4:46773666
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-49-38425G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773666 | ||||||
| chr4:46773704
|
G | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0191 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-49-38463C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773704 | ||||||
| chr4:46773712
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-49-38471A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773712 | ||||||
| chr4:46773822
|
TTAGTC | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-38586_-49-3858 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773822 | ||||||
| chr4:46773953
|
C | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0101others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-38712G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773953 | ||||||
| chr4:46773985
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-49-38744C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46773985 | ||||||
| chr4:46774047
|
C | T | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-49-38806G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774047 | ||||||
| chr4:46774178
|
GCCC | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-38940_-49-3893 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774178 | ||||||
| chr4:46774200
|
A | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-38959T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774200 | ||||||
| chr4:46774221
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-38980G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774221 | ||||||
| chr4:46774332
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-39091A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774332 | ||||||
| chr4:46774349
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-39108A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774349 | ||||||
| chr4:46774358
|
G | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-39117C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774358 | ||||||
| chr4:46774383
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-49-39142A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774383 | ||||||
| chr4:46774497
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-39256G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774497 | ||||||
| chr4:46774556
|
G | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-39315C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774556 | ||||||
| chr4:46774866
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49-39625C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46774866 | ||||||
| chr4:46775076
|
T | A | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-39835A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775076 | ||||||
| chr4:46775081
|
CA | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-39841delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775081 | ||||||
| chr4:46775105
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-49-39864G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775105 | ||||||
| chr4:46775136
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-39895A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775136 | ||||||
| chr4:46775186
|
G | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-39945C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775186 | ||||||
| chr4:46775227
|
A | G | 14 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0120others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-49-39986T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775227 | ||||||
| chr4:46775274
|
G | A | 1 | a0001c0001t0004g0027 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-49-40033C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775274 | ||||||
| chr4:46775321
|
T | C | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-49-40080A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775321 | ||||||
| chr4:46775566
|
C | T | 5 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-40325G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775566 | ||||||
| chr4:46775975
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02083.hp2 NA18965.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-40734T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46775975 | ||||||
| chr4:46776101
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-49-40860G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776101 | ||||||
| chr4:46776286
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49-41045A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776286 | ||||||
| chr4:46776358
|
T | TCACTACA others(293): Show |
1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-49-41118_-49-4111 others(304): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776358 | ||||||
| chr4:46776393
|
A | AGT | 15 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0095others(12): Show | 15 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-41154_-49-4115 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776393 | ||||||
| chr4:46776393
|
AGT | A | 121 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-49-41154_-49-4115 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776393 | ||||||
| chr4:46776393
|
AGTGT | A | 3 | a0001c0001t0001g0097a0001c0001t0002g0038a0001c0001t0002g0060 | 3 | HG00609.hp1 HG02004.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-49-41156_-49-4115 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776393 | ||||||
| chr4:46776460
|
G | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-41219C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776460 | ||||||
| chr4:46776506
|
C | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-41265G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776506 | ||||||
| chr4:46776835
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-49-41594T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776835 | ||||||
| chr4:46776915
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-41674A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46776915 | ||||||
| chr4:46777016
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-41775G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777016 | ||||||
| chr4:46777033
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-49-41792A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777033 | ||||||
| chr4:46777112
|
T | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-41871A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777112 | ||||||
| chr4:46777231
|
A | C | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49-41990T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777231 | ||||||
| chr4:46777389
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-49-42148T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777389 | ||||||
| chr4:46777442
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49-42201A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777442 | ||||||
| chr4:46777443
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-42202C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777443 | ||||||
| chr4:46777585
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0128 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-49-42344C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777585 | ||||||
| chr4:46777767
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-42526A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46777767 | ||||||
| chr4:46778747
|
G | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-49-43506C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46778747 | ||||||
| chr4:46778767
|
C | A | 1 | a0001c0001t0003g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-49-43526G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46778767 | ||||||
| chr4:46778965
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49-43724A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46778965 | ||||||
| chr4:46778987
|
T | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-43746A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46778987 | ||||||
| chr4:46779090
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-43849C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779090 | ||||||
| chr4:46779111
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-49-43870A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779111 | ||||||
| chr4:46779197
|
C | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18966.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-49-43956G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779197 | ||||||
| chr4:46779248
|
T | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-44007A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779248 | ||||||
| chr4:46779336
|
T | C | 5 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-44095A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779336 | ||||||
| chr4:46779455
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-49-44214T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779455 | ||||||
| chr4:46779631
|
T | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-44390A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779631 | ||||||
| chr4:46779635
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-44394A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779635 | ||||||
| chr4:46779657
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-44416T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779657 | ||||||
| chr4:46779688
|
C | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-44447G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779688 | ||||||
| chr4:46779694
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-44453G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779694 | ||||||
| chr4:46779850
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-44609C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46779850 | ||||||
| chr4:46780172
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-44931A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780172 | ||||||
| chr4:46780202
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-44961C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780202 | ||||||
| chr4:46780222
|
C | T | 1 | a0001c0001t0007g0239 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-49-44981G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780222 | ||||||
| chr4:46780237
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-44996G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780237 | ||||||
| chr4:46780244
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45003G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780244 | ||||||
| chr4:46780245
|
G | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(1): Show | 4 | HG02109.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-45004C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780245 | ||||||
| chr4:46780267
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45026G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780267 | ||||||
| chr4:46780313
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-45072G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780313 | ||||||
| chr4:46780345
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45104C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780345 | ||||||
| chr4:46780370
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-45129T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780370 | ||||||
| chr4:46780396
|
T | A | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-49-45155A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780396 | ||||||
| chr4:46780445
|
A | T | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-45204T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780445 | ||||||
| chr4:46780449
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45208T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780449 | ||||||
| chr4:46780483
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-49-45242G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780483 | ||||||
| chr4:46780511
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45270G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780511 | ||||||
| chr4:46780548
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45307C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780548 | ||||||
| chr4:46780693
|
CT | C | 3 | a0001c0001t0003g0230a0001c0001t0004g0008a0001c0001t0004g0035 | 3 | HG00140.hp2 HG01952.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-49-45453delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780693 | ||||||
| chr4:46780755
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45514A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780755 | ||||||
| chr4:46780838
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45597G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780838 | ||||||
| chr4:46780839
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45598T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780839 | ||||||
| chr4:46780917
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-45676A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780917 | ||||||
| chr4:46780924
|
C | A | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-49-45683G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780924 | ||||||
| chr4:46780936
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49-45695G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46780936 | ||||||
| chr4:46781129
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-45888T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781129 | ||||||
| chr4:46781177
|
A | C | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-45936T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781177 | ||||||
| chr4:46781361
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46120T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781361 | ||||||
| chr4:46781694
|
G | C | 2 | a0001c0001t0001g0237a0001c0001t0002g0047 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49-46453C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781694 | ||||||
| chr4:46781708
|
G | A | 5 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-46467C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781708 | ||||||
| chr4:46781711
|
T | C | 130 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-49-46470A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781711 | ||||||
| chr4:46781743
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46502C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781743 | ||||||
| chr4:46781746
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46505C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781746 | ||||||
| chr4:46781764
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46523T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781764 | ||||||
| chr4:46781792
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-49-46551C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781792 | ||||||
| chr4:46781835
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46594T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781835 | ||||||
| chr4:46781841
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46600A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781841 | ||||||
| chr4:46781845
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46604G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781845 | ||||||
| chr4:46781885
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-49-46644C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781885 | ||||||
| chr4:46781893
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-46652C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781893 | ||||||
| chr4:46781926
|
G | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0198 | 3 | NA18974.hp2 NA18994.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-49-46685C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781926 | ||||||
| chr4:46781930
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46689T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781930 | ||||||
| chr4:46781986
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG03579.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49-46745G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46781986 | ||||||
| chr4:46782042
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-46801G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782042 | ||||||
| chr4:46782049
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-46808C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782049 | ||||||
| chr4:46782054
|
G | A | 1 | a0001c0001t0003g0003 | 2 | NA18957.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-49-46813C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782054 | ||||||
| chr4:46782056
|
G | A | 2 | a0001c0001t0003g0261a0001c0001t0003g0266 | 2 | NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-49-46815C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782056 | ||||||
| chr4:46782178
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-46937A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782178 | ||||||
| chr4:46782310
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-49-47069G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782310 | ||||||
| chr4:46782360
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47119G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782360 | ||||||
| chr4:46782362
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47121C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782362 | ||||||
| chr4:46782363
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-49-47122A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782363 | ||||||
| chr4:46782420
|
A | ATTGTAAA others(34): Show |
202 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-49-47220_-49-4718 others(45): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782420 | ||||||
| chr4:46782520
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49-47279C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782520 | ||||||
| chr4:46782522
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-49-47281C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782522 | ||||||
| chr4:46782530
|
TA | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG03579.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49-47290delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782530 | ||||||
| chr4:46782534
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47293T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782534 | ||||||
| chr4:46782620
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47379T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782620 | ||||||
| chr4:46782657
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47416C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782657 | ||||||
| chr4:46782662
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47421A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782662 | ||||||
| chr4:46782676
|
A | G | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-47435T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782676 | ||||||
| chr4:46782718
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-49-47477T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782718 | ||||||
| chr4:46782726
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47485C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782726 | ||||||
| chr4:46782757
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47516A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782757 | ||||||
| chr4:46782789
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-49-47548G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782789 | ||||||
| chr4:46782804
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47563A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782804 | ||||||
| chr4:46782901
|
T | TAAGAACT others(311): Show |
1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-47661_-49-4766 others(322): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782901 | ||||||
| chr4:46782933
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-47692C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782933 | ||||||
| chr4:46782936
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0190 | 2 | HG02015.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-49-47695A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46782936 | ||||||
| chr4:46783016
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-49-47775T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783016 | ||||||
| chr4:46783094
|
G | T | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-47853C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783094 | ||||||
| chr4:46783132
|
A | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-47891T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783132 | ||||||
| chr4:46783226
|
A | G | 1 | a0001c0001t0003g0261 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-49-47985T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783226 | ||||||
| chr4:46783314
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-48073T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783314 | ||||||
| chr4:46783526
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0254 | 3 | HG02056.hp2 NA18954.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-49-48285T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783526 | ||||||
| chr4:46783635
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-48394G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783635 | ||||||
| chr4:46783648
|
A | C | 1 | a0001c0001t0002g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-49-48407T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783648 | ||||||
| chr4:46783669
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-48428T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783669 | ||||||
| chr4:46783734
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-48493T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783734 | ||||||
| chr4:46783915
|
T | C | 1 | a0001c0001t0003g0279 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-49-48674A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783915 | ||||||
| chr4:46783924
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-49-48683G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46783924 | ||||||
| chr4:46784209
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-49-48968T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784209 | ||||||
| chr4:46784348
|
C | T | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-49-49107G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784348 | ||||||
| chr4:46784355
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49114C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784355 | ||||||
| chr4:46784355
|
G | T | 1 | a0001c0001t0003g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-49114C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784355 | ||||||
| chr4:46784373
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-49-49132A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784373 | ||||||
| chr4:46784379
|
C | A | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-49138G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784379 | ||||||
| chr4:46784437
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-49196G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784437 | ||||||
| chr4:46784450
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49209A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784450 | ||||||
| chr4:46784484
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49243T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784484 | ||||||
| chr4:46784494
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-49253C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784494 | ||||||
| chr4:46784521
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49280T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784521 | ||||||
| chr4:46784556
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49315G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784556 | ||||||
| chr4:46784582
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49341T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784582 | ||||||
| chr4:46784758
|
A | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-49517T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784758 | ||||||
| chr4:46784811
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-49570T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784811 | ||||||
| chr4:46784826
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49585T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784826 | ||||||
| chr4:46784990
|
T | C | 9 | a0001c0001t0003g0144a0001c0001t0003g0201a0001c0001t0003g0225others(6): Show | 9 | HG01109.hp2 HG01261.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-49749A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46784990 | ||||||
| chr4:46785047
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49806T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785047 | ||||||
| chr4:46785136
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-49895A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785136 | ||||||
| chr4:46785178
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49937C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785178 | ||||||
| chr4:46785193
|
A | C | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-49952T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785193 | ||||||
| chr4:46785204
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-49963A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785204 | ||||||
| chr4:46785249
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-50008A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785249 | ||||||
| chr4:46785333
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50092T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785333 | ||||||
| chr4:46785375
|
A | AT | 6 | a0001c0001t0001g0082a0001c0001t0001g0101a0001c0001t0001g0124others(3): Show | 6 | HG00621.hp2 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-50135dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785375 | ||||||
| chr4:46785375
|
AT | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-50135delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785375 | ||||||
| chr4:46785388
|
T | G | 1 | a0001c0001t0003g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-49-50147A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785388 | ||||||
| chr4:46785413
|
A | G | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-49-50172T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785413 | ||||||
| chr4:46785419
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50178T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785419 | ||||||
| chr4:46785518
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50277T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785518 | ||||||
| chr4:46785529
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-49-50288G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785529 | ||||||
| chr4:46785530
|
A | G | 202 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-49-50289T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785530 | ||||||
| chr4:46785600
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49-50359A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785600 | ||||||
| chr4:46785628
|
C | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-50387G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785628 | ||||||
| chr4:46785643
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-50402A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785643 | ||||||
| chr4:46785692
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0191 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-49-50451T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785692 | ||||||
| chr4:46785722
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50481C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785722 | ||||||
| chr4:46785883
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-49-50642C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785883 | ||||||
| chr4:46785985
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50744A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785985 | ||||||
| chr4:46785995
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-49-50754A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46785995 | ||||||
| chr4:46786012
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50771C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786012 | ||||||
| chr4:46786019
|
C | A | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-49-50778G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786019 | ||||||
| chr4:46786043
|
C | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-50802G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786043 | ||||||
| chr4:46786074
|
A | T | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-50833T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786074 | ||||||
| chr4:46786091
|
TA | T | 14 | a0001c0001t0001g0094a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01106.hp2 HG01167.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-49-50851delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786091 | ||||||
| chr4:46786237
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-50996T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786237 | ||||||
| chr4:46786334
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-51093A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786334 | ||||||
| chr4:46786579
|
T | A | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-51338A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786579 | ||||||
| chr4:46786594
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-51353G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786594 | ||||||
| chr4:46786665
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-51424G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786665 | ||||||
| chr4:46786682
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-49-51441A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786682 | ||||||
| chr4:46786773
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-49-51532A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786773 | ||||||
| chr4:46786923
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-49-51682C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786923 | ||||||
| chr4:46786934
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-49-51693C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786934 | ||||||
| chr4:46786989
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-51748A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46786989 | ||||||
| chr4:46787112
|
A | C | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-51871T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787112 | ||||||
| chr4:46787214
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-49-51973C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787214 | ||||||
| chr4:46787277
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49-52036C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787277 | ||||||
| chr4:46787360
|
A | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-52119T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787360 | ||||||
| chr4:46787403
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52162A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787403 | ||||||
| chr4:46787452
|
A | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-52211T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787452 | ||||||
| chr4:46787461
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52220A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787461 | ||||||
| chr4:46787478
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52237A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787478 | ||||||
| chr4:46787520
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52279G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787520 | ||||||
| chr4:46787549
|
G | T | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-52308C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787549 | ||||||
| chr4:46787670
|
G | T | 1 | a0001c0001t0003g0279 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-49-52429C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787670 | ||||||
| chr4:46787791
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-52550G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787791 | ||||||
| chr4:46787881
|
T | C | 132 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-49-52640A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787881 | ||||||
| chr4:46787939
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52698A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787939 | ||||||
| chr4:46787940
|
A | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-52699T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787940 | ||||||
| chr4:46787968
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52727C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787968 | ||||||
| chr4:46787969
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-52728G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787969 | ||||||
| chr4:46787985
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52744G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46787985 | ||||||
| chr4:46788030
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52789C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788030 | ||||||
| chr4:46788047
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52806A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788047 | ||||||
| chr4:46788123
|
CGTAGTAG others(4): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-52893_-49-5288 others(15): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788123 | ||||||
| chr4:46788137
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49-52896T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788137 | ||||||
| chr4:46788324
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-49-53083A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788324 | ||||||
| chr4:46788349
|
T | C | 4 | a0001c0001t0001g0099a0001c0001t0002g0001a0001c0001t0002g0051others(1): Show | 5 | NA18955.hp1 NA19011.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-53108A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788349 | ||||||
| chr4:46788430
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-49-53189A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788430 | ||||||
| chr4:46788438
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49-53197G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788438 | ||||||
| chr4:46788493
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53252C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788493 | ||||||
| chr4:46788526
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-53285T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788526 | ||||||
| chr4:46788651
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-49-53410A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788651 | ||||||
| chr4:46788672
|
T | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-53431A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788672 | ||||||
| chr4:46788688
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53447A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788688 | ||||||
| chr4:46788831
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53590G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788831 | ||||||
| chr4:46788851
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-49-53610A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788851 | ||||||
| chr4:46788866
|
A | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-53625T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788866 | ||||||
| chr4:46788923
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53682C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46788923 | ||||||
| chr4:46789000
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53759C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789000 | ||||||
| chr4:46789107
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53866G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789107 | ||||||
| chr4:46789155
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-53914A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789155 | ||||||
| chr4:46789251
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49-54010T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789251 | ||||||
| chr4:46789327
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-54086A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789327 | ||||||
| chr4:46789337
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0183 | 2 | NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-49-54096G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789337 | ||||||
| chr4:46789659
|
C | T | 7 | a0001c0001t0001g0220a0001c0001t0001g0282a0001c0001t0002g0073others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-54418G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789659 | ||||||
| chr4:46789730
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-54489G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789730 | ||||||
| chr4:46789760
|
CTG | C | 9 | a0001c0001t0003g0144a0001c0001t0003g0201a0001c0001t0003g0225others(6): Show | 9 | HG01109.hp2 HG01261.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-54521_-49-5452 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46789760 | ||||||
| chr4:46790004
|
TA | T | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-54764delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790004 | ||||||
| chr4:46790160
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+54800G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790160 | ||||||
| chr4:46790177
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-50+54783G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790177 | ||||||
| chr4:46790213
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+54747A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790213 | ||||||
| chr4:46790269
|
A | T | 1 | a0001c0001t0007g0239 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-50+54691T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790269 | ||||||
| chr4:46790296
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+54664C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790296 | ||||||
| chr4:46790307
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-50+54653G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790307 | ||||||
| chr4:46790423
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+54537T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790423 | ||||||
| chr4:46790456
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+54504A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790456 | ||||||
| chr4:46790473
|
TTTATTAC | T | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+54480_-50+5448 others(11): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790473 | ||||||
| chr4:46790661
|
C | T | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+54299G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790661 | ||||||
| chr4:46790688
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+54272G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790688 | ||||||
| chr4:46790721
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+54239G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790721 | ||||||
| chr4:46790729
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+54231G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790729 | ||||||
| chr4:46790905
|
T | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-50+54055A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790905 | ||||||
| chr4:46790962
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53998G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46790962 | ||||||
| chr4:46791024
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53936G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791024 | ||||||
| chr4:46791051
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53909C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791051 | ||||||
| chr4:46791085
|
C | T | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+53875G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791085 | ||||||
| chr4:46791091
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53869A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791091 | ||||||
| chr4:46791199
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53761C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791199 | ||||||
| chr4:46791222
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-50+53738C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791222 | ||||||
| chr4:46791251
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53709G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791251 | ||||||
| chr4:46791300
|
T | C | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-50+53660A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791300 | ||||||
| chr4:46791301
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0002g0024a0001c0001t0002g0073others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+53659C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791301 | ||||||
| chr4:46791305
|
A | G | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-50+53655T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791305 | ||||||
| chr4:46791364
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-50+53596T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791364 | ||||||
| chr4:46791518
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53442T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791518 | ||||||
| chr4:46791605
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0280 | 2 | HG00544.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-50+53355A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791605 | ||||||
| chr4:46791750
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0002g0069 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-50+53210A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791750 | ||||||
| chr4:46791812
|
T | A | 4 | a0001c0001t0002g0030a0001c0001t0005g0004a0001c0001t0005g0005others(1): Show | 4 | NA18945.hp2 NA19003.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+53148A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791812 | ||||||
| chr4:46791844
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-50+53116A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791844 | ||||||
| chr4:46791860
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+53100T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791860 | ||||||
| chr4:46791874
|
TG | T | 5 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+53085delC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791874 | ||||||
| chr4:46791967
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52993C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46791967 | ||||||
| chr4:46792002
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52958C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792002 | ||||||
| chr4:46792100
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-50+52860G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792100 | ||||||
| chr4:46792222
|
C | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+52738G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792222 | ||||||
| chr4:46792351
|
G | A | 1 | a0001c0001t0003g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-50+52609C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792351 | ||||||
| chr4:46792368
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-50+52592C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792368 | ||||||
| chr4:46792520
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52440G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792520 | ||||||
| chr4:46792566
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52394G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792566 | ||||||
| chr4:46792617
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52343T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792617 | ||||||
| chr4:46792658
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+52302T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792658 | ||||||
| chr4:46792785
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+52175C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792785 | ||||||
| chr4:46792868
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+52092C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792868 | ||||||
| chr4:46792924
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0065 | 3 | HG02145.hp2 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+52036A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792924 | ||||||
| chr4:46792953
|
A | C | 5 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+52007T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792953 | ||||||
| chr4:46792984
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51976G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792984 | ||||||
| chr4:46792998
|
A | C | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+51962T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46792998 | ||||||
| chr4:46793027
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51933T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793027 | ||||||
| chr4:46793028
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+51932G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793028 | ||||||
| chr4:46793057
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51903A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793057 | ||||||
| chr4:46793105
|
T | A | 6 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+51855A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793105 | ||||||
| chr4:46793179
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51781T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793179 | ||||||
| chr4:46793180
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-50+51780G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793180 | ||||||
| chr4:46793275
|
G | C | 1 | a0001c0001t0003g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-50+51685C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793275 | ||||||
| chr4:46793297
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51663A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793297 | ||||||
| chr4:46793301
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51659C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793301 | ||||||
| chr4:46793310
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51650C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793310 | ||||||
| chr4:46793558
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51402G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793558 | ||||||
| chr4:46793584
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+51376C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793584 | ||||||
| chr4:46793680
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51280C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793680 | ||||||
| chr4:46793727
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51233T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793727 | ||||||
| chr4:46793763
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50+51197C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793763 | ||||||
| chr4:46793841
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51119T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793841 | ||||||
| chr4:46793951
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+51009A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46793951 | ||||||
| chr4:46794038
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+50922T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794038 | ||||||
| chr4:46794046
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-50+50914A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794046 | ||||||
| chr4:46794086
|
A | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+50874T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794086 | ||||||
| chr4:46794113
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+50847T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794113 | ||||||
| chr4:46794299
|
T | A | 5 | a0001c0001t0003g0255a0001c0001t0003g0261a0001c0001t0003g0263others(2): Show | 5 | HG01070.hp2 HG01934.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+50661A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794299 | ||||||
| chr4:46794365
|
A | G | 8 | a0001c0001t0001g0220a0001c0001t0001g0282a0001c0001t0002g0073others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+50595T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794365 | ||||||
| chr4:46794445
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0045 | 2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-50+50515G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794445 | ||||||
| chr4:46794449
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0254 | 3 | HG02056.hp2 NA18954.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-50+50511T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794449 | ||||||
| chr4:46794548
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-50+50412T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794548 | ||||||
| chr4:46794553
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-50+50407G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794553 | ||||||
| chr4:46794741
|
A | G | 7 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+50219T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794741 | ||||||
| chr4:46794812
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+50148T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794812 | ||||||
| chr4:46794819
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(50): Show | 55 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-50+50141T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794819 | ||||||
| chr4:46794866
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+50094G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794866 | ||||||
| chr4:46794983
|
TAAAGGAG others(2131): Show |
T | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+47839_-50+4997 others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46794983 | ||||||
| chr4:46795005
|
A | G | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+49955T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795005 | ||||||
| chr4:46795026
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-50+49934C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795026 | ||||||
| chr4:46795062
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-50+49898A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795062 | ||||||
| chr4:46795119
|
G | A | 1 | a0001c0001t0003g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-50+49841C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795119 | ||||||
| chr4:46795227
|
T | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0177a0001c0001t0001g0216others(2): Show | 5 | HG01256.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+49733A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795227 | ||||||
| chr4:46795419
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-50+49541C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795419 | ||||||
| chr4:46795566
|
T | C | 58 | a0000c0002t0003g0233a0001c0001t0001g0142a0001c0001t0001g0238others(55): Show | 58 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-50+49394A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795566 | ||||||
| chr4:46795800
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50+49160T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795800 | ||||||
| chr4:46795838
|
A | C | 4 | a0001c0001t0003g0225a0001c0001t0003g0229a0001c0001t0003g0242others(1): Show | 4 | HG01358.hp1 HG02148.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+49122T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795838 | ||||||
| chr4:46795897
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-50+49063G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795897 | ||||||
| chr4:46795916
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-50+49044T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795916 | ||||||
| chr4:46795918
|
C | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(4): Show | 7 | HG00642.hp2 HG01243.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+49042G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795918 | ||||||
| chr4:46795923
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-50+49037C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46795923 | ||||||
| chr4:46796107
|
C | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-50+48853G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796107 | ||||||
| chr4:46796107
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-50+48853G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796107 | ||||||
| chr4:46796147
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+48813G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796147 | ||||||
| chr4:46796251
|
G | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-50+48709C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796251 | ||||||
| chr4:46796336
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-50+48624T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796336 | ||||||
| chr4:46796370
|
T | G | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-50+48590A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796370 | ||||||
| chr4:46796433
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-50+48527G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796433 | ||||||
| chr4:46796490
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-50+48470C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796490 | ||||||
| chr4:46796544
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+48416C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796544 | ||||||
| chr4:46796591
|
G | A | 8 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0095others(5): Show | 8 | HG00621.hp1 NA18939.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+48369C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796591 | ||||||
| chr4:46796594
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(50): Show | 55 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-50+48366T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796594 | ||||||
| chr4:46796605
|
T | G | 10 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0095others(7): Show | 10 | HG00621.hp1 HG02738.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+48355A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796605 | ||||||
| chr4:46796608
|
G | C | 10 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0095others(7): Show | 10 | HG00621.hp1 HG02738.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+48352C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796608 | ||||||
| chr4:46796720
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50+48240T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796720 | ||||||
| chr4:46796859
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+48101C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796859 | ||||||
| chr4:46796884
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-50+48076A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796884 | ||||||
| chr4:46796956
|
C | G | 279 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-50+48004G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796956 | ||||||
| chr4:46796998
|
C | T | 114 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(111): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-50+47962G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46796998 | ||||||
| chr4:46797015
|
C | T | 1 | a0002c0003t0001g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+47945G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797015 | ||||||
| chr4:46797024
|
A | G | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+47936T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797024 | ||||||
| chr4:46797064
|
C | A | 1 | a0001c0001t0003g0229 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-50+47896G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797064 | ||||||
| chr4:46797092
|
T | TA | 15 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 15 | HG00621.hp1 HG01175.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-50+47867dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TA | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(25): Show | 29 | HG00280.hp1 HG00609.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-50+47867delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TAA | T | 56 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(53): Show | 57 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-50+47866_-50+4786 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TAAA | T | 44 | a0000c0002t0003g0233a0001c0001t0001g0146a0001c0001t0001g0169others(41): Show | 44 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-50+47865_-50+4786 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TAAAA | T | 7 | a0001c0001t0001g0142a0001c0001t0002g0044a0001c0001t0003g0100others(4): Show | 7 | HG02132.hp2 HG02293.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+47864_-50+4786 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TAAAAAAA others(8): Show |
T | 68 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-50+47853_-50+4786 others(19): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797092
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-50+47852_-50+4786 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797092 | ||||||
| chr4:46797161
|
C | G | 1 | a0001c0001t0003g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-50+47799G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797161 | ||||||
| chr4:46797162
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+47798T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797162 | ||||||
| chr4:46797219
|
G | A | 1 | a0001c0001t0004g0027 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-50+47741C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797219 | ||||||
| chr4:46797226
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+47734C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797226 | ||||||
| chr4:46797322
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-50+47638T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797322 | ||||||
| chr4:46797330
|
G | T | 296 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-50+47630C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797330 | ||||||
| chr4:46797493
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+47467C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797493 | ||||||
| chr4:46797606
|
C | T | 1 | a0001c0001t0003g0235 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-50+47354G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797606 | ||||||
| chr4:46797677
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-50+47283G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46797677 | ||||||
| chr4:46798131
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-50+46829G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798131 | ||||||
| chr4:46798387
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+46573T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798387 | ||||||
| chr4:46798467
|
A | G | 56 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(53): Show | 56 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-50+46493T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798467 | ||||||
| chr4:46798601
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+46359A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798601 | ||||||
| chr4:46798902
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0053 | 2 | NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-50+46058G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798902 | ||||||
| chr4:46798938
|
A | G | 130 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-50+46022T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798938 | ||||||
| chr4:46798938
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-50+46022T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46798938 | ||||||
| chr4:46799115
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+45845C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799115 | ||||||
| chr4:46799136
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50+45824A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799136 | ||||||
| chr4:46799243
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+45717G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799243 | ||||||
| chr4:46799260
|
G | C | 1 | a0001c0001t0003g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-50+45700C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799260 | ||||||
| chr4:46799269
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50+45691C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799269 | ||||||
| chr4:46799326
|
T | C | 1 | a0001c0001t0003g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-50+45634A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799326 | ||||||
| chr4:46799327
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-50+45633G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799327 | ||||||
| chr4:46799574
|
G | A | 32 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+45386C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799574 | ||||||
| chr4:46799590
|
C | T | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+45370G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799590 | ||||||
| chr4:46799676
|
G | GAACT | 8 | a0001c0001t0001g0220a0001c0001t0001g0282a0001c0001t0002g0073others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+45283_-50+4528 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799676 | ||||||
| chr4:46799857
|
C | T | 1 | a0001c0001t0003g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+45103G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799857 | ||||||
| chr4:46799884
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0006g0172 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+45076G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799884 | ||||||
| chr4:46799949
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+45011C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46799949 | ||||||
| chr4:46800018
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0066 | 2 | HG00423.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-50+44942A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800018 | ||||||
| chr4:46800425
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50+44535T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800425 | ||||||
| chr4:46800521
|
T | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0207a0001c0001t0001g0294others(2): Show | 5 | HG02738.hp2 HG03491.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+44439A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800521 | ||||||
| chr4:46800648
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-50+44312A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800648 | ||||||
| chr4:46800758
|
CTTAA | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+44198_-50+4420 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800758 | ||||||
| chr4:46800786
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+44174C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800786 | ||||||
| chr4:46800820
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+44140T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46800820 | ||||||
| chr4:46801027
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-50+43933T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801027 | ||||||
| chr4:46801107
|
G | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0141 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-50+43853C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801107 | ||||||
| chr4:46801231
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0098 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-50+43729C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801231 | ||||||
| chr4:46801329
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+43631C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801329 | ||||||
| chr4:46801348
|
G | A | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+43612C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801348 | ||||||
| chr4:46801350
|
T | C | 4 | a0001c0001t0003g0225a0001c0001t0003g0229a0001c0001t0003g0242others(1): Show | 4 | HG01358.hp1 HG02148.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+43610A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801350 | ||||||
| chr4:46801489
|
A | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+43471T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801489 | ||||||
| chr4:46801499
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-50+43461A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801499 | ||||||
| chr4:46801543
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+43417G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801543 | ||||||
| chr4:46801714
|
T | C | 1 | a0001c0001t0003g0256 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-50+43246A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801714 | ||||||
| chr4:46801792
|
T | C | 4 | a0001c0001t0003g0225a0001c0001t0003g0229a0001c0001t0003g0242others(1): Show | 4 | HG01358.hp1 HG02148.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+43168A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46801792 | ||||||
| chr4:46802413
|
T | C | 56 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(53): Show | 56 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-50+42547A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46802413 | ||||||
| chr4:46802479
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+42481T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46802479 | ||||||
| chr4:46802623
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-50+42337T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46802623 | ||||||
| chr4:46802720
|
G | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+42240C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46802720 | ||||||
| chr4:46802739
|
T | C | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+42221A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46802739 | ||||||
| chr4:46803044
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0006g0172 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+41916C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803044 | ||||||
| chr4:46803065
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+41895A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803065 | ||||||
| chr4:46803239
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+41721T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803239 | ||||||
| chr4:46803327
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+41633A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803327 | ||||||
| chr4:46803330
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50+41630A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803330 | ||||||
| chr4:46803478
|
CAA | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+41480_-50+4148 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803478 | ||||||
| chr4:46803551
|
A | T | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+41409T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803551 | ||||||
| chr4:46803667
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-50+41293C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803667 | ||||||
| chr4:46803685
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+41275A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803685 | ||||||
| chr4:46803732
|
CT | C | 168 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(165): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-50+41227delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803732 | ||||||
| chr4:46803732
|
CTT | C | 18 | a0001c0001t0001g0097a0001c0001t0001g0137a0001c0001t0001g0143others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-50+41226_-50+4122 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803732 | ||||||
| chr4:46803779
|
A | C | 186 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-50+41181T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803779 | ||||||
| chr4:46803813
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-50+41147C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803813 | ||||||
| chr4:46803872
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-50+41088T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803872 | ||||||
| chr4:46803937
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+41023C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803937 | ||||||
| chr4:46803968
|
C | T | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+40992G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803968 | ||||||
| chr4:46803979
|
A | G | 9 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(6): Show | 9 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+40981T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46803979 | ||||||
| chr4:46804053
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+40907A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804053 | ||||||
| chr4:46804109
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0006g0172 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+40851A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804109 | ||||||
| chr4:46804183
|
C | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+40777G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804183 | ||||||
| chr4:46804188
|
G | A | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+40772C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804188 | ||||||
| chr4:46804219
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40741G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804219 | ||||||
| chr4:46804238
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50+40722C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804238 | ||||||
| chr4:46804240
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-50+40720T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804240 | ||||||
| chr4:46804284
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-50+40676C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804284 | ||||||
| chr4:46804288
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+40672C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804288 | ||||||
| chr4:46804297
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-50+40663T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804297 | ||||||
| chr4:46804303
|
C | T | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-50+40657G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804303 | ||||||
| chr4:46804310
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+40650C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804310 | ||||||
| chr4:46804369
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+40591A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804369 | ||||||
| chr4:46804563
|
CAGAGTAG others(2): Show |
C | 5 | a0001c0001t0002g0073a0001c0001t0003g0096a0001c0001t0003g0151others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40388_-50+4039 others(13): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804563 | ||||||
| chr4:46804584
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+40376T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804584 | ||||||
| chr4:46804625
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-50+40335G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804625 | ||||||
| chr4:46804744
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+40216T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804744 | ||||||
| chr4:46804785
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0006g0172 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+40175C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804785 | ||||||
| chr4:46804788
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-50+40172C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804788 | ||||||
| chr4:46804821
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(3): Show | 6 | HG01074.hp1 HG03486.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+40139C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804821 | ||||||
| chr4:46804824
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40136A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804824 | ||||||
| chr4:46804828
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40132A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804828 | ||||||
| chr4:46804842
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40118A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804842 | ||||||
| chr4:46804843
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40117A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804843 | ||||||
| chr4:46804852
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40108A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804852 | ||||||
| chr4:46804861
|
T | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40099A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804861 | ||||||
| chr4:46804865
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40095G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804865 | ||||||
| chr4:46804866
|
A | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+40094T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804866 | ||||||
| chr4:46804883
|
T | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0037a0001c0001t0004g0027 | 3 | HG02083.hp1 NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-50+40077A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804883 | ||||||
| chr4:46804962
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+39998G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804962 | ||||||
| chr4:46804979
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-50+39981G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804979 | ||||||
| chr4:46804980
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+39980C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46804980 | ||||||
| chr4:46805001
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-50+39959G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805001 | ||||||
| chr4:46805012
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0002g0061 | 2 | HG01257.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-50+39948G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805012 | ||||||
| chr4:46805064
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+39896G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805064 | ||||||
| chr4:46805123
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+39837C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805123 | ||||||
| chr4:46805141
|
C | T | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+39819G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805141 | ||||||
| chr4:46805143
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+39817C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805143 | ||||||
| chr4:46805164
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+39796A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805164 | ||||||
| chr4:46805180
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50+39780G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805180 | ||||||
| chr4:46805261
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-50+39699T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805261 | ||||||
| chr4:46805295
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+39665G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805295 | ||||||
| chr4:46805307
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0065 | 3 | HG02145.hp2 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+39653C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805307 | ||||||
| chr4:46805340
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-50+39620G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805340 | ||||||
| chr4:46805484
|
C | T | 17 | a0001c0001t0001g0092a0001c0001t0001g0123a0001c0001t0001g0147others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-50+39476G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805484 | ||||||
| chr4:46805594
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+39366A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805594 | ||||||
| chr4:46805633
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+39327C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805633 | ||||||
| chr4:46805739
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-50+39221C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805739 | ||||||
| chr4:46805739
|
G | T | 1 | a0002c0003t0001g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+39221C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805739 | ||||||
| chr4:46805843
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-50+39117G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805843 | ||||||
| chr4:46805953
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50+39007A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805953 | ||||||
| chr4:46805979
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+38981A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46805979 | ||||||
| chr4:46806224
|
T | C | 1 | a0001c0001t0003g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-50+38736A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46806224 | ||||||
| chr4:46806316
|
T | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+38644A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46806316 | ||||||
| chr4:46807043
|
A | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+37917T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807043 | ||||||
| chr4:46807095
|
C | CT | 16 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(13): Show | 16 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+37864dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807095 | ||||||
| chr4:46807218
|
T | A | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+37742A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807218 | ||||||
| chr4:46807292
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+37668A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807292 | ||||||
| chr4:46807413
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50+37547G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807413 | ||||||
| chr4:46807490
|
A | C | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-50+37470T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807490 | ||||||
| chr4:46807778
|
G | C | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-50+37182C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807778 | ||||||
| chr4:46807854
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-50+37106C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807854 | ||||||
| chr4:46807885
|
T | A | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+37075A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807885 | ||||||
| chr4:46807963
|
A | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+36997T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46807963 | ||||||
| chr4:46808041
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-50+36919C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808041 | ||||||
| chr4:46808107
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+36853A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808107 | ||||||
| chr4:46808116
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-50+36844A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808116 | ||||||
| chr4:46808116
|
T | G | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-50+36844A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808116 | ||||||
| chr4:46808135
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50+36825A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808135 | ||||||
| chr4:46808191
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0191 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-50+36769T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808191 | ||||||
| chr4:46808222
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0213 | 2 | NA19003.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-50+36738C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808222 | ||||||
| chr4:46808291
|
G | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+36669C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808291 | ||||||
| chr4:46808402
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-50+36558A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808402 | ||||||
| chr4:46808501
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-50+36459T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808501 | ||||||
| chr4:46808628
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0254 | 3 | HG02056.hp2 NA18954.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-50+36332C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808628 | ||||||
| chr4:46808714
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+36246T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808714 | ||||||
| chr4:46808783
|
T | C | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+36177A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808783 | ||||||
| chr4:46808847
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+36113C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808847 | ||||||
| chr4:46808883
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-50+36077A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808883 | ||||||
| chr4:46808956
|
C | A | 111 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0097others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-50+36004G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808956 | ||||||
| chr4:46808991
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+35969G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46808991 | ||||||
| chr4:46809825
|
T | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+35135A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46809825 | ||||||
| chr4:46809884
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-50+35076A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46809884 | ||||||
| chr4:46809942
|
T | A | 1 | a0001c0001t0003g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-50+35018A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46809942 | ||||||
| chr4:46809980
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+34980T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46809980 | ||||||
| chr4:46810075
|
A | G | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+34885T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810075 | ||||||
| chr4:46810311
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-50+34649G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810311 | ||||||
| chr4:46810613
|
C | T | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+34347G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810613 | ||||||
| chr4:46810683
|
C | T | 8 | a0000c0002t0003g0233a0001c0001t0003g0231a0001c0001t0003g0232others(5): Show | 8 | HG02132.hp2 NA18612.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+34277G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810683 | ||||||
| chr4:46810728
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-50+34232G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810728 | ||||||
| chr4:46810793
|
TGAA | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+34164_-50+3416 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810793 | ||||||
| chr4:46810917
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-50+34043A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46810917 | ||||||
| chr4:46811024
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0282 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+33936A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811024 | ||||||
| chr4:46811272
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-50+33688C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811272 | ||||||
| chr4:46811273
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-50+33687C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811273 | ||||||
| chr4:46811501
|
C | T | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+33459G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811501 | ||||||
| chr4:46811669
|
T | C | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+33291A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811669 | ||||||
| chr4:46811681
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+33279C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811681 | ||||||
| chr4:46811726
|
A | C | 131 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-50+33234T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811726 | ||||||
| chr4:46811747
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50+33213G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811747 | ||||||
| chr4:46811782
|
C | G | 31 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0283others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-50+33178G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46811782 | ||||||
| chr4:46812061
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-50+32899G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812061 | ||||||
| chr4:46812100
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0002g0047 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-50+32860T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812100 | ||||||
| chr4:46812273
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18966.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-50+32687T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812273 | ||||||
| chr4:46812370
|
TA | T | 227 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0075others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-50+32589delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812370 | ||||||
| chr4:46812421
|
C | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 12 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+32539G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812421 | ||||||
| chr4:46812434
|
G | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 12 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+32526C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812434 | ||||||
| chr4:46812461
|
C | A | 2 | a0001c0001t0001g0282a0001c0001t0006g0172 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50+32499G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812461 | ||||||
| chr4:46812520
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+32440C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812520 | ||||||
| chr4:46812640
|
G | C | 55 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(52): Show | 55 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.-50+32320C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812640 | ||||||
| chr4:46812666
|
G | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+32294C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812666 | ||||||
| chr4:46812889
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+32071G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812889 | ||||||
| chr4:46812936
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-50+32024G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46812936 | ||||||
| chr4:46813000
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0033 | 2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-50+31960G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813000 | ||||||
| chr4:46813294
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-50+31666T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813294 | ||||||
| chr4:46813437
|
C | T | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+31523G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813437 | ||||||
| chr4:46813701
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+31259T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813701 | ||||||
| chr4:46813802
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+31158G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813802 | ||||||
| chr4:46813811
|
C | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+31149G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813811 | ||||||
| chr4:46813812
|
C | A | 1 | a0001c0001t0003g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-50+31148G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46813812 | ||||||
| chr4:46814024
|
C | G | 1 | a0001c0001t0003g0274 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-50+30936G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814024 | ||||||
| chr4:46814247
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+30713T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814247 | ||||||
| chr4:46814421
|
A | G | 1 | a0001c0001t0005g0004 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-50+30539T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814421 | ||||||
| chr4:46814497
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+30463A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814497 | ||||||
| chr4:46814529
|
TA | T | 9 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0113others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+30430delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814529 | ||||||
| chr4:46814722
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50+30238G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814722 | ||||||
| chr4:46814780
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-50+30180T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814780 | ||||||
| chr4:46814914
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-50+30046C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814914 | ||||||
| chr4:46814952
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-50+30008C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814952 | ||||||
| chr4:46814990
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+29970C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46814990 | ||||||
| chr4:46815014
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+29946G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815014 | ||||||
| chr4:46815047
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0029 | 2 | NA18960.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-50+29913C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815047 | ||||||
| chr4:46815116
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+29844C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815116 | ||||||
| chr4:46815161
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+29799A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815161 | ||||||
| chr4:46815185
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+29775T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815185 | ||||||
| chr4:46815402
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-50+29558A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815402 | ||||||
| chr4:46815512
|
C | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-50+29448G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815512 | ||||||
| chr4:46815586
|
T | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(9): Show | 12 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+29374A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815586 | ||||||
| chr4:46815629
|
T | C | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+29331A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815629 | ||||||
| chr4:46815921
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50+29039G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815921 | ||||||
| chr4:46815939
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+29021T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46815939 | ||||||
| chr4:46816018
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-50+28942A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816018 | ||||||
| chr4:46816049
|
G | T | 1 | a0002c0003t0001g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+28911C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816049 | ||||||
| chr4:46816061
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+28899C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816061 | ||||||
| chr4:46816074
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+28886C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816074 | ||||||
| chr4:46816118
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-50+28842G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816118 | ||||||
| chr4:46816259
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+28701G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816259 | ||||||
| chr4:46816333
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+28627C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816333 | ||||||
| chr4:46816335
|
C | G | 1 | a0001c0001t0005g0006 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-50+28625G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816335 | ||||||
| chr4:46816437
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+28523C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816437 | ||||||
| chr4:46816504
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-50+28456A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816504 | ||||||
| chr4:46816573
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-50+28387G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816573 | ||||||
| chr4:46816634
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+28326A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816634 | ||||||
| chr4:46816761
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+28199T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816761 | ||||||
| chr4:46816762
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+28198C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46816762 | ||||||
| chr4:46817139
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-50+27821A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817139 | ||||||
| chr4:46817192
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+27768C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817192 | ||||||
| chr4:46817256
|
A | T | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50+27704T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817256 | ||||||
| chr4:46817257
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50+27703C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817257 | ||||||
| chr4:46817501
|
C | T | 1 | a0001c0001t0003g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+27459G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817501 | ||||||
| chr4:46817715
|
A | T | 1 | a0001c0001t0003g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-50+27245T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46817715 | ||||||
| chr4:46818048
|
T | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0095others(1): Show | 4 | HG00621.hp1 NA18943.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+26912A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818048 | ||||||
| chr4:46818313
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-50+26647A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818313 | ||||||
| chr4:46818415
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+26545A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818415 | ||||||
| chr4:46818479
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-50+26481T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818479 | ||||||
| chr4:46818480
|
C | CA | 6 | a0001c0001t0002g0073a0001c0001t0003g0096a0001c0001t0003g0151others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+26479dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818480 | ||||||
| chr4:46818505
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-50+26455G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818505 | ||||||
| chr4:46818507
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-50+26453T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818507 | ||||||
| chr4:46818636
|
C | CA | 15 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(12): Show | 15 | HG01261.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+26323dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818636 | ||||||
| chr4:46818674
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02040.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-50+26286C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818674 | ||||||
| chr4:46818714
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-50+26246A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46818714 | ||||||
| chr4:46819001
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+25959T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819001 | ||||||
| chr4:46819043
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-50+25917G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819043 | ||||||
| chr4:46819077
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+25883C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819077 | ||||||
| chr4:46819265
|
C | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0223 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-50+25695G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819265 | ||||||
| chr4:46819292
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+25668G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819292 | ||||||
| chr4:46819458
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-50+25502G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819458 | ||||||
| chr4:46819491
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-50+25469A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819491 | ||||||
| chr4:46819539
|
T | TA | 64 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0140others(61): Show | 64 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-50+25420dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819539 | ||||||
| chr4:46819539
|
TA | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0216a0001c0001t0002g0014others(3): Show | 6 | HG00423.hp2 HG01257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+25420delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819539 | ||||||
| chr4:46819539
|
TAA | T | 7 | a0001c0001t0001g0220a0001c0001t0002g0073a0001c0001t0003g0096others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+25419_-50+2542 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819539 | ||||||
| chr4:46819584
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+25376C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819584 | ||||||
| chr4:46819821
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+25139A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819821 | ||||||
| chr4:46819987
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+24973T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819987 | ||||||
| chr4:46819992
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+24968T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46819992 | ||||||
| chr4:46820008
|
G | A | 6 | a0001c0001t0002g0073a0001c0001t0003g0096a0001c0001t0003g0151others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+24952C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820008 | ||||||
| chr4:46820026
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+24934C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820026 | ||||||
| chr4:46820054
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-50+24906G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820054 | ||||||
| chr4:46820220
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+24740C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820220 | ||||||
| chr4:46820401
|
C | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+24559G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820401 | ||||||
| chr4:46820647
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-50+24313G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820647 | ||||||
| chr4:46820743
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+24217G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820743 | ||||||
| chr4:46820818
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-50+24142A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820818 | ||||||
| chr4:46820832
|
A | AAT | 6 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0195others(3): Show | 6 | HG01074.hp2 HG01243.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+24127_-50+2412 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820832 | ||||||
| chr4:46820832
|
A | AT | 4 | a0001c0001t0001g0079a0001c0001t0001g0214a0001c0001t0001g0280others(1): Show | 4 | HG00544.hp2 HG01243.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+24127_-50+2412 others(5): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820832 | ||||||
| chr4:46820832
|
A | T | 19 | a0001c0001t0001g0080a0001c0001t0001g0140a0001c0001t0001g0147others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+24128T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820832 | ||||||
| chr4:46820834
|
A | T | 157 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-50+24126T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820834 | ||||||
| chr4:46820835
|
AT | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0003g0279 | 3 | HG01167.hp1 HG02622.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-50+24124delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820835 | ||||||
| chr4:46820835
|
ATAT | A | 9 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(6): Show | 9 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+24122_-50+2412 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820835 | ||||||
| chr4:46820836
|
T | A | 60 | a0000c0002t0003g0233a0001c0001t0001g0121a0001c0001t0001g0142others(57): Show | 60 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-50+24124A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820836 | ||||||
| chr4:46820838
|
T | A | 58 | a0000c0002t0003g0233a0001c0001t0001g0138a0001c0001t0001g0139others(55): Show | 58 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-50+24122A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820838 | ||||||
| chr4:46820840
|
T | A | 28 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(25): Show | 28 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+24120A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820840 | ||||||
| chr4:46820846
|
T | TAGATAGA others(7): Show |
1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+24113_-50+2411 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820846 | ||||||
| chr4:46820850
|
T | G | 13 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0119others(10): Show | 13 | HG00735.hp1 HG01074.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+24110A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820850 | ||||||
| chr4:46820854
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-50+24106C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820854 | ||||||
| chr4:46820981
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23979G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46820981 | ||||||
| chr4:46821237
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-50+23723C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821237 | ||||||
| chr4:46821296
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23664G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821296 | ||||||
| chr4:46821304
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23656T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821304 | ||||||
| chr4:46821399
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-50+23561G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821399 | ||||||
| chr4:46821400
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+23560A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821400 | ||||||
| chr4:46821465
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23495A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821465 | ||||||
| chr4:46821584
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23376G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821584 | ||||||
| chr4:46821617
|
A | C | 55 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(52): Show | 55 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.-50+23343T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821617 | ||||||
| chr4:46821618
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23342G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821618 | ||||||
| chr4:46821717
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+23243T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821717 | ||||||
| chr4:46821857
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+23103C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821857 | ||||||
| chr4:46821892
|
T | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+23068A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821892 | ||||||
| chr4:46821906
|
TTTTG | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+23050_-50+2305 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46821906 | ||||||
| chr4:46822023
|
T | C | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+22937A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822023 | ||||||
| chr4:46822079
|
T | G | 6 | a0001c0001t0002g0073a0001c0001t0003g0096a0001c0001t0003g0151others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+22881A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822079 | ||||||
| chr4:46822102
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+22858C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822102 | ||||||
| chr4:46822102
|
G | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | NA18941.hp2 NA18957.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+22858C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822102 | ||||||
| chr4:46822191
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+22769C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822191 | ||||||
| chr4:46822224
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+22736T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822224 | ||||||
| chr4:46822380
|
T | TA | 56 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(53): Show | 56 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-50+22579dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822380 | ||||||
| chr4:46822389
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+22571T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822389 | ||||||
| chr4:46822466
|
T | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0037a0001c0001t0004g0027 | 3 | HG02083.hp1 NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-50+22494A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822466 | ||||||
| chr4:46822718
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-50+22242T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822718 | ||||||
| chr4:46822759
|
G | T | 5 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+22201C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46822759 | ||||||
| chr4:46823162
|
T | A | 134 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-50+21798A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823162 | ||||||
| chr4:46823178
|
G | A | 54 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(51): Show | 54 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.-50+21782C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823178 | ||||||
| chr4:46823205
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+21755T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823205 | ||||||
| chr4:46823217
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-50+21743C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823217 | ||||||
| chr4:46823404
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50+21556A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823404 | ||||||
| chr4:46823511
|
A | T | 1 | a0001c0001t0003g0175 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+21449T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823511 | ||||||
| chr4:46823569
|
T | TATA | 31 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(28): Show | 33 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50+21388_-50+2139 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823569 | ||||||
| chr4:46823722
|
C | T | 45 | a0000c0002t0003g0233a0001c0001t0001g0238a0001c0001t0001g0249others(42): Show | 45 | HG00140.hp2 HG00621.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-50+21238G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46823722 | ||||||
| chr4:46824184
|
C | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+20776G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824184 | ||||||
| chr4:46824297
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG03579.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-50+20663G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824297 | ||||||
| chr4:46824327
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0211 | 2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-50+20633T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824327 | ||||||
| chr4:46824354
|
A | G | 11 | a0001c0001t0001g0123a0001c0001t0001g0276a0001c0001t0003g0144others(8): Show | 11 | HG00099.hp2 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+20606T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824354 | ||||||
| chr4:46824358
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+20602T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824358 | ||||||
| chr4:46824654
|
T | TA | 127 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0086others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-50+20305dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824654 | ||||||
| chr4:46824747
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-50+20213T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824747 | ||||||
| chr4:46824779
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+20181T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824779 | ||||||
| chr4:46824922
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+20038C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824922 | ||||||
| chr4:46824935
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+20025C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824935 | ||||||
| chr4:46824941
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-50+20019G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46824941 | ||||||
| chr4:46825050
|
G | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+19910C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825050 | ||||||
| chr4:46825105
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-50+19855C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825105 | ||||||
| chr4:46825129
|
A | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+19831T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825129 | ||||||
| chr4:46825303
|
T | G | 1 | a0001c0001t0003g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-50+19657A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825303 | ||||||
| chr4:46825322
|
C | G | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-50+19638G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825322 | ||||||
| chr4:46825522
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0002g0024 | 2 | HG01123.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-50+19438T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825522 | ||||||
| chr4:46825624
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+19336A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825624 | ||||||
| chr4:46825690
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+19270C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825690 | ||||||
| chr4:46825789
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+19171G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825789 | ||||||
| chr4:46825804
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0003g0255 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-50+19156G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46825804 | ||||||
| chr4:46826093
|
C | T | 35 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-50+18867G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826093 | ||||||
| chr4:46826115
|
T | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+18845A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826115 | ||||||
| chr4:46826176
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+18784T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826176 | ||||||
| chr4:46826261
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+18699T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826261 | ||||||
| chr4:46826320
|
T | C | 35 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-50+18640A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826320 | ||||||
| chr4:46826483
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+18477G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826483 | ||||||
| chr4:46826501
|
C | A | 57 | a0000c0002t0003g0233a0001c0001t0001g0123a0001c0001t0001g0238others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-50+18459G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826501 | ||||||
| chr4:46826561
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(24): Show | 29 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.-50+18399C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826561 | ||||||
| chr4:46826925
|
G | C | 1 | a0001c0001t0002g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-50+18035C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46826925 | ||||||
| chr4:46827085
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+17875T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827085 | ||||||
| chr4:46827095
|
G | A | 6 | a0001c0001t0003g0176a0001c0001t0003g0235a0001c0001t0003g0245others(3): Show | 6 | HG01346.hp2 HG01934.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+17865C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827095 | ||||||
| chr4:46827322
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+17638C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827322 | ||||||
| chr4:46827501
|
T | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+17459A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827501 | ||||||
| chr4:46827619
|
G | A | 2 | a0001c0001t0002g0040a0001c0001t0002g0066 | 2 | HG00423.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-50+17341C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827619 | ||||||
| chr4:46827652
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-50+17308C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827652 | ||||||
| chr4:46827974
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+16986A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46827974 | ||||||
| chr4:46828007
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+16953G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828007 | ||||||
| chr4:46828085
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+16875T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828085 | ||||||
| chr4:46828651
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-50+16309A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828651 | ||||||
| chr4:46828662
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(27): Show | 32 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+16298G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828662 | ||||||
| chr4:46828687
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+16273G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828687 | ||||||
| chr4:46828870
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+16090A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46828870 | ||||||
| chr4:46829100
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0069 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-50+15860G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829100 | ||||||
| chr4:46829186
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+15774A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829186 | ||||||
| chr4:46829453
|
A | G | 3 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0052 | 4 | NA18955.hp1 NA19011.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+15507T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829453 | ||||||
| chr4:46829460
|
A | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+15500T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829460 | ||||||
| chr4:46829510
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+15450C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829510 | ||||||
| chr4:46829574
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-50+15386C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829574 | ||||||
| chr4:46829797
|
AG | A | 5 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0018others(2): Show | 5 | HG02165.hp2 NA18943.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+15162delC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829797 | ||||||
| chr4:46829866
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+15094A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46829866 | ||||||
| chr4:46830048
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14912C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830048 | ||||||
| chr4:46830119
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14841A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830119 | ||||||
| chr4:46830149
|
C | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0289a0001c0001t0001g0293 | 3 | NA18950.hp2 NA18952.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-50+14811G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830149 | ||||||
| chr4:46830166
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-50+14794T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830166 | ||||||
| chr4:46830180
|
C | T | 1 | a0001c0001t0003g0185 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-50+14780G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830180 | ||||||
| chr4:46830181
|
G | A | 9 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(6): Show | 9 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+14779C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830181 | ||||||
| chr4:46830288
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+14672G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830288 | ||||||
| chr4:46830324
|
CA | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-50+14635delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830324 | ||||||
| chr4:46830338
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0186a0001c0001t0001g0211others(1): Show | 4 | HG00738.hp1 HG01433.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+14622T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830338 | ||||||
| chr4:46830340
|
A | G | 2 | a0001c0001t0004g0027a0001c0001t0007g0239 | 2 | NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-50+14620T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830340 | ||||||
| chr4:46830367
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-50+14593C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830367 | ||||||
| chr4:46830379
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+14581A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830379 | ||||||
| chr4:46830545
|
A | C | 201 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-50+14415T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830545 | ||||||
| chr4:46830627
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+14333A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830627 | ||||||
| chr4:46830692
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14268C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830692 | ||||||
| chr4:46830810
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14150G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830810 | ||||||
| chr4:46830906
|
T | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14054A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830906 | ||||||
| chr4:46830907
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+14053C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830907 | ||||||
| chr4:46830909
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-50+14051G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830909 | ||||||
| chr4:46830921
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-50+14039C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830921 | ||||||
| chr4:46830923
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+14037G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830923 | ||||||
| chr4:46830929
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(23): Show | 28 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+14031G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830929 | ||||||
| chr4:46830940
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-50+14020C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830940 | ||||||
| chr4:46830978
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0186a0001c0001t0001g0211others(1): Show | 4 | HG00738.hp1 HG01433.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+13982C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830978 | ||||||
| chr4:46830991
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-50+13969C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46830991 | ||||||
| chr4:46831017
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-50+13943G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831017 | ||||||
| chr4:46831027
|
G | C | 94 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-50+13933C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831027 | ||||||
| chr4:46831132
|
A | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0140others(2): Show | 5 | HG03486.hp2 HG03579.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+13828T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831132 | ||||||
| chr4:46831143
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-50+13817C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831143 | ||||||
| chr4:46831157
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+13803C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831157 | ||||||
| chr4:46831178
|
C | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+13782G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831178 | ||||||
| chr4:46831223
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0002g0010 | 2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-50+13737G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831223 | ||||||
| chr4:46831277
|
C | G | 94 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-50+13683G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831277 | ||||||
| chr4:46831284
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+13676C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831284 | ||||||
| chr4:46831358
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-50+13602C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831358 | ||||||
| chr4:46831383
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+13577G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831383 | ||||||
| chr4:46831480
|
C | T | 1 | a0001c0001t0003g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-50+13480G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831480 | ||||||
| chr4:46831522
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+13438C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831522 | ||||||
| chr4:46831713
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+13247A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831713 | ||||||
| chr4:46831903
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-50+13057T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46831903 | ||||||
| chr4:46832054
|
A | G | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(1): Show | 4 | HG02109.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+12906T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832054 | ||||||
| chr4:46832134
|
C | T | 26 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0097others(23): Show | 27 | HG02040.hp2 HG02056.hp2 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50+12826G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832134 | ||||||
| chr4:46832200
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+12760A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832200 | ||||||
| chr4:46832328
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0006g0172 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-50+12632T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832328 | ||||||
| chr4:46832377
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50+12583A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832377 | ||||||
| chr4:46832649
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-50+12311C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832649 | ||||||
| chr4:46832755
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-50+12205C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832755 | ||||||
| chr4:46832785
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-50+12175G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832785 | ||||||
| chr4:46832791
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+12169C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832791 | ||||||
| chr4:46832792
|
T | C | 1 | a0001c0001t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-50+12168A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832792 | ||||||
| chr4:46832862
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(23): Show | 28 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+12098A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832862 | ||||||
| chr4:46832904
|
C | CT | 34 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0083others(31): Show | 36 | HG01167.hp1 HG01257.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.-50+12055dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832904 | ||||||
| chr4:46832946
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+12014G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832946 | ||||||
| chr4:46832966
|
C | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+11994G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46832966 | ||||||
| chr4:46833288
|
C | T | 1 | a0001c0001t0003g0185 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-50+11672G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833288 | ||||||
| chr4:46833508
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-50+11452C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833508 | ||||||
| chr4:46833511
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+11449A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833511 | ||||||
| chr4:46833595
|
G | T | 7 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+11365C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833595 | ||||||
| chr4:46833657
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+11303A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833657 | ||||||
| chr4:46833807
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+11153T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833807 | ||||||
| chr4:46833941
|
G | T | 15 | a0001c0001t0001g0092a0001c0001t0001g0147a0001c0001t0001g0153others(12): Show | 15 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+11019C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833941 | ||||||
| chr4:46833986
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+10974C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46833986 | ||||||
| chr4:46834197
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-50+10763T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834197 | ||||||
| chr4:46834312
|
T | C | 58 | a0000c0002t0003g0233a0001c0001t0001g0123a0001c0001t0001g0134others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-50+10648A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834312 | ||||||
| chr4:46834491
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50+10469T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834491 | ||||||
| chr4:46834525
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+10435A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834525 | ||||||
| chr4:46834601
|
T | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+10359A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834601 | ||||||
| chr4:46834633
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+10327G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46834633 | ||||||
| chr4:46835076
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+9884C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835076 | ||||||
| chr4:46835103
|
G | T | 2 | a0001c0001t0001g0152a0001c0001t0002g0024 | 2 | HG01123.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-50+9857C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835103 | ||||||
| chr4:46835522
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+9438T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835522 | ||||||
| chr4:46835572
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18982.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-50+9388T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835572 | ||||||
| chr4:46835573
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-50+9387A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835573 | ||||||
| chr4:46835585
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+9375G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835585 | ||||||
| chr4:46835618
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-50+9342T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835618 | ||||||
| chr4:46835745
|
T | C | 31 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0097others(28): Show | 32 | HG01167.hp1 HG02040.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+9215A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835745 | ||||||
| chr4:46835830
|
C | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+9130G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835830 | ||||||
| chr4:46835877
|
G | A | 1 | a0001c0001t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-50+9083C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835877 | ||||||
| chr4:46835953
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+9007A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835953 | ||||||
| chr4:46835995
|
T | G | 1 | a0001c0001t0002g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-50+8965A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46835995 | ||||||
| chr4:46836242
|
C | A | 134 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-50+8718G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836242 | ||||||
| chr4:46836319
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+8641G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836319 | ||||||
| chr4:46836333
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-50+8627A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836333 | ||||||
| chr4:46836334
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+8626A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836334 | ||||||
| chr4:46836353
|
A | T | 4 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+8607T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836353 | ||||||
| chr4:46836353
|
AT | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0082others(3): Show | 6 | HG02145.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+8606delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836353 | ||||||
| chr4:46836354
|
T | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(14): Show | 17 | HG00438.hp1 HG01167.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+8606A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836354 | ||||||
| chr4:46836355
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+8605A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836355 | ||||||
| chr4:46836368
|
T | G | 7 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(4): Show | 7 | HG00642.hp2 HG01243.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+8592A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836368 | ||||||
| chr4:46836406
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-50+8554G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836406 | ||||||
| chr4:46836447
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+8513G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836447 | ||||||
| chr4:46836544
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0002g0065 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-50+8416C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836544 | ||||||
| chr4:46836588
|
AT | A | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+8371delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836588 | ||||||
| chr4:46836592
|
T | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+8368A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836592 | ||||||
| chr4:46836738
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-50+8222G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836738 | ||||||
| chr4:46836969
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+7991A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46836969 | ||||||
| chr4:46837025
|
A | C | 1 | a0001c0001t0003g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+7935T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837025 | ||||||
| chr4:46837053
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+7907T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837053 | ||||||
| chr4:46837234
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-50+7726G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837234 | ||||||
| chr4:46837274
|
T | TAC | 36 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0097others(33): Show | 37 | HG00621.hp1 HG00738.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-50+7684_-50+7685d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
T | TACAC | 11 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0129others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50+7682_-50+7685d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
T | TACACAC | 5 | a0001c0001t0001g0137a0001c0001t0002g0010a0001c0001t0002g0014others(2): Show | 5 | HG01243.hp1 HG01516.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+7680_-50+7685d others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TAC | T | 75 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0123others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-50+7684_-50+7685d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TACAC | T | 26 | a0001c0001t0001g0075a0001c0001t0001g0102a0001c0001t0001g0113others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50+7682_-50+7685d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TACACAC | T | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0115others(12): Show | 15 | HG01123.hp2 HG01261.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+7680_-50+7685d others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+7678_-50+7685d others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-50+7676_-50+7685d others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837274
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0222a0001c0001t0001g0226 | 2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-50+7670_-50+7685d others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837274 | ||||||
| chr4:46837331
|
G | T | 1 | a0001c0001t0003g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-50+7629C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837331 | ||||||
| chr4:46837351
|
G | A | 113 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0083others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-50+7609C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837351 | ||||||
| chr4:46837573
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-50+7387T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837573 | ||||||
| chr4:46837762
|
T | C | 4 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+7198A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837762 | ||||||
| chr4:46837873
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+7087A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46837873 | ||||||
| chr4:46838108
|
A | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+6852T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46838108 | ||||||
| chr4:46838116
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-50+6844C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46838116 | ||||||
| chr4:46838248
|
G | GA | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+6711dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46838248 | ||||||
| chr4:46838710
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-50+6250A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46838710 | ||||||
| chr4:46838927
|
G | A | 94 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.-50+6033C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46838927 | ||||||
| chr4:46839085
|
T | C | 1 | a0001c0001t0003g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-50+5875A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46839085 | ||||||
| chr4:46839175
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+5785C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46839175 | ||||||
| chr4:46839176
|
A | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+5784T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46839176 | ||||||
| chr4:46839177
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+5783C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46839177 | ||||||
| chr4:46839706
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+5254T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46839706 | ||||||
| chr4:46840153
|
T | TG | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0138others(10): Show | 13 | HG01167.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+4806_-50+4807i others(3): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840153 | ||||||
| chr4:46840193
|
A | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0227 | 3 | HG00423.hp1 NA18957.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-50+4767T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840193 | ||||||
| chr4:46840195
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-50+4765T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840195 | ||||||
| chr4:46840406
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-50+4554C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840406 | ||||||
| chr4:46840425
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+4535G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840425 | ||||||
| chr4:46840426
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+4534T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840426 | ||||||
| chr4:46840427
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+4533G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840427 | ||||||
| chr4:46840481
|
TGAGA | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+4475_-50+4478d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840481 | ||||||
| chr4:46840501
|
T | C | 27 | a0001c0001t0001g0092a0001c0001t0001g0137a0001c0001t0001g0147others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-50+4459A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840501 | ||||||
| chr4:46840568
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-50+4392C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840568 | ||||||
| chr4:46840637
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-50+4323C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840637 | ||||||
| chr4:46840813
|
A | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50+4147T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840813 | ||||||
| chr4:46840828
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-50+4132C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840828 | ||||||
| chr4:46840914
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+4046T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840914 | ||||||
| chr4:46840920
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+4040G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840920 | ||||||
| chr4:46840944
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-50+4016G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46840944 | ||||||
| chr4:46841142
|
T | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+3818A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841142 | ||||||
| chr4:46841197
|
G | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50+3763C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841197 | ||||||
| chr4:46841202
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-50+3758C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841202 | ||||||
| chr4:46841335
|
C | CTG | 60 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0086others(57): Show | 62 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.-50+3623_-50+3624d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTG | 20 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0104others(17): Show | 20 | HG00280.hp1 HG01167.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.-50+3621_-50+3624d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTG | 34 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-50+3619_-50+3624d others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTGT others(1): Show |
27 | a0000c0002t0003g0233a0001c0001t0001g0123a0001c0001t0001g0159others(24): Show | 27 | HG00099.hp2 HG01109.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50+3617_-50+3624d others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTGT others(3): Show |
12 | a0001c0001t0001g0220a0001c0001t0001g0249a0001c0001t0001g0250others(9): Show | 12 | HG00438.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50+3615_-50+3624d others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTGT others(5): Show |
7 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0168others(4): Show | 7 | HG02572.hp2 HG03471.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+3613_-50+3624d others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTGT others(7): Show |
5 | a0001c0001t0002g0073a0001c0001t0003g0259a0001c0001t0003g0260others(2): Show | 5 | HG00621.hp2 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+3611_-50+3624d others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0003g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+3607_-50+3624d others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841335
|
CTG | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0204others(3): Show | 6 | HG00621.hp1 HG00735.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+3623_-50+3624d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841335 | ||||||
| chr4:46841416
|
G | C | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(8): Show | 11 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+3544C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841416 | ||||||
| chr4:46841545
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+3415T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841545 | ||||||
| chr4:46841572
|
A | G | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+3388T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841572 | ||||||
| chr4:46841588
|
T | A | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-50+3372A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841588 | ||||||
| chr4:46841596
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+3364G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841596 | ||||||
| chr4:46841622
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+3338T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841622 | ||||||
| chr4:46841756
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+3204T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841756 | ||||||
| chr4:46841769
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+3191C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841769 | ||||||
| chr4:46841832
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+3128A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841832 | ||||||
| chr4:46841940
|
T | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+3020A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46841940 | ||||||
| chr4:46842054
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-50+2906G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842054 | ||||||
| chr4:46842057
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+2903G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842057 | ||||||
| chr4:46842098
|
C | T | 3 | a0001c0001t0003g0228a0001c0001t0003g0241a0001c0001t0003g0258 | 3 | NA18977.hp1 NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-50+2862G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842098 | ||||||
| chr4:46842183
|
C | A | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0138others(10): Show | 13 | HG01167.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+2777G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842183 | ||||||
| chr4:46842301
|
G | C | 5 | a0001c0001t0001g0156a0001c0001t0002g0030a0001c0001t0005g0004others(2): Show | 5 | NA18945.hp2 NA19003.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+2659C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842301 | ||||||
| chr4:46842553
|
C | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+2407G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842553 | ||||||
| chr4:46842557
|
C | G | 1 | a0001c0001t0002g0033 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-50+2403G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842557 | ||||||
| chr4:46842571
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-50+2389A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842571 | ||||||
| chr4:46842576
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-50+2384C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842576 | ||||||
| chr4:46842584
|
A | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+2376T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842584 | ||||||
| chr4:46842693
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+2267A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842693 | ||||||
| chr4:46842709
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0002g0065 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-50+2251A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842709 | ||||||
| chr4:46842824
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50+2136C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46842824 | ||||||
| chr4:46843105
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0213 | 2 | NA19003.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-50+1855C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843105 | ||||||
| chr4:46843128
|
T | A | 1 | a0001c0001t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-50+1832A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843128 | ||||||
| chr4:46843152
|
C | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+1808G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843152 | ||||||
| chr4:46843259
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-50+1701A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843259 | ||||||
| chr4:46843524
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+1436A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843524 | ||||||
| chr4:46843542
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-50+1418T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843542 | ||||||
| chr4:46843720
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-50+1240C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843720 | ||||||
| chr4:46843727
|
G | C | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0082others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-50+1233C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46843727 | ||||||
| chr4:46844009
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-50+951A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844009 | ||||||
| chr4:46844025
|
T | G | 202 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-50+935A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844025 | ||||||
| chr4:46844034
|
T | C | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+926A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844034 | ||||||
| chr4:46844138
|
A | T | 1 | a0001c0001t0003g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-50+822T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844138 | ||||||
| chr4:46844199
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-50+761A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844199 | ||||||
| chr4:46844256
|
T | A | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0138others(10): Show | 13 | HG01167.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+704A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844256 | ||||||
| chr4:46844351
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+609A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844351 | ||||||
| chr4:46844365
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+595T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844365 | ||||||
| chr4:46844773
|
ATCTGTC | A | 5 | a0001c0001t0003g0225a0001c0001t0003g0229a0001c0001t0003g0242others(2): Show | 5 | HG01358.hp1 HG01993.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+181_-50+186del others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844773 | ||||||
| chr4:46844781
|
CTT | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+177_-50+178del others(2): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844781 | ||||||
| chr4:46844791
|
T | C | 9 | a0001c0001t0001g0236a0001c0001t0003g0175a0001c0001t0003g0224others(6): Show | 9 | HG00140.hp2 HG01952.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+169A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844791 | ||||||
| chr4:46844847
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+113T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844847 | ||||||
| chr4:46844916
|
G | C | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-50+44C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844916 | ||||||
| chr4:46844955
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.-50+5C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 2/2 | chr4 | 46844955 | ||||||
| chr4:46845182
|
T | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-104-168A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845182 | ||||||
| chr4:46845312
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-104-298G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845312 | ||||||
| chr4:46845333
|
T | G | 57 | a0000c0002t0003g0233a0001c0001t0001g0123a0001c0001t0001g0236others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-104-319A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845333 | ||||||
| chr4:46845338
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-324G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845338 | ||||||
| chr4:46845421
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-407C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845421 | ||||||
| chr4:46845495
|
T | G | 1 | a0001c0001t0002g0017 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-104-481A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845495 | ||||||
| chr4:46845595
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-581G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845595 | ||||||
| chr4:46845757
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-743G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845757 | ||||||
| chr4:46845772
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-758G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845772 | ||||||
| chr4:46845913
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-899T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845913 | ||||||
| chr4:46845948
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-104-934G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845948 | ||||||
| chr4:46845963
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-104-949C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845963 | ||||||
| chr4:46845984
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-104-970G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845984 | ||||||
| chr4:46845988
|
A | C | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-104-974T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845988 | ||||||
| chr4:46845988
|
A | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-974T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46845988 | ||||||
| chr4:46846154
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-1140C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846154 | ||||||
| chr4:46846421
|
T | G | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-104-1407A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846421 | ||||||
| chr4:46846470
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-1456A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846470 | ||||||
| chr4:46846508
|
G | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-104-1494C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846508 | ||||||
| chr4:46846527
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-1513T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846527 | ||||||
| chr4:46846552
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-104-1538T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846552 | ||||||
| chr4:46846607
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-1593T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846607 | ||||||
| chr4:46846755
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-1741C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46846755 | ||||||
| chr4:46847014
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2000C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847014 | ||||||
| chr4:46847047
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0276 | 2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-104-2033C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847047 | ||||||
| chr4:46847069
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2055T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847069 | ||||||
| chr4:46847073
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-2059G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847073 | ||||||
| chr4:46847075
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-104-2061C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847075 | ||||||
| chr4:46847167
|
CCTT | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-2156_-104-215 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847167 | ||||||
| chr4:46847279
|
A | AG | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2266_-104-226 others(5): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847279 | ||||||
| chr4:46847449
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2435T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847449 | ||||||
| chr4:46847477
|
G | A | 1 | a0001c0001t0003g0248 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-104-2463C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847477 | ||||||
| chr4:46847654
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-2640C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847654 | ||||||
| chr4:46847800
|
C | A | 1 | a0001c0001t0003g0266 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104-2786G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847800 | ||||||
| chr4:46847858
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2844A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847858 | ||||||
| chr4:46847872
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2858C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847872 | ||||||
| chr4:46847919
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2905G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847919 | ||||||
| chr4:46847927
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-2913T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46847927 | ||||||
| chr4:46848053
|
A | AT | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-3040dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848053 | ||||||
| chr4:46848058
|
T | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-3044A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848058 | ||||||
| chr4:46848155
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-3141G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848155 | ||||||
| chr4:46848157
|
A | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-104-3143T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848157 | ||||||
| chr4:46848384
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-3370C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848384 | ||||||
| chr4:46848499
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-3485A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848499 | ||||||
| chr4:46848526
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-104-3512A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848526 | ||||||
| chr4:46848549
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-3535C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848549 | ||||||
| chr4:46848584
|
A | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-3570T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848584 | ||||||
| chr4:46848605
|
A | G | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-104-3591T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848605 | ||||||
| chr4:46848986
|
T | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-3972A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848986 | ||||||
| chr4:46848990
|
T | C | 15 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0091others(12): Show | 16 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-104-3976A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46848990 | ||||||
| chr4:46849111
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-104-4097T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46849111 | ||||||
| chr4:46849320
|
T | A | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-104-4306A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46849320 | ||||||
| chr4:46849514
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-4500A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46849514 | ||||||
| chr4:46849690
|
AT | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0138others(5): Show | 8 | HG01167.hp1 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-4677delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46849690 | ||||||
| chr4:46850003
|
GT | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-4990delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850003 | ||||||
| chr4:46850074
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-5060A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850074 | ||||||
| chr4:46850079
|
A | AAGCAAAA others(5): Show |
6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-5066_-104-506 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850079 | ||||||
| chr4:46850121
|
TTGATTTA others(149): Show |
T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-5263_-104-510 others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850121 | ||||||
| chr4:46850185
|
A | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0223 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-104-5171T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850185 | ||||||
| chr4:46850230
|
TA | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-104-5217delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850230 | ||||||
| chr4:46850311
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-104-5297A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850311 | ||||||
| chr4:46850574
|
C | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-5560G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850574 | ||||||
| chr4:46850675
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-5661C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850675 | ||||||
| chr4:46850705
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-104-5691G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850705 | ||||||
| chr4:46850726
|
C | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0227 | 3 | HG00423.hp1 NA18957.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-104-5712G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850726 | ||||||
| chr4:46850744
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-104-5730C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850744 | ||||||
| chr4:46850773
|
G | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104-5759C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850773 | ||||||
| chr4:46850941
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-5927T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46850941 | ||||||
| chr4:46851019
|
T | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-104-6005A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851019 | ||||||
| chr4:46851052
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-6038C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851052 | ||||||
| chr4:46851197
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 24 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-104-6183A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851197 | ||||||
| chr4:46851227
|
T | C | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-104-6213A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851227 | ||||||
| chr4:46851245
|
A | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-6231T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851245 | ||||||
| chr4:46851250
|
G | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-6236C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851250 | ||||||
| chr4:46851329
|
G | C | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-104-6315C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851329 | ||||||
| chr4:46851426
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-6412A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851426 | ||||||
| chr4:46851575
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-104-6561G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851575 | ||||||
| chr4:46851789
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0006g0106 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-104-6775C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851789 | ||||||
| chr4:46851995
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-104-6981C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46851995 | ||||||
| chr4:46852058
|
A | G | 127 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-104-7044T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852058 | ||||||
| chr4:46852139
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-104-7125A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852139 | ||||||
| chr4:46852155
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-104-7141A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852155 | ||||||
| chr4:46852451
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-104-7437C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852451 | ||||||
| chr4:46852519
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-7505G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852519 | ||||||
| chr4:46852563
|
T | TAC | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0018others(12): Show | 15 | HG01070.hp2 HG01358.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104-7551_-104-755 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852563 | ||||||
| chr4:46852563
|
T | TACAC | 3 | a0001c0001t0001g0220a0001c0001t0002g0065a0001c0001t0003g0151 | 3 | HG02280.hp2 HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-7553_-104-755 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852563 | ||||||
| chr4:46852563
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(1): Show | 4 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-7561_-104-755 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852563 | ||||||
| chr4:46852563
|
T | TACACACA others(7): Show |
2 | a0001c0001t0001g0237a0001c0001t0002g0047 | 2 | HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-104-7563_-104-755 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852563 | ||||||
| chr4:46852637
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-7623G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852637 | ||||||
| chr4:46852720
|
A | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-7706T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852720 | ||||||
| chr4:46852737
|
A | G | 35 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-104-7723T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46852737 | ||||||
| chr4:46853000
|
T | C | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-104-7986A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853000 | ||||||
| chr4:46853217
|
G | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-104-8203C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853217 | ||||||
| chr4:46853241
|
C | A | 5 | a0001c0001t0002g0011a0001c0001t0002g0056a0001c0001t0002g0057others(2): Show | 5 | HG02109.hp1 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104-8227G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853241 | ||||||
| chr4:46853407
|
T | G | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104-8393A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853407 | ||||||
| chr4:46853444
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-8430A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853444 | ||||||
| chr4:46853740
|
A | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-8726T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853740 | ||||||
| chr4:46853756
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-104-8742T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853756 | ||||||
| chr4:46853796
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-104-8782A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46853796 | ||||||
| chr4:46854062
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-104-9048T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854062 | ||||||
| chr4:46854376
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-9362C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854376 | ||||||
| chr4:46854501
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-9487G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854501 | ||||||
| chr4:46854647
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0221 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-104-9633A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854647 | ||||||
| chr4:46854895
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0023a0001c0001t0002g0025others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-9881T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854895 | ||||||
| chr4:46854923
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG01884.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-104-9909A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854923 | ||||||
| chr4:46854936
|
GATT | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-9925_-104-992 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46854936 | ||||||
| chr4:46855043
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-104-10029A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855043 | ||||||
| chr4:46855098
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-10084G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855098 | ||||||
| chr4:46855101
|
G | C | 1 | a0001c0001t0002g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-104-10087C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855101 | ||||||
| chr4:46855404
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0128 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-104-10390T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855404 | ||||||
| chr4:46855420
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-10406C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855420 | ||||||
| chr4:46855547
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-104-10533T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855547 | ||||||
| chr4:46855607
|
C | G | 1 | a0001c0001t0002g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-104-10593G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855607 | ||||||
| chr4:46855642
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-10628C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855642 | ||||||
| chr4:46855667
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-10653A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855667 | ||||||
| chr4:46855863
|
T | G | 4 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-10849A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855863 | ||||||
| chr4:46855970
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-104-10956C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46855970 | ||||||
| chr4:46856016
|
G | T | 2 | a0001c0001t0003g0261a0001c0001t0003g0266 | 2 | NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-104-11002C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856016 | ||||||
| chr4:46856073
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0178 | 3 | HG02809.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-104-11059C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856073 | ||||||
| chr4:46856246
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-104-11232T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856246 | ||||||
| chr4:46856489
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-104-11475G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856489 | ||||||
| chr4:46856542
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-104-11528G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856542 | ||||||
| chr4:46856636
|
G | A | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-104-11622C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856636 | ||||||
| chr4:46856736
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104-11722A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856736 | ||||||
| chr4:46856752
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-11738T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856752 | ||||||
| chr4:46856884
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0223 | 2 | HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-104-11870T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46856884 | ||||||
| chr4:46857193
|
C | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-12179G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46857193 | ||||||
| chr4:46857279
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-104-12265A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46857279 | ||||||
| chr4:46857886
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-104-12872C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46857886 | ||||||
| chr4:46858227
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-104-13213T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858227 | ||||||
| chr4:46858272
|
T | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-13258A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858272 | ||||||
| chr4:46858323
|
T | C | 2 | a0001c0001t0003g0265a0001c0001t0007g0239 | 2 | NA19082.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-104-13309A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858323 | ||||||
| chr4:46858456
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0088 | 2 | HG00621.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-104-13442G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858456 | ||||||
| chr4:46858510
|
GA | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-13497delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858510 | ||||||
| chr4:46858609
|
C | A | 139 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-104-13595G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858609 | ||||||
| chr4:46858716
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-104-13702T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46858716 | ||||||
| chr4:46859015
|
A | G | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-104-14001T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859015 | ||||||
| chr4:46859017
|
C | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-14003G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859017 | ||||||
| chr4:46859062
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-14048T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859062 | ||||||
| chr4:46859080
|
T | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 4 | HG02280.hp2 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-14066A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859080 | ||||||
| chr4:46859157
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-104-14143C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859157 | ||||||
| chr4:46859208
|
T | G | 1 | a0001c0001t0003g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-104-14194A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859208 | ||||||
| chr4:46859435
|
C | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-14421G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859435 | ||||||
| chr4:46859634
|
T | G | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-14620A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859634 | ||||||
| chr4:46859747
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-14733C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859747 | ||||||
| chr4:46859965
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-104-14951C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46859965 | ||||||
| chr4:46860402
|
A | G | 134 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-104-15388T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860402 | ||||||
| chr4:46860435
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-15421G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860435 | ||||||
| chr4:46860591
|
G | T | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-15577C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860591 | ||||||
| chr4:46860777
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02040.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-104-15763G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860777 | ||||||
| chr4:46860809
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-15795T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860809 | ||||||
| chr4:46860817
|
C | T | 200 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-104-15803G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860817 | ||||||
| chr4:46860885
|
A | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0245a0001c0001t0003g0269others(1): Show | 4 | HG01346.hp2 HG01934.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-15871T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46860885 | ||||||
| chr4:46861047
|
A | G | 140 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-104-16033T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861047 | ||||||
| chr4:46861071
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-104-16057C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861071 | ||||||
| chr4:46861083
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-104-16069C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861083 | ||||||
| chr4:46861090
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-104-16076T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861090 | ||||||
| chr4:46861243
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0003g0151a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104-16229A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861243 | ||||||
| chr4:46861246
|
A | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-16232T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861246 | ||||||
| chr4:46861270
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-16256A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861270 | ||||||
| chr4:46861567
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0101others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104-16553A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861567 | ||||||
| chr4:46861593
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-16579A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861593 | ||||||
| chr4:46861682
|
A | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0080others(21): Show | 26 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-104-16668T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861682 | ||||||
| chr4:46861715
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-16701G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861715 | ||||||
| chr4:46861777
|
G | A | 129 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-104-16763C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46861777 | ||||||
| chr4:46862091
|
G | C | 1 | a0001c0001t0002g0044 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-104-17077C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862091 | ||||||
| chr4:46862106
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-104-17092G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862106 | ||||||
| chr4:46862161
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-17147A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862161 | ||||||
| chr4:46862249
|
T | C | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-104-17235A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862249 | ||||||
| chr4:46862300
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-17286G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862300 | ||||||
| chr4:46862453
|
A | G | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-104-17439T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862453 | ||||||
| chr4:46862455
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-104-17441T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862455 | ||||||
| chr4:46862493
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-104-17479G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862493 | ||||||
| chr4:46862565
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-17551C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862565 | ||||||
| chr4:46862730
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-17716C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862730 | ||||||
| chr4:46862804
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0023a0001c0001t0002g0025others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104-17790T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46862804 | ||||||
| chr4:46863094
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-18080G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863094 | ||||||
| chr4:46863234
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-18220A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863234 | ||||||
| chr4:46863498
|
G | A | 2 | a0001c0001t0001g0142a0002c0003t0001g0078 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-104-18484C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863498 | ||||||
| chr4:46863732
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0294 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-104-18718A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863732 | ||||||
| chr4:46863846
|
C | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0227 | 3 | HG00423.hp1 NA18957.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-104-18832G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863846 | ||||||
| chr4:46863921
|
C | A | 1 | a0001c0001t0004g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-104-18907G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46863921 | ||||||
| chr4:46864083
|
C | A | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-104-19069G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864083 | ||||||
| chr4:46864234
|
G | A | 136 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-104-19220C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864234 | ||||||
| chr4:46864257
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-104-19243G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864257 | ||||||
| chr4:46864515
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-104-19501C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864515 | ||||||
| chr4:46864644
|
T | TTTTG | 28 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(25): Show | 30 | HG01167.hp1 HG01257.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.-104-19634_-104-19 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864644 | ||||||
| chr4:46864644
|
T | TTTTGTTT others(1): Show |
79 | a0000c0002t0003g0233a0001c0001t0001g0109a0001c0001t0001g0110others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.-104-19638_-104-19 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864644 | ||||||
| chr4:46864644
|
T | TTTTGTTT others(5): Show |
24 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0146others(21): Show | 24 | HG00280.hp1 HG00639.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.-104-19642_-104-19 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864644 | ||||||
| chr4:46864731
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-104-19717T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864731 | ||||||
| chr4:46864735
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-104-19721G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864735 | ||||||
| chr4:46864793
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-19779C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864793 | ||||||
| chr4:46864933
|
C | T | 35 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-104-19919G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864933 | ||||||
| chr4:46864934
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-19920C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864934 | ||||||
| chr4:46864938
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 4 | HG02280.hp2 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-19924G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864938 | ||||||
| chr4:46864962
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-19948A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46864962 | ||||||
| chr4:46865196
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-20182A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865196 | ||||||
| chr4:46865213
|
C | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0199a0001c0001t0003g0185 | 3 | NA18992.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-104-20199G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865213 | ||||||
| chr4:46865417
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-20403T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865417 | ||||||
| chr4:46865448
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-104-20434G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865448 | ||||||
| chr4:46865634
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-20620C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865634 | ||||||
| chr4:46865651
|
C | G | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-104-20637G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865651 | ||||||
| chr4:46865689
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-104-20675G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865689 | ||||||
| chr4:46865712
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-104-20698C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865712 | ||||||
| chr4:46865713
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-104-20699C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865713 | ||||||
| chr4:46865781
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-104-20767G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865781 | ||||||
| chr4:46865799
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-20785G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46865799 | ||||||
| chr4:46866043
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-104-21029T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866043 | ||||||
| chr4:46866145
|
C | A | 110 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0083others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-104-21131G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866145 | ||||||
| chr4:46866312
|
T | C | 140 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-104-21298A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866312 | ||||||
| chr4:46866317
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-104-21303G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866317 | ||||||
| chr4:46866343
|
C | T | 137 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-104-21329G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866343 | ||||||
| chr4:46866387
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-104-21373C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866387 | ||||||
| chr4:46866486
|
G | A | 95 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-104-21472C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866486 | ||||||
| chr4:46866554
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-21540G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866554 | ||||||
| chr4:46866669
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-21655G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866669 | ||||||
| chr4:46866785
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-104-21771A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866785 | ||||||
| chr4:46866955
|
G | A | 95 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-104-21941C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46866955 | ||||||
| chr4:46867002
|
T | G | 140 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-104-21988A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867002 | ||||||
| chr4:46867003
|
A | G | 5 | a0001c0001t0001g0220a0001c0001t0002g0065a0001c0001t0002g0073others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-21989T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867003 | ||||||
| chr4:46867141
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-22127G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867141 | ||||||
| chr4:46867182
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-104-22168A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867182 | ||||||
| chr4:46867248
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-22234C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867248 | ||||||
| chr4:46867305
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-104-22291A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867305 | ||||||
| chr4:46867386
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-104-22372G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867386 | ||||||
| chr4:46867400
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-104-22386G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867400 | ||||||
| chr4:46867471
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(1): Show | 4 | HG01261.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104-22457C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867471 | ||||||
| chr4:46867555
|
G | A | 201 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-104-22541C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867555 | ||||||
| chr4:46867659
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-104-22645G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867659 | ||||||
| chr4:46867765
|
G | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | NA18950.hp1 NA18961.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-22751C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867765 | ||||||
| chr4:46867813
|
A | G | 141 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-104-22799T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867813 | ||||||
| chr4:46867889
|
C | A | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-104-22875G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46867889 | ||||||
| chr4:46868348
|
G | A | 108 | a0000c0002t0003g0233a0001c0001t0001g0109a0001c0001t0001g0110others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-104-23334C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868348 | ||||||
| chr4:46868465
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-104-23451A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868465 | ||||||
| chr4:46868478
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-23464C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868478 | ||||||
| chr4:46868523
|
C | T | 141 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-104-23509G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868523 | ||||||
| chr4:46868643
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-23629C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868643 | ||||||
| chr4:46868702
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-23688G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46868702 | ||||||
| chr4:46869042
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-104-24028T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46869042 | ||||||
| chr4:46869336
|
G | T | 1 | a0001c0001t0003g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-104-24322C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46869336 | ||||||
| chr4:46869338
|
G | T | 1 | a0001c0001t0003g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-104-24324C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46869338 | ||||||
| chr4:46869498
|
T | G | 1 | a0001c0001t0003g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-104-24484A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46869498 | ||||||
| chr4:46869692
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-104-24678A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46869692 | ||||||
| chr4:46870028
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-104-25014C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870028 | ||||||
| chr4:46870111
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0099others(20): Show | 25 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-104-25097T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870111 | ||||||
| chr4:46870328
|
A | AG | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-25315_-104-25 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870328 | ||||||
| chr4:46870330
|
A | AC | 135 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-104-25317_-104-25 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870330 | ||||||
| chr4:46870330
|
A | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-25316T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870330 | ||||||
| chr4:46870681
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-104-25667G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870681 | ||||||
| chr4:46870851
|
C | T | 16 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0108others(13): Show | 17 | HG02040.hp2 HG02056.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-104-25837G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46870851 | ||||||
| chr4:46871017
|
A | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0080others(22): Show | 27 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-104-26003T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871017 | ||||||
| chr4:46871094
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-104-26080T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871094 | ||||||
| chr4:46871617
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-104-26603T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871617 | ||||||
| chr4:46871639
|
G | GA | 24 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0080others(21): Show | 26 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-104-26626dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871639 | ||||||
| chr4:46871661
|
G | C | 1 | a0001c0001t0001g0155 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-104-26647C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871661 | ||||||
| chr4:46871790
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-104-26776G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871790 | ||||||
| chr4:46871861
|
A | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-26847T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871861 | ||||||
| chr4:46871923
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-104-26909C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871923 | ||||||
| chr4:46871991
|
A | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(3): Show | 6 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104-26977T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46871991 | ||||||
| chr4:46872229
|
C | A | 21 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0108others(18): Show | 22 | HG02040.hp2 HG02056.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-104-27215G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46872229 | ||||||
| chr4:46872343
|
G | A | 139 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-104-27329C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46872343 | ||||||
| chr4:46872394
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-104-27380A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46872394 | ||||||
| chr4:46872771
|
C | T | 134 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-104-27757G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46872771 | ||||||
| chr4:46872852
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-104-27838A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46872852 | ||||||
| chr4:46873093
|
T | A | 142 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-104-28079A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46873093 | ||||||
| chr4:46873273
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128others(7): Show | 10 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-104-28259C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46873273 | ||||||
| chr4:46873394
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-104-28380C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46873394 | ||||||
| chr4:46873968
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0243 | 2 | HG01433.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-104-28954G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46873968 | ||||||
| chr4:46874041
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104-29027G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874041 | ||||||
| chr4:46874137
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-104-29123A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874137 | ||||||
| chr4:46874276
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-104-29262T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874276 | ||||||
| chr4:46874292
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-104-29278G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874292 | ||||||
| chr4:46874542
|
T | A | 98 | a0000c0002t0003g0233a0001c0001t0001g0115a0001c0001t0001g0123others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.-104-29528A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874542 | ||||||
| chr4:46874805
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-104-29791C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874805 | ||||||
| chr4:46874841
|
T | C | 141 | a0000c0002t0003g0233a0001c0001t0001g0002a0001c0001t0001g0079others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-104-29827A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874841 | ||||||
| chr4:46874932
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-104-29918G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874932 | ||||||
| chr4:46874934
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-104-29920C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46874934 | ||||||
| chr4:46875929
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-104-30915A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46875929 | ||||||
| chr4:46875958
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-104-30944A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46875958 | ||||||
| chr4:46876050
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-104-31036A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876050 | ||||||
| chr4:46876081
|
G | C | 1 | a0001c0001t0002g0040 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-104-31067C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876081 | ||||||
| chr4:46876088
|
G | T | 143 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-104-31074C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876088 | ||||||
| chr4:46876109
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-104-31095G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876109 | ||||||
| chr4:46876202
|
G | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-104-31188C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876202 | ||||||
| chr4:46876356
|
GA | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0047others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104-31343delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876356 | ||||||
| chr4:46876404
|
C | CT | 13 | a0001c0001t0001g0075a0001c0001t0001g0125a0001c0001t0001g0137others(10): Show | 13 | HG00140.hp2 HG00673.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104-31391dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876404 | ||||||
| chr4:46876404
|
CT | C | 45 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0128others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-104-31391delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876404 | ||||||
| chr4:46876475
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-104-31461C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876475 | ||||||
| chr4:46876610
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-104-31596C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876610 | ||||||
| chr4:46876695
|
C | T | 1 | a0001c0001t0007g0239 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-104-31681G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876695 | ||||||
| chr4:46876699
|
C | A | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-104-31685G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876699 | ||||||
| chr4:46876701
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-104-31687G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876701 | ||||||
| chr4:46876998
|
T | A | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-104-31984A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46876998 | ||||||
| chr4:46877110
|
T | C | 181 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(178): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-105+32050A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877110 | ||||||
| chr4:46877122
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+32038T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877122 | ||||||
| chr4:46877185
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+31975C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877185 | ||||||
| chr4:46877231
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+31929G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877231 | ||||||
| chr4:46877239
|
G | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+31921C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877239 | ||||||
| chr4:46877253
|
G | A | 1 | a0001c0001t0003g0175 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-105+31907C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877253 | ||||||
| chr4:46877304
|
C | G | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+31856G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877304 | ||||||
| chr4:46877304
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+31856G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877304 | ||||||
| chr4:46877334
|
A | T | 185 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(182): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-105+31826T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877334 | ||||||
| chr4:46877367
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-105+31793G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877367 | ||||||
| chr4:46877422
|
G | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+31738C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877422 | ||||||
| chr4:46877572
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-105+31588C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877572 | ||||||
| chr4:46877675
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02083.hp2 NA18979.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-105+31485A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877675 | ||||||
| chr4:46877772
|
CTGTT | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+31384_-105+31 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877772 | ||||||
| chr4:46877787
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0118others(7): Show | 11 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105+31373A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877787 | ||||||
| chr4:46877964
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0276 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-105+31196T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46877964 | ||||||
| chr4:46878009
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-105+31151T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878009 | ||||||
| chr4:46878020
|
T | TACAC | 65 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0001others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+31136_-105+31 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878020 | ||||||
| chr4:46878103
|
G | A | 1 | a0001c0001t0003g0264 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-105+31057C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878103 | ||||||
| chr4:46878189
|
A | T | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+30971T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878189 | ||||||
| chr4:46878204
|
A | G | 182 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(179): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-105+30956T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878204 | ||||||
| chr4:46878277
|
G | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+30883C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878277 | ||||||
| chr4:46878309
|
A | G | 175 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+30851T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878309 | ||||||
| chr4:46878406
|
T | TA | 6 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG00642.hp1 HG01123.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+30753dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878406 | ||||||
| chr4:46878476
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+30684T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878476 | ||||||
| chr4:46878483
|
T | TTA | 43 | a0000c0002t0003g0233a0001c0001t0001g0200a0001c0001t0001g0238others(40): Show | 44 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.-105+30675_-105+30 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878483 | ||||||
| chr4:46878483
|
TTA | T | 69 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0001others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+30675_-105+30 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878483 | ||||||
| chr4:46878492
|
T | C | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+30668A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878492 | ||||||
| chr4:46878500
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+30660A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878500 | ||||||
| chr4:46878693
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-105+30467C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878693 | ||||||
| chr4:46878892
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+30268G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46878892 | ||||||
| chr4:46879005
|
C | T | 1 | a0001c0001t0002g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-105+30155G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879005 | ||||||
| chr4:46879294
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-105+29866G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879294 | ||||||
| chr4:46879387
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-105+29773C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879387 | ||||||
| chr4:46879410
|
T | A | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-105+29750A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879410 | ||||||
| chr4:46879472
|
C | A | 63 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(60): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-105+29688G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879472 | ||||||
| chr4:46879532
|
TA | T | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+29627delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879532 | ||||||
| chr4:46879541
|
G | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0020 | 3 | HG02165.hp2 NA18943.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-105+29619C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879541 | ||||||
| chr4:46879556
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+29604T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879556 | ||||||
| chr4:46879723
|
C | CA | 65 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(62): Show | 66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+29436dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879723 | ||||||
| chr4:46879733
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-105+29427T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879733 | ||||||
| chr4:46879740
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-105+29420T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879740 | ||||||
| chr4:46879783
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-105+29377C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879783 | ||||||
| chr4:46879976
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+29184C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46879976 | ||||||
| chr4:46880075
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-105+29085A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880075 | ||||||
| chr4:46880258
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+28902C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880258 | ||||||
| chr4:46880340
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+28820C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880340 | ||||||
| chr4:46880410
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-105+28750C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880410 | ||||||
| chr4:46880412
|
C | CT | 57 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0083others(54): Show | 58 | HG00438.hp1 HG00544.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.-105+28747dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880412 | ||||||
| chr4:46880412
|
C | CTT | 8 | a0001c0001t0001g0226a0001c0001t0001g0276a0001c0001t0003g0227others(5): Show | 8 | HG00423.hp1 HG00621.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-105+28746_-105+28 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880412 | ||||||
| chr4:46880412
|
CT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0077others(89): Show | 93 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.-105+28747delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880412 | ||||||
| chr4:46880412
|
CTT | C | 74 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0001g0168others(71): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.-105+28746_-105+28 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880412 | ||||||
| chr4:46880412
|
CTTT | C | 31 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-105+28745_-105+28 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880412 | ||||||
| chr4:46880486
|
T | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+28674A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880486 | ||||||
| chr4:46880491
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+28669C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880491 | ||||||
| chr4:46880595
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-105+28565C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880595 | ||||||
| chr4:46880681
|
T | C | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-105+28479A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880681 | ||||||
| chr4:46880721
|
TA | T | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+28438delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880721 | ||||||
| chr4:46880872
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+28288A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880872 | ||||||
| chr4:46880983
|
T | TA | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+28176dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880983 | ||||||
| chr4:46880993
|
T | A | 1 | a0001c0001t0002g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-105+28167A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAA | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01167.hp1 HG02132.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+28165_-105+28 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAA | 29 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-105+28163_-105+28 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-105+28157_-105+28 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(4): Show |
12 | a0001c0001t0001g0079a0001c0001t0001g0226a0001c0001t0001g0243others(9): Show | 12 | HG01109.hp1 HG01433.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105+28156_-105+28 others(17): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(5): Show |
37 | a0000c0002t0003g0233a0001c0001t0001g0236a0001c0001t0001g0238others(34): Show | 38 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-105+28155_-105+28 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(6): Show |
12 | a0001c0001t0001g0237a0001c0001t0003g0227a0001c0001t0003g0229others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105+28154_-105+28 others(19): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0282a0001c0001t0003g0151 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-105+28152_-105+28 others(21): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(11): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG00642.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-105+28149_-105+28 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+28166_-105+28 others(25): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
T | TAAAAAAA others(14): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01123.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-105+28166_-105+28 others(27): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880993
|
TA | T | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0091others(10): Show | 13 | HG01106.hp1 HG01256.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.-105+28166delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880993 | ||||||
| chr4:46880994
|
A | T | 2 | a0001c0001t0002g0016a0001c0001t0006g0106 | 2 | HG02647.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-105+28166T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46880994 | ||||||
| chr4:46881001
|
A | AAAAATAA others(10): Show |
2 | a0001c0001t0002g0047a0001c0001t0004g0048 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+28158_-105+28 others(23): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881001 | ||||||
| chr4:46881001
|
A | AAAAATAA others(10): Show |
1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+28158_-105+28 others(23): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881001 | ||||||
| chr4:46881008
|
A | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+28152T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881008 | ||||||
| chr4:46881232
|
T | C | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+27928A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881232 | ||||||
| chr4:46881267
|
A | C | 59 | a0000c0002t0003g0233a0001c0001t0001g0226a0001c0001t0001g0236others(56): Show | 60 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-105+27893T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881267 | ||||||
| chr4:46881377
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-105+27783A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881377 | ||||||
| chr4:46881471
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+27689T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881471 | ||||||
| chr4:46881477
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+27683T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881477 | ||||||
| chr4:46881600
|
T | TA | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+27559dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881600 | ||||||
| chr4:46881701
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-105+27459C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881701 | ||||||
| chr4:46881859
|
TCTC | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0047others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+27298_-105+27 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881859 | ||||||
| chr4:46881987
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+27173G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881987 | ||||||
| chr4:46881988
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+27172C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46881988 | ||||||
| chr4:46882183
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-105+26977A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882183 | ||||||
| chr4:46882251
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+26909C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882251 | ||||||
| chr4:46882343
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+26817G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882343 | ||||||
| chr4:46882376
|
A | C | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+26784T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882376 | ||||||
| chr4:46882491
|
A | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG00642.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-105+26669T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882491 | ||||||
| chr4:46882499
|
AG | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+26660delC | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882499 | ||||||
| chr4:46882510
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-105+26650C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882510 | ||||||
| chr4:46882578
|
T | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+26582A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882578 | ||||||
| chr4:46882728
|
T | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(9): Show | 12 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105+26432A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882728 | ||||||
| chr4:46882959
|
A | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0047others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+26201T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46882959 | ||||||
| chr4:46883113
|
G | C | 175 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+26047C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883113 | ||||||
| chr4:46883127
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-105+26033A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883127 | ||||||
| chr4:46883137
|
C | T | 63 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(60): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-105+26023G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883137 | ||||||
| chr4:46883138
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-105+26022C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883138 | ||||||
| chr4:46883321
|
T | C | 1 | a0001c0001t0003g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-105+25839A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883321 | ||||||
| chr4:46883357
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+25803C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883357 | ||||||
| chr4:46883381
|
A | AT | 178 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(175): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-105+25778dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883381 | ||||||
| chr4:46883552
|
A | G | 4 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG00642.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+25608T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883552 | ||||||
| chr4:46883603
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-105+25557A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883603 | ||||||
| chr4:46883755
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+25405G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883755 | ||||||
| chr4:46883776
|
T | TA | 61 | a0000c0002t0003g0233a0001c0001t0001g0136a0001c0001t0001g0226others(58): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-105+25383dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883776 | ||||||
| chr4:46883776
|
TA | T | 38 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-105+25383delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883776 | ||||||
| chr4:46883876
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-105+25284G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883876 | ||||||
| chr4:46883885
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+25275T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883885 | ||||||
| chr4:46883907
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-105+25253A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883907 | ||||||
| chr4:46883991
|
G | C | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+25169C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46883991 | ||||||
| chr4:46884019
|
CAAAT | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG00642.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+25137_-105+25 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884019 | ||||||
| chr4:46884098
|
T | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+25062A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884098 | ||||||
| chr4:46884143
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-105+25017G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884143 | ||||||
| chr4:46884149
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+25011G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884149 | ||||||
| chr4:46884178
|
T | G | 181 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(178): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-105+24982A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884178 | ||||||
| chr4:46884185
|
T | G | 7 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0003g0235others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+24975A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884185 | ||||||
| chr4:46884203
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-105+24957C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884203 | ||||||
| chr4:46884267
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105+24893A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884267 | ||||||
| chr4:46884286
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+24874C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884286 | ||||||
| chr4:46884311
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+24849G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884311 | ||||||
| chr4:46884328
|
A | G | 23 | a0001c0001t0001g0117a0001c0001t0001g0171a0001c0001t0001g0173others(20): Show | 23 | HG01433.hp2 HG01952.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-105+24832T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884328 | ||||||
| chr4:46884424
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+24736C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884424 | ||||||
| chr4:46884559
|
T | C | 184 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(181): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-105+24601A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884559 | ||||||
| chr4:46884619
|
C | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+24541G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884619 | ||||||
| chr4:46884747
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-105+24413A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884747 | ||||||
| chr4:46884787
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-105+24373G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884787 | ||||||
| chr4:46884883
|
C | CT | 9 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0001g0173others(6): Show | 9 | HG01358.hp1 HG01433.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.-105+24276dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884883 | ||||||
| chr4:46884883
|
CT | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+24276delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884883 | ||||||
| chr4:46884984
|
T | C | 182 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(179): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-105+24176A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46884984 | ||||||
| chr4:46885065
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+24095G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885065 | ||||||
| chr4:46885093
|
G | A | 1 | a0001c0001t0003g0279 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-105+24067C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885093 | ||||||
| chr4:46885135
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+24025A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885135 | ||||||
| chr4:46885156
|
T | G | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-105+24004A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885156 | ||||||
| chr4:46885483
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+23677G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885483 | ||||||
| chr4:46885634
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-105+23526G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885634 | ||||||
| chr4:46885687
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+23473C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885687 | ||||||
| chr4:46885704
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+23456C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885704 | ||||||
| chr4:46885729
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0047others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+23431C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46885729 | ||||||
| chr4:46886014
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+23146C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886014 | ||||||
| chr4:46886066
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+23094C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886066 | ||||||
| chr4:46886099
|
A | G | 101 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.-105+23061T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886099 | ||||||
| chr4:46886217
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-105+22943A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886217 | ||||||
| chr4:46886311
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-105+22849A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886311 | ||||||
| chr4:46886518
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-105+22642G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886518 | ||||||
| chr4:46886547
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-105+22613T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886547 | ||||||
| chr4:46886930
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-105+22230A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886930 | ||||||
| chr4:46886955
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-105+22205C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46886955 | ||||||
| chr4:46887323
|
T | A | 207 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-105+21837A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887323 | ||||||
| chr4:46887395
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+21765T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887395 | ||||||
| chr4:46887443
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+21717C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887443 | ||||||
| chr4:46887452
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+21708G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887452 | ||||||
| chr4:46887527
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0034a0001c0001t0002g0046others(1): Show | 4 | HG00140.hp1 HG00280.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+21633G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887527 | ||||||
| chr4:46887571
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0187 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-105+21589G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887571 | ||||||
| chr4:46887604
|
G | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 6 | NA18952.hp1 NA18955.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+21556C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887604 | ||||||
| chr4:46887671
|
A | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+21489T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887671 | ||||||
| chr4:46887710
|
C | CA | 30 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0081others(27): Show | 30 | HG00544.hp1 HG00621.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-105+21449dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887710 | ||||||
| chr4:46887710
|
CA | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0101others(3): Show | 6 | HG01074.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+21449delT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887710 | ||||||
| chr4:46887779
|
T | G | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+21381A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887779 | ||||||
| chr4:46887861
|
T | A | 175 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+21299A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46887861 | ||||||
| chr4:46888029
|
T | C | 2 | a0001c0001t0003g0084a0001c0001t0003g0085 | 2 | NA19000.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-105+21131A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888029 | ||||||
| chr4:46888029
|
T | G | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+21131A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888029 | ||||||
| chr4:46888126
|
C | T | 62 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(59): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-105+21034G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888126 | ||||||
| chr4:46888136
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-105+21024C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888136 | ||||||
| chr4:46888410
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+20750C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888410 | ||||||
| chr4:46888588
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-105+20572G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888588 | ||||||
| chr4:46888639
|
G | A | 2 | a0001c0001t0003g0228a0001c0001t0003g0241 | 2 | NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-105+20521C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888639 | ||||||
| chr4:46888649
|
T | C | 103 | a0000c0002t0003g0233a0001c0001t0001g0145a0001c0001t0001g0146others(100): Show | 104 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-105+20511A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888649 | ||||||
| chr4:46888692
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0022a0001c0001t0002g0023others(3): Show | 6 | HG01243.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+20468G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888692 | ||||||
| chr4:46888737
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-105+20423G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888737 | ||||||
| chr4:46888875
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-105+20285G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46888875 | ||||||
| chr4:46889102
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-105+20058T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889102 | ||||||
| chr4:46889120
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-105+20040T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889120 | ||||||
| chr4:46889143
|
G | GATAA | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(9): Show | 12 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105+20013_-105+20 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889143 | ||||||
| chr4:46889186
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-105+19974T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889186 | ||||||
| chr4:46889571
|
C | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+19589G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889571 | ||||||
| chr4:46889718
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-105+19442A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889718 | ||||||
| chr4:46889779
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+19381C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889779 | ||||||
| chr4:46889893
|
A | G | 184 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(181): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-105+19267T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889893 | ||||||
| chr4:46889899
|
G | GT | 9 | a0001c0001t0001g0116a0001c0001t0001g0173a0001c0001t0001g0194others(6): Show | 9 | HG00438.hp1 HG01261.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.-105+19260dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889899 | ||||||
| chr4:46889899
|
GT | G | 43 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0145others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-105+19260delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889899 | ||||||
| chr4:46889990
|
T | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+19170A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46889990 | ||||||
| chr4:46890188
|
G | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+18972C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890188 | ||||||
| chr4:46890248
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0213 | 2 | NA19003.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-105+18912C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890248 | ||||||
| chr4:46890295
|
C | T | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+18865G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890295 | ||||||
| chr4:46890390
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-105+18770A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890390 | ||||||
| chr4:46890598
|
T | C | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+18562A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890598 | ||||||
| chr4:46890654
|
G | C | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+18506C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890654 | ||||||
| chr4:46890674
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+18486C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890674 | ||||||
| chr4:46890865
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+18295A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890865 | ||||||
| chr4:46890975
|
G | A | 62 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(59): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-105+18185C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46890975 | ||||||
| chr4:46891086
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-105+18074C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891086 | ||||||
| chr4:46891247
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0073a0001c0001t0004g0048 | 3 | HG02451.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-105+17913C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891247 | ||||||
| chr4:46891350
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-105+17810G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891350 | ||||||
| chr4:46891486
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+17674C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891486 | ||||||
| chr4:46891734
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-105+17426C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891734 | ||||||
| chr4:46891749
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+17411G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46891749 | ||||||
| chr4:46892000
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-105+17160A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892000 | ||||||
| chr4:46892002
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+17158C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892002 | ||||||
| chr4:46892020
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+17140G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892020 | ||||||
| chr4:46892024
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+17136G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892024 | ||||||
| chr4:46892123
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+17037C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892123 | ||||||
| chr4:46892181
|
A | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+16979T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892181 | ||||||
| chr4:46892368
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+16792C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892368 | ||||||
| chr4:46892510
|
C | T | 22 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0087others(19): Show | 22 | HG00621.hp1 HG01256.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.-105+16650G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892510 | ||||||
| chr4:46892617
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-105+16543T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892617 | ||||||
| chr4:46892646
|
T | C | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+16514A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892646 | ||||||
| chr4:46892683
|
C | A | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+16477G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892683 | ||||||
| chr4:46892807
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+16353G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892807 | ||||||
| chr4:46892876
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-105+16284C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46892876 | ||||||
| chr4:46893180
|
A | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+15980T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893180 | ||||||
| chr4:46893289
|
C | A | 11 | a0001c0001t0001g0226a0001c0001t0001g0272a0001c0001t0001g0276others(8): Show | 11 | HG01109.hp1 HG01175.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105+15871G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893289 | ||||||
| chr4:46893319
|
T | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+15841A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893319 | ||||||
| chr4:46893325
|
C | T | 1 | a0001c0001t0003g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-105+15835G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893325 | ||||||
| chr4:46893532
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+15628C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893532 | ||||||
| chr4:46893546
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-105+15614G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893546 | ||||||
| chr4:46893570
|
T | C | 1 | a0001c0001t0002g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-105+15590A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893570 | ||||||
| chr4:46893696
|
A | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+15464T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893696 | ||||||
| chr4:46893801
|
C | A | 1 | a0001c0001t0003g0274 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-105+15359G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46893801 | ||||||
| chr4:46894085
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+15075C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894085 | ||||||
| chr4:46894253
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+14907C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894253 | ||||||
| chr4:46894365
|
A | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+14795T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894365 | ||||||
| chr4:46894410
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105+14750T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894410 | ||||||
| chr4:46894411
|
C | T | 71 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0001others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-105+14749G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894411 | ||||||
| chr4:46894412
|
G | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+14748C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894412 | ||||||
| chr4:46894518
|
C | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+14642G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894518 | ||||||
| chr4:46894631
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+14529C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894631 | ||||||
| chr4:46894855
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-105+14305T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894855 | ||||||
| chr4:46894870
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-105+14290T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894870 | ||||||
| chr4:46894885
|
G | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+14275C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46894885 | ||||||
| chr4:46895031
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-105+14129G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895031 | ||||||
| chr4:46895074
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-105+14086G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895074 | ||||||
| chr4:46895122
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+14038G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895122 | ||||||
| chr4:46895202
|
A | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+13958T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895202 | ||||||
| chr4:46895300
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-105+13860G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895300 | ||||||
| chr4:46895328
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-105+13832C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895328 | ||||||
| chr4:46895444
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-105+13716G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895444 | ||||||
| chr4:46895458
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+13702C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895458 | ||||||
| chr4:46895459
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+13701T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895459 | ||||||
| chr4:46895460
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-105+13700C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895460 | ||||||
| chr4:46895574
|
G | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+13586C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895574 | ||||||
| chr4:46895679
|
ATTAT | A | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+13477_-105+13 others(10): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895679 | ||||||
| chr4:46895738
|
A | G | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+13422T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895738 | ||||||
| chr4:46895746
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+13414G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895746 | ||||||
| chr4:46895922
|
A | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+13238T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46895922 | ||||||
| chr4:46896083
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-105+13077A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896083 | ||||||
| chr4:46896113
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-105+13047G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896113 | ||||||
| chr4:46896208
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-105+12952T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896208 | ||||||
| chr4:46896248
|
T | C | 105 | a0000c0002t0003g0233a0001c0001t0001g0145a0001c0001t0001g0146others(102): Show | 106 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-105+12912A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896248 | ||||||
| chr4:46896285
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-105+12875T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896285 | ||||||
| chr4:46896374
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+12786G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896374 | ||||||
| chr4:46896416
|
A | C | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+12744T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896416 | ||||||
| chr4:46896645
|
G | GA | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+12514dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896645 | ||||||
| chr4:46896681
|
T | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0289a0001c0001t0001g0293 | 3 | NA18950.hp2 NA18952.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-105+12479A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896681 | ||||||
| chr4:46896780
|
C | T | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0290others(1): Show | 4 | HG00099.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+12380G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46896780 | ||||||
| chr4:46897002
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+12158A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897002 | ||||||
| chr4:46897059
|
C | G | 1 | a0001c0001t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-105+12101G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897059 | ||||||
| chr4:46897060
|
C | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+12100G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897060 | ||||||
| chr4:46897140
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-105+12020C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897140 | ||||||
| chr4:46897218
|
GCT | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG02451.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+11940_-105+11 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897218 | ||||||
| chr4:46897238
|
C | G | 2 | a0001c0001t0002g0073a0001c0001t0004g0048 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-105+11922G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897238 | ||||||
| chr4:46897367
|
AC | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG03098.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-105+11792delG | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897367 | ||||||
| chr4:46897604
|
T | C | 183 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(180): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-105+11556A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897604 | ||||||
| chr4:46897656
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-105+11504G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897656 | ||||||
| chr4:46897707
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-105+11453A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897707 | ||||||
| chr4:46897814
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+11346C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46897814 | ||||||
| chr4:46898040
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-105+11120G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898040 | ||||||
| chr4:46898148
|
G | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+11012C>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898148 | ||||||
| chr4:46898299
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+10861G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898299 | ||||||
| chr4:46898336
|
T | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+10824A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898336 | ||||||
| chr4:46898483
|
T | C | 1 | a0001c0001t0002g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-105+10677A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898483 | ||||||
| chr4:46898598
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-105+10562A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46898598 | ||||||
| chr4:46899271
|
T | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+9889A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46899271 | ||||||
| chr4:46899366
|
G | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+9794C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46899366 | ||||||
| chr4:46899480
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-105+9680G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46899480 | ||||||
| chr4:46899696
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-105+9464A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46899696 | ||||||
| chr4:46900001
|
T | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+9159A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900001 | ||||||
| chr4:46900158
|
T | A | 1 | a0001c0001t0004g0027 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-105+9002A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900158 | ||||||
| chr4:46900416
|
C | T | 182 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(179): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-105+8744G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900416 | ||||||
| chr4:46900427
|
T | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+8733A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900427 | ||||||
| chr4:46900509
|
G | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+8651C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900509 | ||||||
| chr4:46900617
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-105+8543T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900617 | ||||||
| chr4:46900657
|
T | C | 66 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-105+8503A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900657 | ||||||
| chr4:46900837
|
T | C | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-105+8323A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900837 | ||||||
| chr4:46900950
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-105+8210T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46900950 | ||||||
| chr4:46901104
|
A | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+8056T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901104 | ||||||
| chr4:46901127
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-105+8033A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901127 | ||||||
| chr4:46901188
|
C | A | 1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-105+7972G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901188 | ||||||
| chr4:46901196
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+7964C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901196 | ||||||
| chr4:46901280
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+7880C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901280 | ||||||
| chr4:46901294
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-105+7866G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901294 | ||||||
| chr4:46901335
|
C | G | 175 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+7825G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901335 | ||||||
| chr4:46901474
|
T | C | 9 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0034others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-105+7686A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901474 | ||||||
| chr4:46901555
|
T | A | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-105+7605A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901555 | ||||||
| chr4:46901677
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01074.hp2 HG01256.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+7483C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46901677 | ||||||
| chr4:46902043
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-105+7117T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902043 | ||||||
| chr4:46902127
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-105+7033C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902127 | ||||||
| chr4:46902244
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-105+6916T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902244 | ||||||
| chr4:46902282
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18941.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-105+6878T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902282 | ||||||
| chr4:46902470
|
C | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG00642.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-105+6690G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902470 | ||||||
| chr4:46902813
|
G | A | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+6347C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902813 | ||||||
| chr4:46902821
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+6339C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902821 | ||||||
| chr4:46902899
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0190 | 2 | HG02015.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-105+6261T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46902899 | ||||||
| chr4:46903365
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+5795T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46903365 | ||||||
| chr4:46903459
|
GT | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0082others(3): Show | 6 | HG00423.hp2 HG02145.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+5700delA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46903459 | ||||||
| chr4:46903481
|
T | G | 4 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(1): Show | 4 | HG01070.hp1 HG01123.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+5679A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46903481 | ||||||
| chr4:46903781
|
G | A | 10 | a0001c0001t0002g0031a0001c0001t0002g0040a0001c0001t0002g0041others(7): Show | 10 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.-105+5379C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46903781 | ||||||
| chr4:46903785
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-105+5375T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46903785 | ||||||
| chr4:46904141
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-105+5019T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904141 | ||||||
| chr4:46904315
|
A | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+4845T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904315 | ||||||
| chr4:46904321
|
T | A | 1 | a0001c0001t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-105+4839A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904321 | ||||||
| chr4:46904398
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-105+4762A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904398 | ||||||
| chr4:46904424
|
T | A | 40 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-105+4736A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904424 | ||||||
| chr4:46904681
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-105+4479A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904681 | ||||||
| chr4:46904734
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-105+4426G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904734 | ||||||
| chr4:46904781
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+4379A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904781 | ||||||
| chr4:46904821
|
G | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+4339C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904821 | ||||||
| chr4:46904867
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0112 | 2 | HG02056.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-105+4293T>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46904867 | ||||||
| chr4:46905001
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+4159G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905001 | ||||||
| chr4:46905132
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+4028C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905132 | ||||||
| chr4:46905152
|
G | GT | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+4007dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905152 | ||||||
| chr4:46905194
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-105+3966A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905194 | ||||||
| chr4:46905286
|
C | T | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+3874G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905286 | ||||||
| chr4:46905353
|
T | A | 78 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(75): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-105+3807A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905353 | ||||||
| chr4:46905370
|
G | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+3790C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905370 | ||||||
| chr4:46905400
|
AAACCGGA others(25): Show |
A | 1 | a0001c0001t0003g0275 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-105+3728_-105+375 others(36): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905400 | ||||||
| chr4:46905523
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-105+3637T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905523 | ||||||
| chr4:46905752
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+3408C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905752 | ||||||
| chr4:46905787
|
C | T | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+3373G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905787 | ||||||
| chr4:46905814
|
C | CT | 132 | a0001c0001t0001g0002a0001c0001t0001g0075a0001c0001t0001g0076others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-105+3345dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTT | 31 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0088others(28): Show | 31 | HG00621.hp1 HG00738.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-105+3344_-105+334 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTTTTTTT | 13 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0026others(10): Show | 13 | HG00140.hp2 HG00609.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.-105+3339_-105+334 others(11): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTTTTTTT others(1): Show |
22 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0014others(19): Show | 23 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-105+3338_-105+334 others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTTTTTTT others(2): Show |
14 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0018others(11): Show | 14 | HG00140.hp1 HG00438.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-105+3337_-105+334 others(13): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0002g0017a0001c0001t0002g0031a0001c0001t0002g0041others(3): Show | 6 | HG00423.hp2 HG00673.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-105+3336_-105+334 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0040a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG02132.hp1 NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-105+3335_-105+334 others(15): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905814
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG02970.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-105+3334_-105+334 others(16): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905814 | ||||||
| chr4:46905845
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | NA18941.hp2 NA18957.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+3315G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905845 | ||||||
| chr4:46905942
|
T | G | 185 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(182): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-105+3218A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905942 | ||||||
| chr4:46905954
|
C | G | 107 | a0000c0002t0003g0233a0001c0001t0001g0082a0001c0001t0001g0083others(104): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-105+3206G>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905954 | ||||||
| chr4:46905972
|
G | A | 116 | a0000c0002t0003g0233a0001c0001t0001g0079a0001c0001t0001g0080others(113): Show | 117 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-105+3188C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905972 | ||||||
| chr4:46905984
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-105+3176G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905984 | ||||||
| chr4:46905987
|
G | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0039a0001c0001t0002g0062others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+3173C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46905987 | ||||||
| chr4:46906030
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-105+3130G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906030 | ||||||
| chr4:46906051
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+3109C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906051 | ||||||
| chr4:46906121
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-105+3039T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906121 | ||||||
| chr4:46906187
|
G | C | 63 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(60): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-105+2973C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906187 | ||||||
| chr4:46906219
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-105+2941G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906219 | ||||||
| chr4:46906619
|
A | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+2541T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906619 | ||||||
| chr4:46906633
|
T | C | 1 | a0001c0001t0005g0005 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-105+2527A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46906633 | ||||||
| chr4:46907015
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-105+2145C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907015 | ||||||
| chr4:46907037
|
A | T | 78 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(75): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-105+2123T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907037 | ||||||
| chr4:46907137
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+2023G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907137 | ||||||
| chr4:46907387
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+1773A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907387 | ||||||
| chr4:46907483
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+1677G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907483 | ||||||
| chr4:46907518
|
C | T | 24 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-105+1642G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907518 | ||||||
| chr4:46907561
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-105+1599T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907561 | ||||||
| chr4:46907697
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-105+1463T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907697 | ||||||
| chr4:46907716
|
T | TA | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0154others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-105+1443dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907716 | ||||||
| chr4:46907811
|
G | A | 62 | a0000c0002t0003g0233a0001c0001t0001g0226a0001c0001t0001g0236others(59): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-105+1349C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907811 | ||||||
| chr4:46907824
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-105+1336T>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907824 | ||||||
| chr4:46907848
|
C | CT | 29 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(26): Show | 29 | HG00621.hp1 HG01256.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.-105+1311dupA | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTT | 42 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-105+1310_-105+131 others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTT | 8 | a0001c0001t0001g0079a0001c0001t0001g0142a0001c0001t0001g0145others(5): Show | 8 | HG00642.hp1 HG02572.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.-105+1309_-105+131 others(7): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTT | 49 | a0001c0001t0001g0220a0001c0001t0001g0237a0001c0001t0001g0238others(46): Show | 50 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-105+1308_-105+131 others(8): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTT | 13 | a0000c0002t0003g0233a0001c0001t0001g0226a0001c0001t0001g0236others(10): Show | 13 | HG00423.hp1 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-105+1307_-105+131 others(9): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-105+1298_-105+131 others(18): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-105+1296_-105+131 others(20): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00280.hp2 HG01106.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+1295_-105+131 others(21): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(11): Show |
17 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.-105+1294_-105+131 others(22): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(12): Show |
20 | a0001c0001t0002g0007a0001c0001t0002g0022a0001c0001t0002g0023others(17): Show | 20 | HG00609.hp1 HG00735.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-105+1293_-105+131 others(23): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(13): Show |
8 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(5): Show | 8 | HG00544.hp1 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.-105+1292_-105+131 others(24): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(2): Show | 5 | HG02615.hp2 NA18956.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+1291_-105+131 others(25): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-105+1289_-105+131 others(27): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0010 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-105+1288_-105+131 others(28): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0009 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-105+1311_-105+131 others(31): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907848
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0002g0001a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 6 | NA18952.hp1 NA18955.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-105+1302_-105+131 others(14): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907848 | ||||||
| chr4:46907877
|
C | T | 1 | a0001c0001t0004g0008 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-105+1283G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907877 | ||||||
| chr4:46907956
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+1204G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46907956 | ||||||
| chr4:46908055
|
G | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0137others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105+1105C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908055 | ||||||
| chr4:46908120
|
G | C | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105+1040C>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908120 | ||||||
| chr4:46908214
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+946G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908214 | ||||||
| chr4:46908223
|
A | T | 1 | a0001c0001t0003g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-105+937T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908223 | ||||||
| chr4:46908349
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-105+811G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908349 | ||||||
| chr4:46908355
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-105+805G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908355 | ||||||
| chr4:46908383
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105+777G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908383 | ||||||
| chr4:46908625
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-105+535A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908625 | ||||||
| chr4:46908630
|
T | G | 63 | a0000c0002t0003g0233a0001c0001t0001g0220a0001c0001t0001g0226others(60): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-105+530A>C | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908630 | ||||||
| chr4:46908738
|
C | CA | 90 | a0001c0001t0001g0002a0001c0001t0001g0145a0001c0001t0001g0146others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-105+421dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAA | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01175.hp2 HG01884.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+420_-105+421d others(4): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAAA | 53 | a0000c0002t0003g0233a0001c0001t0001g0226a0001c0001t0001g0236others(50): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-105+419_-105+421d others(5): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAAAA | 7 | a0001c0001t0001g0276a0001c0001t0001g0280a0001c0001t0001g0282others(4): Show | 7 | HG00544.hp2 HG01175.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105+418_-105+421d others(6): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAAAAAAA others(2): Show |
48 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(45): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.-105+413_-105+421d others(11): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAAAAAAA others(3): Show |
16 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(13): Show | 16 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-105+412_-105+421d others(12): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908738
|
C | CAAAAAAA others(4): Show |
5 | a0001c0001t0002g0007a0001c0001t0002g0070a0001c0001t0002g0071others(2): Show | 5 | HG01169.hp1 HG01358.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-105+411_-105+421d others(13): Show |
COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908738 | ||||||
| chr4:46908836
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-105+324A>G | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908836 | ||||||
| chr4:46908843
|
C | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-105+317G>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908843 | ||||||
| chr4:46908969
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+191C>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46908969 | ||||||
| chr4:46909017
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-105+143G>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46909017 | ||||||
| chr4:46909044
|
C | CA | 10 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-105+115dupT | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46909044 | ||||||
| chr4:46909058
|
A | T | 1 | a0001c0001t0002g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-105+102T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46909058 | ||||||
| chr4:46909059
|
A | T | 72 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105+101T>A | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46909059 | ||||||
| chr4:46909060
|
T | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-105+100A>T | COX7B2 | ENSG00000170516.17 | transcript | ENST00000355591.8 | protein_coding | 1/2 | chr4 | 46909060 |