| geneid | 57511 |
|---|---|
| ensemblid | ENSG00000133103.17 |
| hgncid | 18621 |
| symbol | COG6 |
| name | component of oligomeric golgi complex 6 |
| refseq_nuc | NM_020751.3 |
| refseq_prot | NP_065802.1 |
| ensembl_nuc | ENST00000455146.8 |
| ensembl_prot | ENSP00000397441.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 39655662 |
| end | 39752628 |
| strand | + |
| ver | v1.2 |
| region | chr13:39655662-39752628 |
| region5000 | chr13:39650662-39757628 |
| regionname0 | COG6_chr13_39655662_39752628 |
| regionname5000 | COG6_chr13_39650662_39757628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 657 | 215 | 39 | 39 | 99 | 11 | 25 | 81 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002 | 0/0 | 657 | 139 | 39 | 24 | 59 | 7 | 10 | 43 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0003 | 0/0 | 657 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0004 | 0/0 | 657 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0005 | 0/0 | 657 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0007 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0008 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| 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 | 1974 | 211 | 38 | 37 | 98 | 11 | 25 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0002 | 0/0 | 1974 | 138 | 39 | 24 | 58 | 7 | 10 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0003 | 0/0 | 1974 | 6 | 5 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0004 | 0/0 | 1974 | 4 | 1 | 0 | 0 | 0 | 3 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0005 | 0/0 | 1974 | 3 | 3 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0006 | 0/0 | 1974 | 2 | 0 | 2 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0007 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0008 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0009 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0010 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0011 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| c0012 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| 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 | 0/1 | 1601 | 109 | 14 | 19 | 52 | 4 | 19 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0002 | 0/0 | 1601 | 107 | 19 | 21 | 48 | 7 | 12 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0003 | 1/0 | 1601 | 93 | 22 | 20 | 42 | 3 | 5 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0004 | 0/0 | 1600 | 22 | 12 | 0 | 7 | 3 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0005 | 0/0 | 1600 | 11 | 11 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0006 | 0/0 | 1602 | 8 | 2 | 2 | 4 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0007 | 0/0 | 1602 | 5 | 2 | 0 | 2 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0008 | 0/0 | 1601 | 4 | 3 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0009 | 0/0 | 1601 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0010 | 0/0 | 1601 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0011 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0012 | 0/0 | 1601 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0013 | 0/0 | 1601 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0014 | 0/0 | 1601 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| t0015 | 0/0 | 1601 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1974 | 211 | 38 | 37 | 98 | 11 | 25 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0006 | 0/0 | 1974 | 2 | 0 | 2 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0011 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0012 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002 | 0/0 | 1974 | 138 | 39 | 24 | 58 | 7 | 10 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0007 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0003c0003 | 0/0 | 1974 | 6 | 5 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0004c0004 | 0/0 | 1974 | 4 | 1 | 0 | 0 | 0 | 3 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0005c0005 | 0/0 | 1974 | 3 | 3 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0006c0008 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0007c0009 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0008c0010 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3574 | 103 | 9 | 18 | 52 | 4 | 19 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0003 | 1/0 | 3574 | 81 | 13 | 18 | 41 | 3 | 5 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0004 | 0/0 | 3573 | 16 | 8 | 0 | 5 | 3 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0005 | 0/0 | 3573 | 7 | 7 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0012 | 0/0 | 3574 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0013 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0001t0015 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0006t0003 | 0/0 | 3574 | 2 | 0 | 2 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0011t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0001c0012t0003 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0002 | 0/0 | 3574 | 102 | 17 | 21 | 47 | 7 | 10 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0003 | 0/0 | 3574 | 4 | 4 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0004 | 0/0 | 3573 | 6 | 4 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0005 | 0/0 | 3573 | 4 | 4 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0006 | 0/0 | 3575 | 8 | 2 | 2 | 4 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0007 | 0/0 | 3575 | 4 | 2 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0008 | 0/0 | 3574 | 4 | 3 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0009 | 0/0 | 3574 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0010 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0002t0011 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0002c0007t0002 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0003c0003t0001 | 0/0 | 3574 | 6 | 5 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0004c0004t0002 | 0/0 | 3574 | 3 | 1 | 0 | 0 | 0 | 2 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0004c0004t0007 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0005c0005t0003 | 0/0 | 3574 | 3 | 3 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0006c0008t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0007c0009t0010 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| a0008c0010t0002 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | copy fasta | chr13 | 39650662 | 39757628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0013g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0015g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0006t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0006t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0011t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0012t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0011g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0007t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0006c0008t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0007c0009t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0008c0010t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0049 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0104 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0202 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0327 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0313 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00609 | hp1 | a0002 | c0002 | t0006 | g0348 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00639 | hp1 | a0002 | c0002 | t0008 | g0241 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00639 | hp2 | a0001 | c0006 | t0003 | g0041 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0352 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0329 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0293 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0328 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0259 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0322 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0296 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0239 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0350 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0183 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0101 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01255 | hp1 | a0001 | c0006 | t0003 | g0040 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01261 | hp2 | a0002 | c0002 | t0006 | g0231 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0249 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0295 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01433 | hp1 | a0002 | c0002 | t0006 | g0233 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0232 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0324 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0323 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0230 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01884 | hp2 | a0005 | c0005 | t0003 | g0015 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0349 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0177 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02074 | hp1 | a0002 | c0007 | t0002 | g0300 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02083 | hp2 | a0002 | c0002 | t0007 | g0355 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02145 | hp1 | a0002 | c0002 | t0005 | g0219 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0319 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0354 | EAS | CDX | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0310 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0234 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0297 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02451 | hp1 | a0008 | c0010 | t0002 | g0247 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02451 | hp2 | a0002 | c0002 | t0007 | g0330 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02572 | hp1 | a0002 | c0002 | t0007 | g0306 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0216 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0217 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02630 | hp2 | a0005 | c0005 | t0003 | g0016 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0215 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0097 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0331 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0311 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02818 | hp2 | a0001 | c0011 | t0003 | g0210 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0224 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0316 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0225 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02922 | hp1 | a0005 | c0005 | t0003 | g0017 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02965 | hp1 | a0002 | c0002 | t0005 | g0220 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02970 | hp1 | a0002 | c0002 | t0006 | g0321 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0227 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03041 | hp1 | a0002 | c0002 | t0011 | g0012 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0345 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0312 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0317 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0099 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0242 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0169 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03195 | hp2 | a0006 | c0008 | t0003 | g0226 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0337 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0100 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03225 | hp1 | a0004 | c0004 | t0002 | g0254 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0133 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03453 | hp1 | a0002 | c0002 | t0008 | g0243 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0228 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0318 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0304 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03540 | hp1 | a0002 | c0002 | t0005 | g0218 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0308 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03579 | hp1 | a0007 | c0009 | t0010 | g0222 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03579 | hp2 | a0002 | c0002 | t0011 | g0012 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0356 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03688 | hp1 | a0004 | c0004 | t0007 | g0253 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0353 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03927 | hp2 | a0004 | c0004 | t0002 | g0256 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0237 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0351 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0260 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0335 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18939 | hp2 | a0002 | c0002 | t0004 | g0347 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18952 | hp2 | a0002 | c0002 | t0009 | g0277 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18967 | hp1 | a0002 | c0002 | t0006 | g0302 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0332 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19000 | hp2 | a0002 | c0002 | t0009 | g0278 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0343 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19003 | hp2 | a0002 | c0002 | t0004 | g0263 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19007 | hp2 | a0002 | c0002 | t0006 | g0292 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19010 | hp1 | a0001 | c0012 | t0003 | g0073 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19010 | hp2 | a0002 | c0002 | t0009 | g0276 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19030 | hp1 | a0002 | c0002 | t0006 | g0320 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0338 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0309 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0229 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0346 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19077 | hp2 | a0002 | c0002 | t0006 | g0326 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0342 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0336 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0291 | AFR | ASW | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ASW | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0283 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0196 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0236 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0258 | SAS | GIH | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20905 | hp2 | a0004 | c0004 | t0002 | g0255 | SAS | GIH | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0221 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0098 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03471 | hp1 | a0002 | c0002 | t0010 | g0223 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0188 | REF | REF | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655754
|
G | A | 5 | a0002a0004a0006others(2): Show | 146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
missense_variant | MODERATE | c.28G>A | p.Ala10Thr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 93/3574 | 28/1974 | 10/657 | chr13 | 39655754 | ||
| chr13:39655820
|
T | A | 5 | a0002a0004a0006others(2): Show | 146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
missense_variant | MODERATE | c.94T>A | p.Cys32Ser | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 159/3574 | 94/1974 | 32/657 | chr13 | 39655820 | ||
| chr13:39660832
|
A | T | 1 | a0008 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.320A>T | p.Asp107Val | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/19 | 385/3574 | 320/1974 | 107/657 | chr13 | 39660832 | ||
| chr13:39660870
|
A | G | 1 | a0005 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.358A>G | p.Ser120Gly | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/19 | 423/3574 | 358/1974 | 120/657 | chr13 | 39660870 | ||
| chr13:39679982
|
A | C | 1 | a0007 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.631A>C | p.Ile211Leu | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/19 | 696/3574 | 631/1974 | 211/657 | chr13 | 39679982 | ||
| chr13:39687612
|
C | T | 1 | a0003 | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.898C>T | p.His300Tyr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 9/19 | 963/3574 | 898/1974 | 300/657 | chr13 | 39687612 | ||
| chr13:39719291
|
T | C | 1 | a0004 | 4 | HG03225.hp1 HG03688.hp1 HG03927.hp2 others(1): Show |
missense_variant | MODERATE | c.1340T>C | p.Met447Thr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/19 | 1405/3574 | 1340/1974 | 447/657 | chr13 | 39719291 | ||
| chr13:39751082
|
C | A | 1 | a0006 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1963C>A | p.Leu655Ile | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 2028/3574 | 1963/1974 | 655/657 | chr13 | 39751082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39682205
|
C | T | 1 | a0001c0006 | 2 | HG00639.hp2 HG01255.hp1 |
synonymous_variant | LOW | c.729C>T | p.Asp243Asp | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/19 | 794/3574 | 729/1974 | 243/657 | chr13 | 39682205 | ||
| chr13:39687729
|
T | C | 1 | a0002c0007 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.939T>C | p.Ala313Ala | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/19 | 1004/3574 | 939/1974 | 313/657 | chr13 | 39687729 | ||
| chr13:39719259
|
T | G | 1 | a0001c0011 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1308T>G | p.Leu436Leu | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/19 | 1373/3574 | 1308/1974 | 436/657 | chr13 | 39719259 | ||
| chr13:39719668
|
A | G | 1 | a0001c0012 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1425A>G | p.Ser475Ser | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/19 | 1490/3574 | 1425/1974 | 475/657 | chr13 | 39719668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655674
|
T | G | 1 | a0002c0002t0009 | 3 | NA18952.hp2 NA19000.hp2 NA19010.hp2 |
5_prime_UTR_variant | MODIFIER | c.-53T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 53 | chr13 | 39655674 | |||||
| chr13:39655705
|
A | AG | 10 | a0002c0002t0002a0002c0002t0006a0002c0002t0007others(7): Show | 129 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
5_prime_UTR_variant | MODIFIER | c.-17dupG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 16 | INFO_REALIGN_3_PRIME | chr13 | 39655705 | ||||
| chr13:39751133
|
A | G | 1 | a0001c0001t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 40 | chr13 | 39751133 | |||||
| chr13:39751173
|
C | T | 8 | a0001c0001t0004a0002c0002t0002a0002c0002t0004others(5): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 80 | chr13 | 39751173 | |||||
| chr13:39751399
|
AT | A | 2 | a0001c0001t0005a0002c0002t0005 | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*315delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 315 | INFO_REALIGN_3_PRIME | chr13 | 39751399 | ||||
| chr13:39751648
|
G | A | 1 | a0001c0001t0012 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 555 | chr13 | 39751648 | |||||
| chr13:39751682
|
C | G | 1 | a0001c0001t0014 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 589 | chr13 | 39751682 | |||||
| chr13:39751854
|
A | G | 1 | a0001c0001t0013 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 761 | chr13 | 39751854 | |||||
| chr13:39752145
|
A | G | 9 | a0001c0001t0001a0001c0001t0012a0001c0001t0013others(6): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1052 | chr13 | 39752145 | |||||
| chr13:39752147
|
CA | C | 8 | a0001c0001t0004a0002c0002t0002a0002c0002t0004others(5): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1063delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1063 | INFO_REALIGN_3_PRIME | chr13 | 39752147 | ||||
| chr13:39752186
|
G | T | 1 | a0002c0002t0008 | 4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1093G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1093 | chr13 | 39752186 | |||||
| chr13:39752587
|
G | A | 1 | a0002c0002t0011 | 2 | HG03041.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1494G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1494 | chr13 | 39752587 | |||||
| chr13:39752601
|
G | T | 2 | a0002c0002t0010a0007c0009t0010 | 2 | HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1508G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1508 | chr13 | 39752601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655898
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153+19G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655898 | ||||||
| chr13:39655906
|
C | T | 129 | a0002c0002t0002g0011a0002c0002t0002g0230a0002c0002t0002g0232others(126): Show | 131 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.153+27C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655906 | ||||||
| chr13:39655929
|
C | T | 7 | a0002c0002t0002g0350a0002c0002t0002g0351a0002c0002t0002g0352others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+50C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655929 | ||||||
| chr13:39655985
|
A | C | 144 | a0002c0002t0002g0011a0002c0002t0002g0230a0002c0002t0002g0232others(141): Show | 146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.153+106A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655985 | ||||||
| chr13:39655997
|
A | T | 1 | a0002c0002t0002g0349 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153+118A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655997 | ||||||
| chr13:39656079
|
G | A | 145 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(142): Show | 147 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.153+200G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656079 | ||||||
| chr13:39656092
|
C | T | 147 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(144): Show | 149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+213C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656092 | ||||||
| chr13:39656157
|
T | C | 147 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(144): Show | 149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+278T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656157 | ||||||
| chr13:39656228
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.153+349A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656228 | ||||||
| chr13:39656408
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+529C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656408 | ||||||
| chr13:39656568
|
G | A | 147 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(144): Show | 149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+689G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656568 | ||||||
| chr13:39656601
|
A | G | 2 | a0001c0001t0003g0211a0001c0001t0003g0212 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.153+722A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656601 | ||||||
| chr13:39656638
|
A | T | 4 | a0001c0001t0003g0014a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+759A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656638 | ||||||
| chr13:39656799
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153+920C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656799 | ||||||
| chr13:39656803
|
C | T | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.153+924C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656803 | ||||||
| chr13:39656977
|
C | T | 1 | a0002c0002t0004g0347 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.153+1098C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656977 | ||||||
| chr13:39656982
|
A | G | 2 | a0002c0002t0003g0224a0002c0002t0004g0225 | 2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.153+1103A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656982 | ||||||
| chr13:39657023
|
A | T | 1 | a0002c0002t0002g0346 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.153+1144A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657023 | ||||||
| chr13:39657047
|
T | C | 1 | a0006c0008t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.153+1168T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657047 | ||||||
| chr13:39657092
|
C | T | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.153+1213C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657092 | ||||||
| chr13:39657132
|
A | G | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.153+1253A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657132 | ||||||
| chr13:39657157
|
A | G | 147 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(144): Show | 149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+1278A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657157 | ||||||
| chr13:39657354
|
A | C | 1 | a0002c0002t0002g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153+1475A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657354 | ||||||
| chr13:39657463
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+1584T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657463 | ||||||
| chr13:39657530
|
G | GT | 150 | a0001c0001t0001g0208a0001c0001t0003g0014a0001c0001t0003g0207others(147): Show | 152 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.153+1661dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39657530 | |||||
| chr13:39657744
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.154-1620G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657744 | ||||||
| chr13:39657778
|
C | T | 122 | a0002c0002t0002g0011a0002c0002t0002g0238a0002c0002t0002g0239others(119): Show | 124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.154-1586C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657778 | ||||||
| chr13:39657909
|
A | G | 1 | a0002c0002t0002g0344 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.154-1455A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657909 | ||||||
| chr13:39657960
|
C | T | 3 | a0001c0001t0004g0206a0002c0002t0002g0342a0002c0002t0002g0343 | 3 | NA18906.hp1 NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.154-1404C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657960 | ||||||
| chr13:39657970
|
G | C | 16 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(13): Show | 16 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-1394G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657970 | ||||||
| chr13:39658063
|
C | CT | 12 | a0001c0001t0001g0201a0001c0001t0003g0200a0001c0001t0003g0203others(9): Show | 14 | HG00323.hp1 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.154-1283dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658063 | |||||
| chr13:39658063
|
CTT | C | 136 | a0001c0001t0003g0014a0002c0002t0002g0011a0002c0002t0002g0230others(133): Show | 138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.154-1284_154-1283d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658063 | |||||
| chr13:39658103
|
A | T | 1 | a0001c0001t0003g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.154-1261A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658103 | ||||||
| chr13:39658283
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-1081A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658283 | ||||||
| chr13:39658318
|
A | AT | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-1039dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658318 | |||||
| chr13:39658331
|
G | C | 1 | a0002c0002t0002g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154-1033G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658331 | ||||||
| chr13:39658584
|
A | G | 6 | a0002c0002t0002g0336a0002c0002t0002g0337a0002c0002t0002g0338others(3): Show | 6 | HG03041.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-780A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658584 | ||||||
| chr13:39658770
|
A | C | 1 | a0002c0002t0008g0335 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.154-594A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658770 | ||||||
| chr13:39659002
|
A | G | 2 | a0002c0002t0002g0333a0002c0002t0002g0334 | 2 | HG00621.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.154-362A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659002 | ||||||
| chr13:39659044
|
AT | A | 216 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(213): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.154-310delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39659044 | |||||
| chr13:39659157
|
T | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.154-207T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659157 | ||||||
| chr13:39659267
|
T | C | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.154-97T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659267 | ||||||
| chr13:39659273
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.154-91A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659273 | ||||||
| chr13:39659554
|
C | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.297+47C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659554 | ||||||
| chr13:39659829
|
C | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.297+322C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659829 | ||||||
| chr13:39659845
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.297+338A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659845 | ||||||
| chr13:39659891
|
C | T | 1 | a0002c0002t0002g0331 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+384C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659891 | ||||||
| chr13:39659953
|
T | C | 3 | a0002c0002t0002g0350a0002c0002t0002g0351a0002c0002t0002g0352 | 3 | HG00642.hp1 HG01175.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.297+446T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659953 | ||||||
| chr13:39660045
|
C | T | 2 | a0002c0002t0004g0221a0002c0002t0007g0330 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.297+538C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660045 | ||||||
| chr13:39660053
|
T | A | 2 | a0002c0002t0002g0239a0002c0002t0002g0240 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.297+546T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660053 | ||||||
| chr13:39660168
|
C | A | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.298-642C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660168 | ||||||
| chr13:39660187
|
A | T | 4 | a0001c0001t0001g0185a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-623A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660187 | ||||||
| chr13:39660195
|
T | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0088 | 4 | HG00673.hp2 HG02135.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-615T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660195 | ||||||
| chr13:39660281
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG01515.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.298-529G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660281 | ||||||
| chr13:39660296
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-514C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660296 | ||||||
| chr13:39660519
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.298-291G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660519 | ||||||
| chr13:39660657
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-153T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660657 | ||||||
| chr13:39660684
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.298-126G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660684 | ||||||
| chr13:39660713
|
T | G | 4 | a0002c0002t0008g0241a0002c0002t0008g0242a0002c0002t0008g0243others(1): Show | 4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-97T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660713 | ||||||
| chr13:39660809
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG01167.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.298-1G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660809 | ||||||
| chr13:39661048
|
A | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+167A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661048 | ||||||
| chr13:39661198
|
A | G | 1 | a0002c0002t0004g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.369+317A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661198 | ||||||
| chr13:39661236
|
C | T | 209 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(206): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.369+355C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661236 | ||||||
| chr13:39661339
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.369+458A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661339 | ||||||
| chr13:39661542
|
A | G | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0206others(130): Show | 135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.369+661A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661542 | ||||||
| chr13:39661572
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.369+691T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661572 | ||||||
| chr13:39661885
|
T | C | 1 | a0002c0002t0002g0245 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.369+1004T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661885 | ||||||
| chr13:39662075
|
A | G | 1 | a0001c0001t0012g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+1194A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662075 | ||||||
| chr13:39662142
|
A | AT | 9 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0003g0025others(6): Show | 9 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1279dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | |||||
| chr13:39662142
|
A | ATT | 205 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.369+1278_369+1279d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | |||||
| chr13:39662142
|
AT | A | 13 | a0001c0001t0001g0090a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.369+1279delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | |||||
| chr13:39662168
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369+1287A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662168 | ||||||
| chr13:39662221
|
C | G | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0084 | 3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+1340C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662221 | ||||||
| chr13:39662253
|
A | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1372A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662253 | ||||||
| chr13:39662368
|
T | C | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1487T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662368 | ||||||
| chr13:39662414
|
A | T | 1 | a0002c0002t0005g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.369+1533A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662414 | ||||||
| chr13:39662459
|
A | G | 2 | a0002c0002t0003g0224a0002c0002t0004g0225 | 2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+1578A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662459 | ||||||
| chr13:39662464
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1583G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662464 | ||||||
| chr13:39662730
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.369+1849A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662730 | ||||||
| chr13:39662858
|
C | T | 132 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0206others(129): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.369+1977C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662858 | ||||||
| chr13:39662872
|
A | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.369+1991A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662872 | ||||||
| chr13:39662990
|
A | T | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-2106A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662990 | ||||||
| chr13:39663053
|
T | G | 1 | a0001c0001t0004g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-2043T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663053 | ||||||
| chr13:39663080
|
T | C | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370-2016T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663080 | ||||||
| chr13:39663095
|
C | CAT | 215 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(212): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.370-2000_370-1999d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663095 | |||||
| chr13:39663140
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.370-1956T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663140 | ||||||
| chr13:39663372
|
G | T | 1 | a0002c0002t0002g0329 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1724G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663372 | ||||||
| chr13:39663510
|
A | G | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.370-1586A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663510 | ||||||
| chr13:39663531
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.370-1565G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663531 | ||||||
| chr13:39663625
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.370-1471G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663625 | ||||||
| chr13:39663758
|
C | T | 1 | a0003c0003t0001g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.370-1338C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663758 | ||||||
| chr13:39663774
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-1322G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663774 | ||||||
| chr13:39663890
|
T | TA | 203 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.370-1190dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | |||||
| chr13:39663890
|
T | TAA | 8 | a0001c0001t0003g0014a0002c0002t0003g0224a0002c0002t0003g0228others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1191_370-1190d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | |||||
| chr13:39663890
|
TA | T | 6 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 6 | HG01256.hp2 HG02896.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1190delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | |||||
| chr13:39663972
|
A | G | 2 | a0002c0002t0003g0224a0002c0002t0004g0225 | 2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.370-1124A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663972 | ||||||
| chr13:39664025
|
C | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-1071C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664025 | ||||||
| chr13:39664038
|
C | T | 132 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0206others(129): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.370-1058C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664038 | ||||||
| chr13:39664119
|
G | T | 4 | a0002c0002t0002g0322a0002c0002t0002g0323a0002c0002t0002g0324others(1): Show | 4 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-977G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664119 | ||||||
| chr13:39664120
|
T | C | 2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.370-976T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664120 | ||||||
| chr13:39664250
|
T | C | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-846T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664250 | ||||||
| chr13:39664344
|
T | C | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-752T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664344 | ||||||
| chr13:39664346
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-750G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664346 | ||||||
| chr13:39664355
|
C | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-741C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664355 | ||||||
| chr13:39664356
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.370-740G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664356 | ||||||
| chr13:39664484
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-612T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664484 | ||||||
| chr13:39664512
|
C | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-584C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664512 | ||||||
| chr13:39664598
|
G | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-498G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664598 | ||||||
| chr13:39664704
|
A | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-392A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664704 | ||||||
| chr13:39664762
|
C | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-334C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664762 | ||||||
| chr13:39664866
|
A | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-230A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664866 | ||||||
| chr13:39664907
|
T | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-189T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664907 | ||||||
| chr13:39665002
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-94G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39665002 | ||||||
| chr13:39665328
|
G | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0200 | 3 | HG01496.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.428+174G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665328 | ||||||
| chr13:39665386
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.428+232T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665386 | ||||||
| chr13:39665481
|
A | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+327A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665481 | ||||||
| chr13:39665514
|
C | T | 8 | a0002c0002t0002g0245a0002c0002t0002g0316a0002c0002t0002g0317others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.428+360C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665514 | ||||||
| chr13:39665518
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.428+364T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665518 | ||||||
| chr13:39665584
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.428+430T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665584 | ||||||
| chr13:39665608
|
G | A | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.428+454G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665608 | ||||||
| chr13:39665627
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+473G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665627 | ||||||
| chr13:39665648
|
G | T | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+494G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665648 | ||||||
| chr13:39665721
|
T | C | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.428+567T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665721 | ||||||
| chr13:39665726
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.428+572G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665726 | ||||||
| chr13:39665797
|
C | T | 1 | a0002c0002t0002g0315 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.428+643C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665797 | ||||||
| chr13:39665896
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+742T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665896 | ||||||
| chr13:39665981
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.428+827T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665981 | ||||||
| chr13:39666023
|
C | T | 2 | a0002c0002t0002g0314a0002c0002t0003g0224 | 2 | HG02886.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.428+869C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666023 | ||||||
| chr13:39666244
|
T | C | 138 | a0001c0001t0003g0014a0001c0001t0004g0085a0001c0001t0004g0086others(135): Show | 140 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.428+1090T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666244 | ||||||
| chr13:39666298
|
G | A | 2 | a0002c0002t0003g0224a0002c0002t0004g0225 | 2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.428+1144G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666298 | ||||||
| chr13:39666343
|
G | A | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.428+1189G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666343 | ||||||
| chr13:39666367
|
C | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.428+1213C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666367 | ||||||
| chr13:39666543
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.428+1389A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666543 | ||||||
| chr13:39666551
|
G | A | 6 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(3): Show | 6 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+1397G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666551 | ||||||
| chr13:39666555
|
C | T | 1 | a0002c0002t0002g0313 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428+1401C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666555 | ||||||
| chr13:39666577
|
CACTGATC others(10): Show |
C | 77 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(74): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.428+1424_428+1440d others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666577 | ||||||
| chr13:39666597
|
T | C | 6 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0003t0001g0099others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+1443T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666597 | ||||||
| chr13:39666641
|
A | C | 17 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0027others(14): Show | 20 | HG00423.hp1 NA18946.hp2 NA18949.hp2 others(17): Show |
intron_variant | MODIFIER | c.428+1487A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666641 | ||||||
| chr13:39666739
|
A | G | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+1585A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666739 | ||||||
| chr13:39666789
|
T | C | 1 | a0002c0002t0002g0250 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.428+1635T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666789 | ||||||
| chr13:39667126
|
A | G | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+1972A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667126 | ||||||
| chr13:39667527
|
A | G | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.428+2373A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667527 | ||||||
| chr13:39667590
|
C | T | 7 | a0001c0001t0004g0206a0002c0002t0002g0308a0002c0002t0002g0309others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+2436C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667590 | ||||||
| chr13:39667622
|
A | T | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.428+2468A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667622 | ||||||
| chr13:39667736
|
G | T | 215 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(212): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.428+2582G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667736 | ||||||
| chr13:39667806
|
T | C | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.428+2652T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667806 | ||||||
| chr13:39667831
|
A | G | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.428+2677A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667831 | ||||||
| chr13:39667960
|
C | T | 215 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(212): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.428+2806C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667960 | ||||||
| chr13:39668018
|
T | A | 1 | a0001c0001t0004g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.428+2864T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668018 | ||||||
| chr13:39668051
|
G | A | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+2897G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668051 | ||||||
| chr13:39668056
|
A | G | 1 | a0002c0002t0002g0307 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.428+2902A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668056 | ||||||
| chr13:39668102
|
TACGATTC others(8): Show |
T | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+2951_428+2965d others(17): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39668102 | |||||
| chr13:39668200
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.428+3046C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668200 | ||||||
| chr13:39668206
|
A | G | 9 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0010others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+3052A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668206 | ||||||
| chr13:39668234
|
A | G | 225 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.428+3080A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668234 | ||||||
| chr13:39668416
|
T | C | 3 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0325 | 3 | NA18942.hp2 NA18955.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.428+3262T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668416 | ||||||
| chr13:39668511
|
G | A | 225 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.428+3357G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668511 | ||||||
| chr13:39668517
|
C | T | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+3363C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668517 | ||||||
| chr13:39668555
|
G | A | 4 | a0002c0002t0002g0336a0002c0002t0002g0337a0002c0002t0002g0338others(1): Show | 4 | HG03041.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+3401G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668555 | ||||||
| chr13:39668577
|
A | G | 225 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.428+3423A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668577 | ||||||
| chr13:39668584
|
C | T | 225 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.428+3430C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668584 | ||||||
| chr13:39668603
|
G | A | 2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.428+3449G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668603 | ||||||
| chr13:39668741
|
A | T | 225 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.428+3587A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668741 | ||||||
| chr13:39668777
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+3623G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668777 | ||||||
| chr13:39668778
|
A | C | 2 | a0001c0001t0004g0066a0001c0001t0004g0067 | 2 | NA18971.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.428+3624A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668778 | ||||||
| chr13:39668804
|
A | G | 13 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0003g0070others(10): Show | 15 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(12): Show |
intron_variant | MODIFIER | c.428+3650A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668804 | ||||||
| chr13:39668834
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.428+3680G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668834 | ||||||
| chr13:39668861
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.428+3707G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668861 | ||||||
| chr13:39668958
|
G | A | 7 | a0001c0001t0004g0206a0002c0002t0002g0308a0002c0002t0002g0309others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+3804G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668958 | ||||||
| chr13:39669006
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.428+3852C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669006 | ||||||
| chr13:39669025
|
TAC | T | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.428+3875_428+3876d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39669025 | |||||
| chr13:39669063
|
G | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | NA18747.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.428+3909G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669063 | ||||||
| chr13:39669068
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.428+3914A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669068 | ||||||
| chr13:39669117
|
C | T | 7 | a0001c0001t0004g0206a0002c0002t0002g0308a0002c0002t0002g0309others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+3963C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669117 | ||||||
| chr13:39669249
|
C | T | 74 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.428+4095C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669249 | ||||||
| chr13:39669283
|
T | C | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.428+4129T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669283 | ||||||
| chr13:39669331
|
T | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428+4177T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669331 | ||||||
| chr13:39669408
|
A | C | 2 | a0002c0002t0007g0306a0002c0002t0011g0012 | 3 | HG02572.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.428+4254A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669408 | ||||||
| chr13:39669463
|
C | T | 2 | a0003c0003t0001g0100a0003c0003t0001g0101 | 2 | HG01243.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.428+4309C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669463 | ||||||
| chr13:39669575
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0176 | 3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.428+4421A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669575 | ||||||
| chr13:39669668
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.428+4514T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669668 | ||||||
| chr13:39669691
|
G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.428+4537G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669691 | ||||||
| chr13:39669921
|
G | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+4767G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669921 | ||||||
| chr13:39670221
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.428+5067C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670221 | ||||||
| chr13:39670305
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.428+5151A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670305 | ||||||
| chr13:39670367
|
ATC | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+5217_428+5218d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39670367 | |||||
| chr13:39670449
|
T | C | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.428+5295T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670449 | ||||||
| chr13:39670604
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0185 | 3 | HG00280.hp1 HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.428+5450G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670604 | ||||||
| chr13:39670606
|
A | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0185 | 3 | HG00280.hp1 HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.428+5452A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670606 | ||||||
| chr13:39670617
|
G | C | 351 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.428+5463G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670617 | ||||||
| chr13:39670793
|
G | A | 9 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0010others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+5639G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670793 | ||||||
| chr13:39670968
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.428+5814C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670968 | ||||||
| chr13:39671020
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.428+5866A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671020 | ||||||
| chr13:39671040
|
T | C | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.428+5886T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671040 | ||||||
| chr13:39671150
|
A | T | 135 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0004g0085others(132): Show | 137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.428+5996A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671150 | ||||||
| chr13:39671363
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.429-6105G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671363 | ||||||
| chr13:39671365
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.429-6103G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671365 | ||||||
| chr13:39671388
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.429-6080C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671388 | ||||||
| chr13:39671547
|
T | C | 1 | a0002c0002t0002g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.429-5921T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671547 | ||||||
| chr13:39671566
|
A | C | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.429-5902A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671566 | ||||||
| chr13:39671570
|
T | G | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.429-5898T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671570 | ||||||
| chr13:39671649
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429-5819G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671649 | ||||||
| chr13:39671775
|
C | A | 1 | a0001c0001t0003g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.429-5693C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671775 | ||||||
| chr13:39671796
|
T | C | 10 | a0002c0002t0002g0322a0002c0002t0002g0323a0002c0002t0002g0324others(7): Show | 11 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-5672T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671796 | ||||||
| chr13:39671939
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429-5529A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671939 | ||||||
| chr13:39671977
|
G | C | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-5491G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671977 | ||||||
| chr13:39672030
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.429-5438A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672030 | ||||||
| chr13:39672220
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.429-5248T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672220 | ||||||
| chr13:39672225
|
A | G | 2 | a0002c0002t0007g0306a0002c0002t0011g0012 | 3 | HG02572.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.429-5243A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672225 | ||||||
| chr13:39672226
|
T | C | 1 | a0002c0002t0002g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.429-5242T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672226 | ||||||
| chr13:39672453
|
C | T | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-5015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672453 | ||||||
| chr13:39672538
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-4930C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672538 | ||||||
| chr13:39672549
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.429-4919A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672549 | ||||||
| chr13:39672650
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-4818A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672650 | ||||||
| chr13:39673033
|
TG | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.429-4433delG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39673033 | |||||
| chr13:39673109
|
G | C | 2 | a0002c0002t0004g0215a0002c0002t0004g0216 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.429-4359G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673109 | ||||||
| chr13:39673169
|
C | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0176 | 3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.429-4299C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673169 | ||||||
| chr13:39673237
|
G | A | 215 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(212): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.429-4231G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673237 | ||||||
| chr13:39673279
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.429-4189G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673279 | ||||||
| chr13:39673312
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-4156T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673312 | ||||||
| chr13:39673420
|
T | C | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.429-4048T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673420 | ||||||
| chr13:39673447
|
G | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-4021G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673447 | ||||||
| chr13:39673539
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.429-3929T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673539 | ||||||
| chr13:39673954
|
TTCTG | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-3510_429-3507d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39673954 | |||||
| chr13:39673978
|
A | G | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-3490A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673978 | ||||||
| chr13:39674008
|
T | C | 6 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0003t0001g0099others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-3460T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674008 | ||||||
| chr13:39674064
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-3404A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674064 | ||||||
| chr13:39674210
|
C | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-3258C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674210 | ||||||
| chr13:39674280
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.429-3188C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674280 | ||||||
| chr13:39674315
|
TCTTTA | T | 3 | a0001c0001t0004g0170a0001c0001t0004g0171a0001c0001t0004g0172 | 3 | HG02280.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.429-3148_429-3144d others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39674315 | |||||
| chr13:39674412
|
C | T | 351 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.429-3056C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674412 | ||||||
| chr13:39674507
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.429-2961C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674507 | ||||||
| chr13:39674508
|
G | A | 2 | a0002c0002t0004g0215a0002c0002t0004g0216 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.429-2960G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674508 | ||||||
| chr13:39674536
|
G | T | 2 | a0002c0002t0002g0305a0002c0002t0002g0344 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.429-2932G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674536 | ||||||
| chr13:39674597
|
A | G | 1 | a0002c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.429-2871A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674597 | ||||||
| chr13:39674635
|
A | T | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.429-2833A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674635 | ||||||
| chr13:39674640
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.429-2828A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674640 | ||||||
| chr13:39674665
|
T | G | 1 | a0004c0004t0007g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.429-2803T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674665 | ||||||
| chr13:39674852
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0005g0209 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.429-2616G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674852 | ||||||
| chr13:39674867
|
C | A | 9 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(6): Show | 9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-2601C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674867 | ||||||
| chr13:39674869
|
G | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-2599G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674869 | ||||||
| chr13:39674920
|
A | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-2548A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674920 | ||||||
| chr13:39675103
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0003g0008a0001c0001t0003g0189 | 4 | HG01243.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-2365A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675103 | ||||||
| chr13:39675198
|
T | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-2270T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675198 | ||||||
| chr13:39675421
|
C | G | 1 | a0002c0002t0002g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.429-2047C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675421 | ||||||
| chr13:39676023
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.429-1445T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676023 | ||||||
| chr13:39676111
|
T | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-1357T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676111 | ||||||
| chr13:39676268
|
C | T | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.429-1200C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676268 | ||||||
| chr13:39676487
|
CA | C | 4 | a0001c0001t0003g0014a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-980delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676487 | ||||||
| chr13:39676497
|
C | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0015g0202 | 3 | HG00140.hp2 HG00323.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.429-971C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676497 | ||||||
| chr13:39676550
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-918G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676550 | ||||||
| chr13:39676738
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.429-730A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676738 | ||||||
| chr13:39676953
|
G | A | 2 | a0001c0001t0003g0061a0001c0001t0003g0080 | 2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.429-515G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676953 | ||||||
| chr13:39677121
|
T | A | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.429-347T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677121 | ||||||
| chr13:39677142
|
A | G | 1 | a0006c0008t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.429-326A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677142 | ||||||
| chr13:39677188
|
T | G | 4 | a0001c0001t0003g0014a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-280T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677188 | ||||||
| chr13:39677285
|
A | G | 211 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(208): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.429-183A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677285 | ||||||
| chr13:39677658
|
A | T | 1 | a0002c0002t0002g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.540+79A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677658 | ||||||
| chr13:39677714
|
A | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 64 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+135A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677714 | ||||||
| chr13:39677874
|
T | C | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.540+295T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677874 | ||||||
| chr13:39677893
|
A | G | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.540+314A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677893 | ||||||
| chr13:39677902
|
T | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.540+323T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677902 | ||||||
| chr13:39677941
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.540+362C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677941 | ||||||
| chr13:39678046
|
A | T | 1 | a0001c0001t0004g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.540+467A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678046 | ||||||
| chr13:39678053
|
C | T | 125 | a0001c0001t0004g0085a0001c0001t0004g0086a0002c0002t0002g0011others(122): Show | 127 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.540+474C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678053 | ||||||
| chr13:39678463
|
C | T | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.540+884C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678463 | ||||||
| chr13:39678466
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+887G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678466 | ||||||
| chr13:39678587
|
A | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-951A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678587 | ||||||
| chr13:39678596
|
A | G | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.541-942A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678596 | ||||||
| chr13:39678723
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.541-815C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678723 | ||||||
| chr13:39678919
|
GTTA | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.541-601_541-599del others(3): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 39678919 | |||||
| chr13:39679082
|
A | G | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.541-456A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679082 | ||||||
| chr13:39679383
|
C | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0199 | 2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.541-155C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679383 | ||||||
| chr13:39679384
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0004g0091 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.541-154G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679384 | ||||||
| chr13:39679431
|
C | G | 1 | a0002c0002t0006g0302 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.541-107C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679431 | ||||||
| chr13:39679458
|
C | T | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.541-80C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679458 | ||||||
| chr13:39679764
|
A | G | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.623+144A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679764 | ||||||
| chr13:39679772
|
A | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.623+152A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679772 | ||||||
| chr13:39679805
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624-170T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679805 | ||||||
| chr13:39679963
|
A | AT | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
splice_acceptor_variant&intron_variant | HIGH | c.624-3dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 39679963 | |||||
| chr13:39680144
|
TCAAA | T | 74 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.694+102_694+105del others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 39680144 | |||||
| chr13:39680178
|
A | G | 1 | a0001c0001t0003g0063 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.694+133A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680178 | ||||||
| chr13:39680241
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694+196A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680241 | ||||||
| chr13:39680253
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+208C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680253 | ||||||
| chr13:39680388
|
T | C | 3 | a0001c0001t0003g0025a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG01433.hp2 HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.694+343T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680388 | ||||||
| chr13:39680410
|
T | C | 4 | a0001c0001t0003g0014a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+365T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680410 | ||||||
| chr13:39680454
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+409G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680454 | ||||||
| chr13:39680717
|
G | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.694+672G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680717 | ||||||
| chr13:39680880
|
T | A | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.694+835T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680880 | ||||||
| chr13:39680974
|
T | A | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.694+929T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680974 | ||||||
| chr13:39681126
|
A | G | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.695-1045A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681126 | ||||||
| chr13:39681150
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.695-1021T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681150 | ||||||
| chr13:39681223
|
C | T | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.695-948C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681223 | ||||||
| chr13:39681254
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.695-917A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681254 | ||||||
| chr13:39681454
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-717T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681454 | ||||||
| chr13:39681660
|
T | A | 6 | a0002c0002t0007g0306a0002c0002t0011g0012a0004c0004t0002g0254others(3): Show | 7 | HG02572.hp1 HG03041.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-511T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681660 | ||||||
| chr13:39681689
|
G | A | 1 | a0002c0002t0002g0309 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-482G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681689 | ||||||
| chr13:39681740
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.695-431A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681740 | ||||||
| chr13:39681996
|
C | G | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.695-175C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681996 | ||||||
| chr13:39682093
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.695-78T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682093 | ||||||
| chr13:39682115
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-56C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682115 | ||||||
| chr13:39682129
|
A | C | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-42A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682129 | ||||||
| chr13:39682346
|
G | A | 76 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(73): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.788+82G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682346 | ||||||
| chr13:39682389
|
A | G | 5 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0003t0001g0099others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+125A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682389 | ||||||
| chr13:39682407
|
A | C | 1 | a0002c0002t0002g0356 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.788+143A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682407 | ||||||
| chr13:39682450
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+186A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682450 | ||||||
| chr13:39682451
|
T | C | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.788+187T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682451 | ||||||
| chr13:39682484
|
C | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+220C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682484 | ||||||
| chr13:39682520
|
T | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.788+256T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682520 | ||||||
| chr13:39682590
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.788+326A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682590 | ||||||
| chr13:39682619
|
G | A | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.788+355G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682619 | ||||||
| chr13:39682905
|
G | C | 1 | a0002c0002t0002g0329 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788+641G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682905 | ||||||
| chr13:39682915
|
A | G | 1 | a0001c0001t0004g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.788+651A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682915 | ||||||
| chr13:39683004
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG00673.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.788+740A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683004 | ||||||
| chr13:39683283
|
G | A | 217 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.788+1019G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683283 | ||||||
| chr13:39683290
|
G | A | 4 | a0002c0002t0002g0322a0002c0002t0002g0323a0002c0002t0002g0324others(1): Show | 4 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+1026G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683290 | ||||||
| chr13:39683367
|
C | T | 25 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0095others(22): Show | 25 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.788+1103C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683367 | ||||||
| chr13:39683423
|
G | A | 3 | a0002c0002t0007g0306a0002c0002t0011g0012a0004c0004t0002g0254 | 4 | HG02572.hp1 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+1159G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683423 | ||||||
| chr13:39683425
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.788+1161A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683425 | ||||||
| chr13:39683434
|
A | G | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.788+1170A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683434 | ||||||
| chr13:39683437
|
T | C | 1 | a0001c0001t0005g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.788+1173T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683437 | ||||||
| chr13:39683708
|
CA | C | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+1445delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683708 | ||||||
| chr13:39683747
|
T | TA | 224 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(221): Show | 230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.788+1494dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39683747 | |||||
| chr13:39683783
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.788+1519T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683783 | ||||||
| chr13:39683812
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.788+1548T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683812 | ||||||
| chr13:39683830
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.788+1566G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683830 | ||||||
| chr13:39683918
|
G | T | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.788+1654G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683918 | ||||||
| chr13:39683948
|
G | A | 216 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(213): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.788+1684G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683948 | ||||||
| chr13:39683988
|
A | G | 1 | a0002c0002t0002g0301 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.788+1724A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683988 | ||||||
| chr13:39684117
|
C | T | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.788+1853C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684117 | ||||||
| chr13:39684186
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.788+1922G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684186 | ||||||
| chr13:39684243
|
A | AT | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 101 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.788+2004dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATT | 22 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0120others(19): Show | 23 | HG01175.hp2 HG01258.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.788+2003_788+2004d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTT | 8 | a0001c0001t0001g0093a0001c0001t0001g0121a0001c0001t0001g0152others(5): Show | 8 | HG01243.hp2 HG01934.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+2002_788+2004d others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(1): Show |
28 | a0001c0001t0004g0085a0001c0001t0004g0086a0002c0002t0002g0240others(25): Show | 28 | HG00609.hp2 HG01169.hp2 HG02698.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+1997_788+2004d others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(2): Show |
36 | a0002c0002t0002g0230a0002c0002t0002g0236a0002c0002t0002g0239others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.788+1996_788+2004d others(11): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(3): Show |
35 | a0001c0001t0003g0065a0001c0001t0004g0206a0002c0002t0002g0011others(32): Show | 36 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.788+1995_788+2004d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(4): Show |
38 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.788+1994_788+2004d others(13): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(5): Show |
29 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0026others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.788+1993_788+2004d others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(6): Show |
16 | a0001c0001t0003g0023a0001c0001t0003g0025a0001c0001t0003g0030others(13): Show | 16 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.788+1992_788+2004d others(15): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.788+1991_788+2004d others(16): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0056 | 2 | HG02040.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.788+1990_788+2004d others(17): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.788+1988_788+2004d others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(11): Show |
1 | a0002c0002t0002g0329 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788+1987_788+2004d others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(15): Show |
2 | a0002c0002t0002g0322a0002c0002t0002g0323 | 2 | HG01099.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.788+1983_788+2004d others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
A | ATTTTTTT others(16): Show |
1 | a0002c0002t0002g0324 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.788+1982_788+2004d others(25): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
ATTTTTT | A | 12 | a0001c0001t0003g0020a0002c0002t0002g0248a0002c0002t0002g0249others(9): Show | 12 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.788+1999_788+2004d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+1995_788+2004d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684243
|
ATTTTTTT others(4): Show |
A | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.788+1994_788+2004d others(13): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | |||||
| chr13:39684308
|
A | G | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.788+2044A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684308 | ||||||
| chr13:39684350
|
C | T | 1 | a0002c0002t0002g0314 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.788+2086C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684350 | ||||||
| chr13:39684530
|
G | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+2266G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684530 | ||||||
| chr13:39684815
|
C | T | 1 | a0002c0007t0002g0300 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.788+2551C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684815 | ||||||
| chr13:39685286
|
A | G | 4 | a0001c0001t0003g0014a0005c0005t0003g0015a0005c0005t0003g0016others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-2217A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685286 | ||||||
| chr13:39685353
|
C | A | 132 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0206others(129): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.789-2150C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685353 | ||||||
| chr13:39685419
|
A | G | 1 | a0002c0002t0007g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.789-2084A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685419 | ||||||
| chr13:39685488
|
C | T | 1 | a0004c0004t0002g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.789-2015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685488 | ||||||
| chr13:39685571
|
T | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.789-1932T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685571 | ||||||
| chr13:39685589
|
T | C | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.789-1914T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685589 | ||||||
| chr13:39685629
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.789-1874C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685629 | ||||||
| chr13:39685871
|
G | GTAC | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.789-1630_789-1629i others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39685871 | |||||
| chr13:39685913
|
A | G | 6 | a0002c0002t0002g0244a0002c0002t0002g0286a0002c0002t0002g0287others(3): Show | 6 | HG00438.hp1 HG01167.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.789-1590A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685913 | ||||||
| chr13:39685945
|
G | A | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.789-1558G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685945 | ||||||
| chr13:39685971
|
A | G | 9 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0010others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.789-1532A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685971 | ||||||
| chr13:39686006
|
A | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.789-1497A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686006 | ||||||
| chr13:39686114
|
T | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.789-1389T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686114 | ||||||
| chr13:39686207
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.789-1296G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686207 | ||||||
| chr13:39686488
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.789-1015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686488 | ||||||
| chr13:39686920
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-583G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686920 | ||||||
| chr13:39687083
|
C | T | 351 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.789-420C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687083 | ||||||
| chr13:39687139
|
G | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0071a0001c0001t0003g0072others(8): Show | 13 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(10): Show |
intron_variant | MODIFIER | c.789-364G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687139 | ||||||
| chr13:39687241
|
C | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-262C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687241 | ||||||
| chr13:39687347
|
T | C | 8 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(5): Show | 8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.789-156T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687347 | ||||||
| chr13:39687385
|
A | G | 227 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(224): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.789-118A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687385 | ||||||
| chr13:39687426
|
T | C | 1 | a0002c0002t0002g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.789-77T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687426 | ||||||
| chr13:39687446
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.789-57C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687446 | ||||||
| chr13:39687658
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.917+27A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 9/18 | chr13 | 39687658 | ||||||
| chr13:39687808
|
A | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1009+9A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39687808 | ||||||
| chr13:39688109
|
C | T | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1009+310C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688109 | ||||||
| chr13:39688134
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1009+335G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688134 | ||||||
| chr13:39688468
|
A | G | 1 | a0001c0001t0012g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1009+669A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688468 | ||||||
| chr13:39688567
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1009+768C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688567 | ||||||
| chr13:39688593
|
A | G | 1 | a0002c0002t0002g0249 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1009+794A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688593 | ||||||
| chr13:39688623
|
T | C | 221 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(218): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1009+824T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688623 | ||||||
| chr13:39688798
|
A | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1010-962A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688798 | ||||||
| chr13:39689102
|
A | G | 1 | a0002c0002t0008g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1010-658A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689102 | ||||||
| chr13:39689119
|
A | T | 1 | a0002c0002t0002g0296 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1010-641A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689119 | ||||||
| chr13:39689238
|
T | C | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1010-522T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689238 | ||||||
| chr13:39689347
|
T | C | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1010-413T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689347 | ||||||
| chr13:39689703
|
A | G | 1 | a0005c0005t0003g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1010-57A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689703 | ||||||
| chr13:39689842
|
T | C | 71 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(68): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+18T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689842 | ||||||
| chr13:39689848
|
T | C | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1074+24T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689848 | ||||||
| chr13:39689929
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1074+105T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689929 | ||||||
| chr13:39690099
|
AT | A | 221 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(218): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1074+276delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690099 | ||||||
| chr13:39690291
|
T | C | 1 | a0002c0002t0002g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1074+467T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690291 | ||||||
| chr13:39690365
|
T | C | 1 | a0002c0002t0002g0331 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074+541T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690365 | ||||||
| chr13:39690678
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+854T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690678 | ||||||
| chr13:39690796
|
A | G | 1 | a0001c0001t0003g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1074+972A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690796 | ||||||
| chr13:39690807
|
T | A | 231 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1074+983T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690807 | ||||||
| chr13:39691132
|
A | G | 1 | a0002c0002t0002g0346 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1074+1308A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691132 | ||||||
| chr13:39691212
|
T | C | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1074+1388T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691212 | ||||||
| chr13:39691502
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1074+1678A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691502 | ||||||
| chr13:39691769
|
T | C | 231 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1074+1945T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691769 | ||||||
| chr13:39691863
|
A | G | 1 | a0002c0002t0002g0296 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1074+2039A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691863 | ||||||
| chr13:39691927
|
T | A | 215 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(212): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1074+2103T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691927 | ||||||
| chr13:39691976
|
T | TAAAG | 231 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1074+2155_1074+215 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr13 | 39691976 | |||||
| chr13:39692070
|
G | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1074+2246G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692070 | ||||||
| chr13:39692353
|
G | T | 1 | a0002c0002t0002g0309 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1075-2281G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692353 | ||||||
| chr13:39692538
|
C | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-2096C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692538 | ||||||
| chr13:39692839
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1075-1795G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692839 | ||||||
| chr13:39693009
|
T | C | 44 | a0001c0001t0004g0085a0001c0001t0004g0086a0002c0002t0002g0246others(41): Show | 44 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1075-1625T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693009 | ||||||
| chr13:39693099
|
G | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1075-1535G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693099 | ||||||
| chr13:39693165
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1075-1469C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693165 | ||||||
| chr13:39693179
|
T | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-1455T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693179 | ||||||
| chr13:39693263
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 5 | HG01192.hp1 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-1371T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693263 | ||||||
| chr13:39693636
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1075-998A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693636 | ||||||
| chr13:39693653
|
A | T | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1075-981A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693653 | ||||||
| chr13:39693669
|
T | C | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1075-965T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693669 | ||||||
| chr13:39694085
|
A | G | 231 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1075-549A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694085 | ||||||
| chr13:39694142
|
A | G | 134 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(131): Show | 135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1075-492A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694142 | ||||||
| chr13:39694201
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-433C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694201 | ||||||
| chr13:39694215
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG00438.hp2 NA18959.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-419A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694215 | ||||||
| chr13:39694419
|
T | G | 13 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0003g0070others(10): Show | 15 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(12): Show |
intron_variant | MODIFIER | c.1075-215T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694419 | ||||||
| chr13:39694548
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1075-86T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694548 | ||||||
| chr13:39694586
|
A | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | NA18747.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1075-48A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694586 | ||||||
| chr13:39694793
|
A | G | 78 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(75): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1166+68A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694793 | ||||||
| chr13:39694954
|
C | T | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1166+229C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694954 | ||||||
| chr13:39694955
|
G | GCA | 155 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0001others(152): Show | 160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1166+264_1166+265d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
G | GCACA | 26 | a0001c0001t0001g0208a0001c0001t0003g0003a0001c0001t0003g0036others(23): Show | 27 | HG01884.hp2 HG01891.hp1 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.1166+262_1166+265d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
G | GCGCA | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1166+231_1166+232i others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
GCA | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 85 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1166+264_1166+265d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
GCACA | G | 17 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0001g0119others(14): Show | 17 | HG01081.hp1 HG01106.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.1166+262_1166+265d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
GCACACA | G | 14 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0138others(11): Show | 14 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1166+260_1166+265d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694955
|
GCACACAC others(3): Show |
G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1166+256_1166+265d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | |||||
| chr13:39694959
|
A | G | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+234A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694959 | ||||||
| chr13:39694961
|
A | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166+236A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694961 | ||||||
| chr13:39694963
|
A | G | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+238A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694963 | ||||||
| chr13:39694965
|
A | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166+240A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694965 | ||||||
| chr13:39694990
|
C | CACA | 3 | a0001c0001t0003g0037a0002c0002t0002g0234a0002c0002t0009g0276 | 3 | HG02083.hp1 HG02293.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1166+265_1166+266i others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694990 | ||||||
| chr13:39694992
|
C | A | 1 | a0003c0003t0001g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1166+267C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694992 | ||||||
| chr13:39695111
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1166+386G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695111 | ||||||
| chr13:39695146
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1166+421G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695146 | ||||||
| chr13:39695228
|
A | G | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0200 | 3 | HG01496.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1166+503A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695228 | ||||||
| chr13:39695287
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1166+562G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695287 | ||||||
| chr13:39695288
|
G | C | 1 | a0002c0002t0002g0262 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1166+563G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695288 | ||||||
| chr13:39695655
|
A | G | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1166+930A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695655 | ||||||
| chr13:39696090
|
G | GT | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0200others(2): Show | 6 | HG01496.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1166+1372dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39696090 | |||||
| chr13:39696151
|
A | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1166+1426A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696151 | ||||||
| chr13:39696171
|
A | ATTGT | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1166+1449_1166+145 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39696171 | |||||
| chr13:39696351
|
G | T | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+1626G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696351 | ||||||
| chr13:39696515
|
A | G | 13 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166+1790A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696515 | ||||||
| chr13:39696520
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1166+1795T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696520 | ||||||
| chr13:39696690
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1166+1965A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696690 | ||||||
| chr13:39696737
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1166+2012G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696737 | ||||||
| chr13:39696745
|
T | G | 1 | a0001c0001t0004g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1166+2020T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696745 | ||||||
| chr13:39696854
|
C | T | 4 | a0002c0002t0005g0217a0002c0002t0005g0218a0002c0002t0005g0219others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166+2129C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696854 | ||||||
| chr13:39697173
|
C | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0197 | 2 | HG00738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1167-2328C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697173 | ||||||
| chr13:39697246
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167-2255G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697246 | ||||||
| chr13:39697344
|
C | CAAAG | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-2154_1167-215 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39697344 | |||||
| chr13:39697388
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167-2113C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697388 | ||||||
| chr13:39697584
|
C | T | 1 | a0002c0002t0007g0330 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167-1917C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697584 | ||||||
| chr13:39697591
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-1910A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697591 | ||||||
| chr13:39697662
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-1839A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697662 | ||||||
| chr13:39697716
|
T | G | 2 | a0002c0002t0002g0230a0002c0002t0002g0232 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1167-1785T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697716 | ||||||
| chr13:39697782
|
G | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-1719G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697782 | ||||||
| chr13:39697946
|
C | T | 351 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1167-1555C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697946 | ||||||
| chr13:39698130
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-1371G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698130 | ||||||
| chr13:39698179
|
TA | T | 77 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(74): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1167-1311delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39698179 | |||||
| chr13:39698216
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167-1285C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698216 | ||||||
| chr13:39698439
|
T | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1167-1062T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698439 | ||||||
| chr13:39698515
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1167-986A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698515 | ||||||
| chr13:39698734
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167-767T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698734 | ||||||
| chr13:39698734
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1167-767T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698734 | ||||||
| chr13:39698775
|
T | C | 1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1167-726T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698775 | ||||||
| chr13:39698912
|
T | C | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1167-589T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698912 | ||||||
| chr13:39698928
|
G | C | 8 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(5): Show | 8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167-573G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698928 | ||||||
| chr13:39698971
|
A | G | 2 | a0002c0002t0003g0224a0002c0002t0004g0225 | 2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1167-530A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698971 | ||||||
| chr13:39699213
|
TA | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167-287delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39699213 | ||||||
| chr13:39699645
|
A | G | 1 | a0004c0004t0002g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1284+27A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699645 | ||||||
| chr13:39699917
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0065 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1284+299G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699917 | ||||||
| chr13:39699990
|
C | G | 1 | a0002c0002t0002g0307 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1284+372C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699990 | ||||||
| chr13:39700253
|
T | A | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1284+635T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700253 | ||||||
| chr13:39700261
|
T | A | 17 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 17 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1284+643T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700261 | ||||||
| chr13:39700354
|
G | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+736G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700354 | ||||||
| chr13:39700435
|
A | C | 3 | a0001c0001t0003g0061a0001c0001t0003g0063a0001c0001t0003g0080 | 3 | NA18974.hp2 NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1284+817A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700435 | ||||||
| chr13:39700569
|
T | C | 2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1284+951T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700569 | ||||||
| chr13:39700627
|
A | G | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+1009A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700627 | ||||||
| chr13:39700765
|
C | T | 56 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(53): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1284+1147C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700765 | ||||||
| chr13:39700777
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1284+1159G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700777 | ||||||
| chr13:39700815
|
C | T | 1 | a0005c0005t0003g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1284+1197C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700815 | ||||||
| chr13:39700872
|
A | G | 2 | a0002c0002t0002g0284a0002c0002t0002g0285 | 2 | NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1284+1254A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700872 | ||||||
| chr13:39700892
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+1274C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700892 | ||||||
| chr13:39701020
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1284+1402A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701020 | ||||||
| chr13:39701345
|
A | T | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284+1727A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701345 | ||||||
| chr13:39701514
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1284+1896G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701514 | ||||||
| chr13:39701605
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+1987C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701605 | ||||||
| chr13:39701838
|
C | T | 78 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(75): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+2220C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701838 | ||||||
| chr13:39701908
|
G | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0152others(1): Show | 4 | HG01934.hp2 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+2290G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701908 | ||||||
| chr13:39702121
|
C | T | 77 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(74): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1284+2503C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702121 | ||||||
| chr13:39702228
|
T | C | 24 | a0001c0001t0004g0085a0001c0001t0004g0086a0002c0002t0002g0246others(21): Show | 24 | HG00323.hp2 HG00558.hp2 HG02698.hp2 others(21): Show |
intron_variant | MODIFIER | c.1284+2610T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702228 | ||||||
| chr13:39702389
|
A | C | 134 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(131): Show | 135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1284+2771A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702389 | ||||||
| chr13:39702394
|
C | T | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+2776C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702394 | ||||||
| chr13:39702411
|
ATATTAAA others(13): Show |
A | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1284+2799_1284+281 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39702411 | |||||
| chr13:39702572
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+2954A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702572 | ||||||
| chr13:39702585
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1284+2967T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702585 | ||||||
| chr13:39702663
|
C | T | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1284+3045C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702663 | ||||||
| chr13:39702686
|
C | T | 4 | a0002c0002t0006g0321a0004c0004t0002g0254a0004c0004t0002g0255others(1): Show | 4 | HG02970.hp1 HG03225.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+3068C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702686 | ||||||
| chr13:39702687
|
G | A | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+3069G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702687 | ||||||
| chr13:39702789
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+3171A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702789 | ||||||
| chr13:39702907
|
C | T | 1 | a0002c0002t0008g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1284+3289C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702907 | ||||||
| chr13:39703021
|
C | T | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+3403C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703021 | ||||||
| chr13:39703233
|
A | C | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284+3615A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703233 | ||||||
| chr13:39703340
|
A | C | 78 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(75): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+3722A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703340 | ||||||
| chr13:39703779
|
C | G | 1 | a0004c0004t0002g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1284+4161C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703779 | ||||||
| chr13:39703801
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+4183G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703801 | ||||||
| chr13:39703899
|
A | T | 78 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(75): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+4281A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703899 | ||||||
| chr13:39703925
|
G | A | 4 | a0002c0002t0008g0241a0002c0002t0008g0242a0002c0002t0008g0243others(1): Show | 4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+4307G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703925 | ||||||
| chr13:39704219
|
C | G | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+4601C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704219 | ||||||
| chr13:39704276
|
G | A | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1284+4658G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704276 | ||||||
| chr13:39704629
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG00642.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1284+5011G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704629 | ||||||
| chr13:39704802
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+5184C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704802 | ||||||
| chr13:39704927
|
C | T | 354 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1284+5309C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704927 | ||||||
| chr13:39704952
|
A | G | 134 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(131): Show | 135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1284+5334A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704952 | ||||||
| chr13:39705078
|
T | C | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1284+5460T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705078 | ||||||
| chr13:39705195
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+5577A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705195 | ||||||
| chr13:39705231
|
A | G | 2 | a0001c0001t0003g0061a0001c0001t0003g0080 | 2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1284+5613A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705231 | ||||||
| chr13:39705312
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1284+5694C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705312 | ||||||
| chr13:39705484
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0050 | 2 | HG01934.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1284+5866T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705484 | ||||||
| chr13:39705507
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1284+5889G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705507 | ||||||
| chr13:39705823
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0003g0008a0001c0001t0003g0189 | 4 | HG01243.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6205C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705823 | ||||||
| chr13:39705826
|
A | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+6208A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705826 | ||||||
| chr13:39705972
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1284+6354A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705972 | ||||||
| chr13:39706199
|
T | TTATATAT others(45): Show |
2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+6611_1284+661 others(56): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706199 | |||||
| chr13:39706210
|
C | T | 1 | a0001c0001t0004g0066 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1284+6592C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706210 | ||||||
| chr13:39706213
|
C | T | 1 | a0002c0002t0002g0269 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1284+6595C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706213 | ||||||
| chr13:39706215
|
T | A | 1 | a0002c0002t0002g0269 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1284+6597T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706215 | ||||||
| chr13:39706215
|
T | TTA | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1284+6610_1284+661 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706215 | |||||
| chr13:39706215
|
T | TTATATAT others(37): Show |
4 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0077others(1): Show | 4 | NA18955.hp2 NA19010.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6611_1284+661 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706215 | |||||
| chr13:39706235
|
T | TTA | 8 | a0002c0002t0002g0317a0002c0002t0002g0336a0002c0002t0002g0337others(5): Show | 8 | HG02970.hp1 HG03130.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+6630_1284+663 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | |||||
| chr13:39706235
|
T | TTATA | 122 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(119): Show | 123 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284+6628_1284+663 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | |||||
| chr13:39706235
|
T | TTATATA | 10 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(7): Show | 10 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284+6626_1284+663 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | |||||
| chr13:39706237
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0003g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1284+6632_1284+664 others(22): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706237 | |||||
| chr13:39706255
|
T | TTA | 70 | a0001c0001t0001g0144a0001c0001t0003g0001a0001c0001t0003g0004others(67): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATA | 49 | a0001c0001t0001g0089a0001c0001t0001g0145a0001c0001t0001g0180others(46): Show | 52 | HG00423.hp2 HG00741.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.1284+6657_1284+666 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATA | 78 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0108others(75): Show | 79 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1284+6655_1284+666 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(1): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0087others(54): Show | 61 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1284+6653_1284+666 others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(3): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0125a0001c0001t0001g0128others(15): Show | 19 | HG01069.hp1 HG01106.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1284+6651_1284+666 others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(5): Show |
9 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0152others(6): Show | 9 | HG01934.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284+6649_1284+666 others(16): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(7): Show |
3 | a0002c0002t0007g0332a0003c0003t0001g0100a0003c0003t0001g0101 | 3 | HG01243.hp2 HG03209.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1284+6647_1284+666 others(18): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0004g0091a0003c0003t0001g0177 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1284+6645_1284+666 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1284+6641_1284+666 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(31): Show |
1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0005g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(39): Show |
2 | a0001c0001t0001g0103a0001c0001t0004g0124 | 2 | HG06807.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(41): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0113 | 2 | NA19064.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(52): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(54): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(37): Show |
5 | a0001c0001t0001g0115a0001c0001t0001g0159a0001c0001t0001g0201others(2): Show | 5 | HG00099.hp2 HG00609.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(39): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0096 | 2 | NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(51): Show |
1 | a0001c0001t0001g0114 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(62): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(35): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0117others(1): Show | 4 | NA18981.hp2 NA18984.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(46): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(37): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0173 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(39): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0155a0001c0001t0015g0202 | 3 | HG00323.hp1 HG01069.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(65): Show |
1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(76): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(40): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(31): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0121a0001c0001t0001g0163 | 3 | HG02300.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0162 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(35): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0120a0001c0001t0001g0157 | 3 | HG03669.hp1 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(46): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(37): Show |
1 | a0001c0001t0001g0156 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(31): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0181 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(36): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706255
|
TTA | T | 4 | a0001c0001t0003g0019a0001c0001t0003g0075a0001c0001t0003g0076others(1): Show | 4 | HG02896.hp2 NA19007.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | |||||
| chr13:39706261
|
A | ATATATAT others(15): Show |
2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(26): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706261 | |||||
| chr13:39706261
|
A | ATATATAT others(21): Show |
8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(32): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706261 | |||||
| chr13:39706290
|
T | G | 1 | a0002c0002t0002g0354 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1284+6672T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706290 | ||||||
| chr13:39706292
|
G | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1284+6674G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706292 | ||||||
| chr13:39706452
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1284+6834G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706452 | ||||||
| chr13:39706612
|
T | TA | 78 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(75): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+7001dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706612 | |||||
| chr13:39706673
|
T | A | 80 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(77): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1284+7055T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706673 | ||||||
| chr13:39706680
|
A | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1284+7062A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706680 | ||||||
| chr13:39706715
|
T | C | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7097T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706715 | ||||||
| chr13:39706753
|
G | T | 77 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(74): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1284+7135G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706753 | ||||||
| chr13:39706764
|
A | G | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+7146A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706764 | ||||||
| chr13:39706771
|
C | T | 79 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(76): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1284+7153C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706771 | ||||||
| chr13:39706798
|
C | A | 1 | a0001c0001t0003g0126 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1284+7180C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706798 | ||||||
| chr13:39706874
|
G | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG00280.hp1 HG01081.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284+7256G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706874 | ||||||
| chr13:39706917
|
C | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+7299C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706917 | ||||||
| chr13:39707082
|
A | T | 9 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG00738.hp2 HG02293.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284+7464A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707082 | ||||||
| chr13:39707132
|
CT | C | 6 | a0001c0001t0001g0131a0001c0001t0001g0139a0001c0001t0001g0201others(3): Show | 6 | NA18612.hp2 NA18946.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+7528delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39707132 | |||||
| chr13:39707228
|
A | G | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7610A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707228 | ||||||
| chr13:39707301
|
G | A | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7683G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707301 | ||||||
| chr13:39707373
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+7755C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707373 | ||||||
| chr13:39707379
|
A | G | 2 | a0001c0001t0004g0104a0001c0001t0004g0124 | 2 | HG00099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+7761A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707379 | ||||||
| chr13:39707389
|
A | C | 3 | a0002c0002t0002g0298a0002c0002t0002g0304a0002c0002t0002g0328 | 3 | HG01069.hp1 HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1284+7771A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707389 | ||||||
| chr13:39707601
|
T | C | 341 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1284+7983T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707601 | ||||||
| chr13:39708039
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284+8421C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708039 | ||||||
| chr13:39708054
|
C | G | 4 | a0002c0002t0002g0245a0002c0002t0002g0316a0002c0002t0002g0318others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+8436C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708054 | ||||||
| chr13:39708476
|
A | G | 9 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0010others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1284+8858A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708476 | ||||||
| chr13:39708664
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1284+9046G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708664 | ||||||
| chr13:39708921
|
G | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+9303G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708921 | ||||||
| chr13:39709169
|
C | T | 1 | a0002c0002t0002g0353 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1284+9551C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709169 | ||||||
| chr13:39709225
|
G | A | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1284+9607G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709225 | ||||||
| chr13:39709459
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-9777C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709459 | ||||||
| chr13:39709636
|
G | A | 1 | a0002c0002t0002g0356 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1285-9600G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709636 | ||||||
| chr13:39709814
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-9422C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709814 | ||||||
| chr13:39709868
|
A | G | 1 | a0004c0004t0002g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1285-9368A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709868 | ||||||
| chr13:39709933
|
T | C | 1 | a0002c0002t0002g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1285-9303T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709933 | ||||||
| chr13:39709965
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-9271C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709965 | ||||||
| chr13:39710078
|
C | G | 10 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(7): Show | 10 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-9158C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710078 | ||||||
| chr13:39710108
|
A | G | 1 | a0002c0002t0007g0355 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1285-9128A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710108 | ||||||
| chr13:39710209
|
G | T | 351 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1285-9027G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710209 | ||||||
| chr13:39710236
|
G | C | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-9000G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710236 | ||||||
| chr13:39710248
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-8988G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710248 | ||||||
| chr13:39710535
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1285-8701G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710535 | ||||||
| chr13:39710555
|
C | A | 1 | a0001c0001t0003g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1285-8681C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710555 | ||||||
| chr13:39710685
|
T | C | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-8551T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710685 | ||||||
| chr13:39710714
|
A | G | 1 | a0006c0008t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1285-8522A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710714 | ||||||
| chr13:39710783
|
A | G | 8 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(5): Show | 8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1285-8453A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710783 | ||||||
| chr13:39710840
|
T | TTTC | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-8394_1285-839 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39710840 | |||||
| chr13:39710844
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-8392C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710844 | ||||||
| chr13:39710844
|
CT | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1285-8381delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39710844 | |||||
| chr13:39710845
|
T | C | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-8391T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710845 | ||||||
| chr13:39710847
|
T | C | 3 | a0001c0001t0003g0019a0001c0001t0004g0122a0001c0001t0004g0123 | 3 | HG02630.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-8389T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710847 | ||||||
| chr13:39710890
|
T | A | 70 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(67): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1285-8346T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710890 | ||||||
| chr13:39710949
|
C | T | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1285-8287C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710949 | ||||||
| chr13:39711042
|
C | CT | 7 | a0001c0001t0003g0026a0001c0001t0003g0048a0001c0001t0003g0053others(4): Show | 7 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-8184dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39711042 | |||||
| chr13:39711222
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-8014G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711222 | ||||||
| chr13:39711301
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7935C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711301 | ||||||
| chr13:39711490
|
G | C | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1285-7746G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711490 | ||||||
| chr13:39711508
|
TTCTAAGA others(20): Show |
T | 217 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(214): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1285-7726_1285-770 others(31): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39711508 | |||||
| chr13:39711591
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-7645T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711591 | ||||||
| chr13:39711686
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7550A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711686 | ||||||
| chr13:39711834
|
T | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-7402T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711834 | ||||||
| chr13:39711844
|
A | C | 1 | a0001c0001t0003g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285-7392A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711844 | ||||||
| chr13:39711888
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1285-7348C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711888 | ||||||
| chr13:39711943
|
T | A | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-7293T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711943 | ||||||
| chr13:39711977
|
A | T | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-7259A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711977 | ||||||
| chr13:39712000
|
C | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7236C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712000 | ||||||
| chr13:39712056
|
C | T | 1 | a0001c0001t0014g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1285-7180C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712056 | ||||||
| chr13:39712091
|
C | T | 2 | a0002c0002t0002g0230a0002c0002t0002g0232 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1285-7145C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712091 | ||||||
| chr13:39712236
|
T | C | 1 | a0002c0002t0002g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1285-7000T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712236 | ||||||
| chr13:39712267
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-6969C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712267 | ||||||
| chr13:39712321
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-6915G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712321 | ||||||
| chr13:39712406
|
T | TAGTCCCT others(332): Show |
2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1285-6814_1285-681 others(343): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39712406 | |||||
| chr13:39712462
|
T | C | 1 | a0002c0002t0002g0356 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1285-6774T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712462 | ||||||
| chr13:39712476
|
A | G | 3 | a0001c0001t0003g0019a0001c0001t0004g0122a0001c0001t0004g0123 | 3 | HG02630.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-6760A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712476 | ||||||
| chr13:39712864
|
C | T | 2 | a0002c0002t0002g0294a0002c0002t0002g0295 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1285-6372C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712864 | ||||||
| chr13:39712865
|
G | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-6371G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712865 | ||||||
| chr13:39713220
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-6016T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713220 | ||||||
| chr13:39713263
|
T | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-5973T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713263 | ||||||
| chr13:39713382
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1285-5854T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713382 | ||||||
| chr13:39713399
|
A | G | 1 | a0002c0002t0002g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1285-5837A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713399 | ||||||
| chr13:39713633
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-5603G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713633 | ||||||
| chr13:39713637
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-5599A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713637 | ||||||
| chr13:39713651
|
G | T | 1 | a0002c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1285-5585G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713651 | ||||||
| chr13:39713678
|
G | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-5558G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713678 | ||||||
| chr13:39713707
|
G | A | 137 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(134): Show | 138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1285-5529G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713707 | ||||||
| chr13:39713898
|
A | G | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-5338A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713898 | ||||||
| chr13:39713988
|
T | A | 1 | a0002c0002t0002g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1285-5248T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713988 | ||||||
| chr13:39714224
|
G | GT | 222 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(219): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1285-5001dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39714224 | |||||
| chr13:39714224
|
GT | G | 37 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(34): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1285-5001delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39714224 | |||||
| chr13:39714394
|
T | C | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1285-4842T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714394 | ||||||
| chr13:39714434
|
A | C | 1 | a0002c0002t0002g0234 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1285-4802A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714434 | ||||||
| chr13:39714549
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1285-4687G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714549 | ||||||
| chr13:39714622
|
C | A | 11 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(8): Show | 11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-4614C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714622 | ||||||
| chr13:39714784
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-4452A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714784 | ||||||
| chr13:39714786
|
T | A | 231 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1285-4450T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714786 | ||||||
| chr13:39714897
|
A | C | 1 | a0002c0002t0002g0295 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1285-4339A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714897 | ||||||
| chr13:39714933
|
T | G | 130 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(127): Show | 131 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1285-4303T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714933 | ||||||
| chr13:39714981
|
A | T | 138 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(135): Show | 139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1285-4255A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714981 | ||||||
| chr13:39715198
|
G | A | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-4038G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715198 | ||||||
| chr13:39715208
|
A | C | 1 | a0002c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1285-4028A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715208 | ||||||
| chr13:39715216
|
A | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-4020A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715216 | ||||||
| chr13:39715256
|
C | CCTCT | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1285-3967_1285-396 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715256 | |||||
| chr13:39715271
|
C | CTCTCTA | 171 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(168): Show | 172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1285-3964_1285-396 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715271 | |||||
| chr13:39715271
|
C | CTCTG | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-3964_1285-396 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715271 | |||||
| chr13:39715271
|
C | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-3965C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715271 | ||||||
| chr13:39715273
|
A | C | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3963A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715273 | ||||||
| chr13:39715274
|
T | C | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1285-3962T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715274 | ||||||
| chr13:39715283
|
A | C | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3953A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715283 | ||||||
| chr13:39715284
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3952C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715284 | ||||||
| chr13:39715286
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3950C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715286 | ||||||
| chr13:39715310
|
A | G | 1 | a0001c0001t0003g0039 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1285-3926A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715310 | ||||||
| chr13:39715386
|
C | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3850C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715386 | ||||||
| chr13:39715386
|
C | T | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1285-3850C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715386 | ||||||
| chr13:39715587
|
G | T | 1 | a0002c0002t0004g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1285-3649G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715587 | ||||||
| chr13:39715591
|
C | A | 1 | a0001c0001t0003g0032 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1285-3645C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715591 | ||||||
| chr13:39715904
|
T | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-3332T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715904 | ||||||
| chr13:39716052
|
A | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1285-3184A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716052 | ||||||
| chr13:39716059
|
G | A | 1 | a0004c0004t0007g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1285-3177G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716059 | ||||||
| chr13:39716196
|
T | A | 1 | a0002c0002t0004g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1285-3040T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716196 | ||||||
| chr13:39716342
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1285-2894C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716342 | ||||||
| chr13:39716359
|
C | G | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1285-2877C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716359 | ||||||
| chr13:39716390
|
A | T | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-2846A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716390 | ||||||
| chr13:39716560
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-2676G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716560 | ||||||
| chr13:39716582
|
C | G | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0200others(2): Show | 6 | HG01496.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1285-2654C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716582 | ||||||
| chr13:39716936
|
T | A | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-2300T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716936 | ||||||
| chr13:39717008
|
G | T | 133 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0170others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-2228G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717008 | ||||||
| chr13:39717149
|
G | A | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1285-2087G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717149 | ||||||
| chr13:39717266
|
A | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-1970A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717266 | ||||||
| chr13:39717282
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1954G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717282 | ||||||
| chr13:39717488
|
C | CA | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1285-1746dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39717488 | |||||
| chr13:39717548
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1688G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717548 | ||||||
| chr13:39717760
|
A | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1476A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717760 | ||||||
| chr13:39717812
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1285-1424G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717812 | ||||||
| chr13:39717869
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-1367A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717869 | ||||||
| chr13:39717883
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1285-1353A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717883 | ||||||
| chr13:39717980
|
T | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1256T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717980 | ||||||
| chr13:39717997
|
GT | G | 4 | a0002c0002t0008g0241a0002c0002t0008g0242a0002c0002t0008g0243others(1): Show | 4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-1235delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39717997 | |||||
| chr13:39718180
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0158 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1285-1056A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718180 | ||||||
| chr13:39718257
|
C | T | 1 | a0002c0002t0002g0314 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1285-979C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718257 | ||||||
| chr13:39718261
|
T | C | 1 | a0002c0002t0002g0317 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1285-975T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718261 | ||||||
| chr13:39718360
|
A | G | 4 | a0002c0002t0002g0239a0002c0002t0002g0240a0002c0002t0002g0293others(1): Show | 4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-876A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718360 | ||||||
| chr13:39718372
|
G | A | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1285-864G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718372 | ||||||
| chr13:39718399
|
G | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-837G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718399 | ||||||
| chr13:39718511
|
T | C | 2 | a0002c0002t0004g0215a0002c0002t0004g0216 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1285-725T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718511 | ||||||
| chr13:39718790
|
A | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1285-446A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718790 | ||||||
| chr13:39718804
|
C | T | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-432C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718804 | ||||||
| chr13:39718841
|
G | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1285-395G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718841 | ||||||
| chr13:39718847
|
G | A | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1285-389G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718847 | ||||||
| chr13:39718850
|
G | A | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1285-386G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718850 | ||||||
| chr13:39718925
|
A | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1285-311A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718925 | ||||||
| chr13:39719006
|
G | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01106.hp1 HG02074.hp2 NA19056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-230G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719006 | ||||||
| chr13:39719065
|
C | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-171C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719065 | ||||||
| chr13:39719085
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1285-151G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719085 | ||||||
| chr13:39719151
|
AT | A | 347 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(344): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1285-76delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39719151 | |||||
| chr13:39719178
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1285-58A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719178 | ||||||
| chr13:39719428
|
AATTCTGG others(13): Show |
A | 8 | a0002c0002t0002g0245a0002c0002t0002g0316a0002c0002t0002g0317others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416+64_1416+83del others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 39719428 | |||||
| chr13:39719464
|
CTCTT | C | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+102_1416+105d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 39719464 | |||||
| chr13:39719549
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 63 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1417-111C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | chr13 | 39719549 | ||||||
| chr13:39719994
|
A | AAC | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1584+199_1584+200d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | |||||
| chr13:39719994
|
A | AACAC | 122 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(119): Show | 123 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.1584+197_1584+200d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | |||||
| chr13:39719994
|
A | AACACAC | 28 | a0001c0001t0004g0206a0002c0002t0002g0237a0002c0002t0002g0239others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1584+195_1584+200d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | |||||
| chr13:39719994
|
AAC | A | 15 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1584+199_1584+200d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | |||||
| chr13:39719994
|
AACACAC | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1584+195_1584+200d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | |||||
| chr13:39720297
|
C | T | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1584+470C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720297 | ||||||
| chr13:39720402
|
G | A | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1584+575G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720402 | ||||||
| chr13:39720418
|
A | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+591A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720418 | ||||||
| chr13:39720613
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1584+786C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720613 | ||||||
| chr13:39720657
|
C | T | 1 | a0002c0002t0002g0342 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1584+830C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720657 | ||||||
| chr13:39720732
|
A | G | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+905A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720732 | ||||||
| chr13:39720830
|
A | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+1003A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720830 | ||||||
| chr13:39720931
|
T | C | 138 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(135): Show | 139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1584+1104T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720931 | ||||||
| chr13:39720992
|
A | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(53): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1584+1165A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720992 | ||||||
| chr13:39721126
|
C | G | 1 | a0002c0002t0002g0317 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1584+1299C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721126 | ||||||
| chr13:39721143
|
T | C | 1 | a0002c0002t0002g0344 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1584+1316T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721143 | ||||||
| chr13:39721243
|
G | A | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1584+1416G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721243 | ||||||
| chr13:39721303
|
A | G | 3 | a0002c0002t0002g0235a0002c0002t0006g0231a0002c0002t0006g0233 | 3 | HG01261.hp2 HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1584+1476A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721303 | ||||||
| chr13:39721351
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1584+1524A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721351 | ||||||
| chr13:39721422
|
T | C | 1 | a0002c0002t0002g0286 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1584+1595T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721422 | ||||||
| chr13:39721452
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1584+1625C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721452 | ||||||
| chr13:39721474
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1584+1647A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721474 | ||||||
| chr13:39721502
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1584+1675T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721502 | ||||||
| chr13:39721540
|
C | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+1713C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721540 | ||||||
| chr13:39721646
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585-1687A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721646 | ||||||
| chr13:39721879
|
A | T | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1454A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721879 | ||||||
| chr13:39721887
|
T | G | 2 | a0002c0002t0002g0342a0002c0002t0002g0343 | 2 | NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1585-1446T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721887 | ||||||
| chr13:39721950
|
T | C | 1 | a0001c0001t0013g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1585-1383T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721950 | ||||||
| chr13:39722084
|
G | A | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1249G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722084 | ||||||
| chr13:39722092
|
A | G | 1 | a0002c0002t0002g0288 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1585-1241A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722092 | ||||||
| chr13:39722177
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585-1156C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722177 | ||||||
| chr13:39722178
|
C | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1585-1155C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722178 | ||||||
| chr13:39722194
|
T | C | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585-1139T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722194 | ||||||
| chr13:39722229
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1585-1104C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722229 | ||||||
| chr13:39722236
|
G | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1585-1097G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722236 | ||||||
| chr13:39722310
|
TA | T | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG00642.hp2 HG00738.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.1585-1009delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722310 | |||||
| chr13:39722331
|
T | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1002T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722331 | ||||||
| chr13:39722395
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1585-938G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722395 | ||||||
| chr13:39722452
|
C | T | 1 | a0002c0002t0002g0314 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1585-881C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722452 | ||||||
| chr13:39722617
|
C | CA | 21 | a0001c0001t0001g0105a0001c0001t0001g0120a0001c0001t0003g0028others(18): Show | 21 | HG01081.hp2 HG01884.hp1 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.1585-699dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722617 | |||||
| chr13:39722617
|
CA | C | 121 | a0001c0001t0001g0131a0001c0001t0004g0085a0001c0001t0004g0086others(118): Show | 122 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1585-699delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722617 | |||||
| chr13:39722632
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1585-701A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722632 | ||||||
| chr13:39722704
|
C | A | 9 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0010others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-629C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722704 | ||||||
| chr13:39722711
|
C | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585-622C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722711 | ||||||
| chr13:39722804
|
A | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1585-529A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722804 | ||||||
| chr13:39722824
|
A | G | 3 | a0001c0001t0001g0180a0002c0002t0002g0239a0002c0002t0002g0240 | 3 | HG01168.hp1 HG01169.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1585-509A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722824 | ||||||
| chr13:39722839
|
C | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1585-494C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722839 | ||||||
| chr13:39722846
|
A | G | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1585-487A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722846 | ||||||
| chr13:39722892
|
C | T | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1585-441C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722892 | ||||||
| chr13:39722895
|
T | A | 133 | a0001c0001t0003g0064a0001c0001t0003g0199a0001c0001t0004g0085others(130): Show | 134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1585-438T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722895 | ||||||
| chr13:39722917
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1585-416C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722917 | ||||||
| chr13:39722918
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1585-415T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722918 | ||||||
| chr13:39722966
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1585-367G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722966 | ||||||
| chr13:39722971
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1585-362G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722971 | ||||||
| chr13:39723080
|
G | C | 2 | a0002c0002t0003g0228a0002c0002t0003g0229 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-253G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723080 | ||||||
| chr13:39723084
|
C | T | 1 | a0002c0002t0002g0341 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1585-249C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723084 | ||||||
| chr13:39723176
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1585-157C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723176 | ||||||
| chr13:39723230
|
A | G | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0084 | 3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1585-103A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723230 | ||||||
| chr13:39723244
|
C | T | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1585-89C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723244 | ||||||
| chr13:39723477
|
A | G | 9 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0200others(6): Show | 10 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1692+37A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723477 | ||||||
| chr13:39723501
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1692+61A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723501 | ||||||
| chr13:39723547
|
C | T | 234 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0089others(231): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1692+107C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723547 | ||||||
| chr13:39723619
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0186 | 2 | HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1692+179G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723619 | ||||||
| chr13:39723660
|
T | C | 66 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0138others(63): Show | 69 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1692+220T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723660 | ||||||
| chr13:39723696
|
G | T | 1 | a0002c0002t0002g0338 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1692+256G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723696 | ||||||
| chr13:39723702
|
A | G | 10 | a0001c0001t0005g0204a0001c0001t0005g0205a0002c0002t0002g0317others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1692+262A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723702 | ||||||
| chr13:39723724
|
GT | G | 3 | a0001c0001t0001g0089a0002c0002t0010g0223a0007c0009t0010g0222 | 3 | HG03471.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1692+289delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39723724 | |||||
| chr13:39723942
|
A | G | 1 | a0002c0002t0002g0259 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1692+502A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723942 | ||||||
| chr13:39723948
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1692+508A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723948 | ||||||
| chr13:39724039
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1693-469A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724039 | ||||||
| chr13:39724084
|
C | G | 1 | a0003c0003t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1693-424C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724084 | ||||||
| chr13:39724087
|
T | C | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693-421T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724087 | ||||||
| chr13:39724325
|
A | G | 1 | a0002c0002t0002g0299 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1693-183A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724325 | ||||||
| chr13:39724410
|
G | A | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1693-98G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724410 | ||||||
| chr13:39724451
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1693-57A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724451 | ||||||
| chr13:39724483
|
CT | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
splice_region_variant&intron_variant | LOW | c.1693-7delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39724483 | |||||
| chr13:39724484
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1693-24T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724484 | ||||||
| chr13:39724485
|
T | C | 88 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(85): Show | 95 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1693-23T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724485 | ||||||
| chr13:39724486
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0053 | 2 | HG01256.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1693-22T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724486 | ||||||
| chr13:39724501
|
TA | T | 137 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
splice_region_variant&intron_variant | LOW | c.1693-4delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39724501 | |||||
| chr13:39724502
|
A | T | 1 | a0002c0002t0002g0236 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.1693-6A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724502 | ||||||
| chr13:39724668
|
C | T | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1746+107C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39724668 | ||||||
| chr13:39724810
|
C | G | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1746+249C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39724810 | ||||||
| chr13:39725062
|
C | T | 5 | a0001c0001t0004g0102a0002c0002t0002g0352a0002c0002t0002g0353others(2): Show | 5 | HG00642.hp1 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746+501C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725062 | ||||||
| chr13:39725115
|
T | C | 142 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1746+554T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725115 | ||||||
| chr13:39725132
|
T | C | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1746+571T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725132 | ||||||
| chr13:39725292
|
CTT | C | 4 | a0001c0001t0003g0008a0001c0001t0003g0189a0002c0002t0003g0227others(1): Show | 5 | HG01243.hp1 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746+733_1746+734d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725292 | |||||
| chr13:39725585
|
A | C | 70 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(67): Show | 74 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1746+1024A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725585 | ||||||
| chr13:39725633
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1746+1072A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725633 | ||||||
| chr13:39725686
|
CTA | C | 139 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1746+1131_1746+113 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725686 | |||||
| chr13:39725705
|
ATAG | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1746+1148_1746+115 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725705 | |||||
| chr13:39725743
|
T | C | 6 | a0003c0003t0001g0097a0003c0003t0001g0098a0003c0003t0001g0099others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1746+1182T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725743 | ||||||
| chr13:39725815
|
A | G | 1 | a0003c0003t0001g0177 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1746+1254A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725815 | ||||||
| chr13:39726012
|
T | G | 2 | a0001c0001t0004g0196a0002c0002t0002g0238 | 2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1746+1451T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726012 | ||||||
| chr13:39726159
|
G | A | 1 | a0002c0002t0002g0339 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1747-1310G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726159 | ||||||
| chr13:39726191
|
T | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1747-1278T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726191 | ||||||
| chr13:39726408
|
A | G | 176 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1747-1061A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726408 | ||||||
| chr13:39726413
|
G | A | 2 | a0002c0002t0002g0294a0002c0002t0002g0295 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1747-1056G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726413 | ||||||
| chr13:39726437
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1747-1032A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726437 | ||||||
| chr13:39726548
|
G | A | 6 | a0002c0002t0002g0248a0002c0002t0002g0249a0002c0002t0002g0250others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-921G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726548 | ||||||
| chr13:39726615
|
C | G | 1 | a0002c0002t0003g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747-854C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726615 | ||||||
| chr13:39726710
|
G | C | 1 | a0004c0004t0002g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1747-759G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726710 | ||||||
| chr13:39726763
|
C | A | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0084 | 3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1747-706C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726763 | ||||||
| chr13:39726866
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1747-603G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726866 | ||||||
| chr13:39727166
|
C | A | 9 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747-303C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39727166 | ||||||
| chr13:39727319
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1747-150T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39727319 | ||||||
| chr13:39727319
|
T | TAGAAAAT others(161): Show |
1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1747-133_1747-132i others(170): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39727319 | |||||
| chr13:39727572
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1826+24G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727572 | ||||||
| chr13:39727626
|
T | A | 92 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(89): Show | 99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+78T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727626 | ||||||
| chr13:39727765
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1826+217G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727765 | ||||||
| chr13:39728212
|
G | A | 1 | a0002c0002t0002g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1826+664G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728212 | ||||||
| chr13:39728224
|
C | T | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1826+676C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728224 | ||||||
| chr13:39728260
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826+712A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728260 | ||||||
| chr13:39728273
|
A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 86 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.1826+725A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728273 | ||||||
| chr13:39728471
|
CT | C | 133 | a0001c0001t0004g0049a0001c0001t0004g0066a0001c0001t0004g0067others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1826+936delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39728471 | |||||
| chr13:39728553
|
TG | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+1006delG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728553 | ||||||
| chr13:39728674
|
T | G | 92 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(89): Show | 99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+1126T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728674 | ||||||
| chr13:39728708
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1826+1160C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728708 | ||||||
| chr13:39728716
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1826+1168C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728716 | ||||||
| chr13:39728807
|
G | A | 7 | a0001c0001t0003g0028a0001c0001t0003g0031a0001c0001t0003g0064others(4): Show | 7 | HG02004.hp2 HG02735.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+1259G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728807 | ||||||
| chr13:39728926
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1826+1378G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728926 | ||||||
| chr13:39728989
|
T | G | 1 | a0001c0001t0003g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1826+1441T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728989 | ||||||
| chr13:39729023
|
T | C | 141 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1826+1475T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729023 | ||||||
| chr13:39729057
|
C | T | 134 | a0001c0001t0004g0049a0001c0001t0004g0066a0001c0001t0004g0067others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1826+1509C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729057 | ||||||
| chr13:39729069
|
A | G | 1 | a0002c0002t0002g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1826+1521A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729069 | ||||||
| chr13:39729141
|
C | T | 1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1826+1593C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729141 | ||||||
| chr13:39729256
|
A | G | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1826+1708A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729256 | ||||||
| chr13:39729396
|
G | A | 1 | a0004c0004t0002g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1826+1848G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729396 | ||||||
| chr13:39729527
|
A | C | 1 | a0001c0001t0003g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1826+1979A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729527 | ||||||
| chr13:39729576
|
A | T | 91 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(88): Show | 98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+2028A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729576 | ||||||
| chr13:39729636
|
A | G | 88 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(85): Show | 94 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1826+2088A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729636 | ||||||
| chr13:39729666
|
A | G | 88 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(85): Show | 94 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1826+2118A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729666 | ||||||
| chr13:39729668
|
G | A | 1 | a0001c0001t0003g0038 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1826+2120G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729668 | ||||||
| chr13:39729768
|
G | A | 1 | a0002c0002t0010g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1826+2220G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729768 | ||||||
| chr13:39729890
|
A | G | 1 | a0002c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1826+2342A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729890 | ||||||
| chr13:39730103
|
C | A | 1 | a0002c0002t0002g0279 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1826+2555C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730103 | ||||||
| chr13:39730492
|
C | T | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826+2944C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730492 | ||||||
| chr13:39730558
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 6 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+3010G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730558 | ||||||
| chr13:39730654
|
T | G | 175 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+3106T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730654 | ||||||
| chr13:39730750
|
G | C | 1 | a0002c0002t0002g0298 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1826+3202G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730750 | ||||||
| chr13:39730757
|
G | A | 1 | a0002c0002t0002g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826+3209G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730757 | ||||||
| chr13:39730760
|
C | A | 1 | a0004c0004t0002g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826+3212C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730760 | ||||||
| chr13:39730773
|
C | CA | 7 | a0001c0001t0001g0178a0003c0003t0001g0097a0003c0003t0001g0098others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826+3251dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAA | 13 | a0001c0001t0001g0184a0001c0001t0003g0022a0001c0001t0003g0032others(10): Show | 15 | HG00639.hp2 HG01256.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826+3250_1826+325 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAA | 61 | a0001c0001t0001g0168a0001c0001t0003g0001a0001c0001t0003g0003others(58): Show | 65 | HG00140.hp1 HG00280.hp2 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.1826+3249_1826+325 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAA | 15 | a0001c0001t0003g0004a0001c0001t0003g0024a0001c0001t0003g0028others(12): Show | 16 | HG00741.hp2 HG01934.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.1826+3248_1826+325 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG00642.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1826+3241_1826+325 others(15): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1826+3238_1826+325 others(18): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(8): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 16 | HG00738.hp2 HG02040.hp2 HG03239.hp2 others(13): Show |
intron_variant | MODIFIER | c.1826+3237_1826+325 others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(9): Show |
19 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0125others(16): Show | 19 | HG01106.hp1 HG01516.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1826+3236_1826+325 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(10): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0092a0001c0001t0001g0107others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826+3235_1826+325 others(21): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(11): Show |
11 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0105others(8): Show | 11 | HG01169.hp1 HG01258.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826+3234_1826+325 others(22): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(4): Show | 7 | HG01081.hp1 HG01361.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+3233_1826+325 others(23): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(13): Show |
9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0103others(6): Show | 9 | HG00621.hp2 HG03239.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.1826+3232_1826+325 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0179 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1826+3231_1826+325 others(25): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1826+3229_1826+325 others(27): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0115 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1826+3227_1826+325 others(29): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1826+3251_1826+325 others(31): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0014g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1826+3251_1826+325 others(40): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
CA | C | 121 | a0001c0001t0001g0090a0001c0001t0001g0118a0001c0001t0001g0119others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1826+3251delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
CAA | C | 8 | a0002c0002t0002g0245a0002c0002t0002g0273a0002c0002t0002g0316others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826+3250_1826+325 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730773
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0157a0001c0001t0001g0159a0002c0002t0006g0320others(1): Show | 4 | HG02056.hp2 HG02970.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+3242_1826+325 others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | |||||
| chr13:39730790
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1826+3251_1826+325 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730790 | |||||
| chr13:39730790
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG00438.hp2 NA18967.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826+3251_1826+325 others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730790 | |||||
| chr13:39730800
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0176 | 3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1826+3252G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730800 | ||||||
| chr13:39730861
|
A | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+3313A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730861 | ||||||
| chr13:39730866
|
G | A | 2 | a0002c0002t0006g0320a0002c0002t0006g0321 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1826+3318G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730866 | ||||||
| chr13:39730911
|
T | A | 3 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0079 | 3 | NA19007.hp1 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1826+3363T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730911 | ||||||
| chr13:39730929
|
C | T | 1 | a0002c0002t0002g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1826+3381C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730929 | ||||||
| chr13:39730979
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+3431T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730979 | ||||||
| chr13:39731059
|
A | G | 1 | a0001c0001t0004g0049 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1826+3511A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731059 | ||||||
| chr13:39731087
|
T | C | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+3539T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731087 | ||||||
| chr13:39731320
|
T | C | 2 | a0002c0002t0004g0215a0002c0002t0004g0216 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1826+3772T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731320 | ||||||
| chr13:39731381
|
A | G | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1826+3833A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731381 | ||||||
| chr13:39731454
|
C | A | 91 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(88): Show | 98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+3906C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731454 | ||||||
| chr13:39731469
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1826+3921T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731469 | ||||||
| chr13:39731995
|
G | C | 1 | a0002c0002t0002g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1826+4447G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731995 | ||||||
| chr13:39732078
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1826+4530A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732078 | ||||||
| chr13:39732119
|
A | G | 175 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+4571A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732119 | ||||||
| chr13:39732551
|
T | G | 346 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(343): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1826+5003T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732551 | ||||||
| chr13:39732982
|
T | C | 175 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+5434T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732982 | ||||||
| chr13:39733123
|
C | T | 91 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(88): Show | 98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+5575C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733123 | ||||||
| chr13:39733189
|
C | CT | 7 | a0001c0001t0001g0148a0001c0001t0001g0151a0001c0001t0001g0157others(4): Show | 7 | HG03927.hp1 HG04115.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+5659dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39733189 | |||||
| chr13:39733213
|
C | T | 1 | a0002c0002t0003g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1826+5665C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733213 | ||||||
| chr13:39733227
|
G | T | 8 | a0002c0002t0002g0270a0002c0002t0002g0271a0002c0002t0002g0272others(5): Show | 8 | HG00609.hp2 HG02027.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826+5679G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733227 | ||||||
| chr13:39733288
|
G | T | 172 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1826+5740G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733288 | ||||||
| chr13:39733308
|
G | A | 1 | a0001c0001t0013g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1826+5760G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733308 | ||||||
| chr13:39733380
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1826+5832G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733380 | ||||||
| chr13:39733400
|
C | T | 138 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1826+5852C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733400 | ||||||
| chr13:39733419
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1826+5871G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733419 | ||||||
| chr13:39733459
|
G | A | 1 | a0002c0002t0002g0340 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1826+5911G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733459 | ||||||
| chr13:39733476
|
A | C | 1 | a0001c0001t0003g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1826+5928A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733476 | ||||||
| chr13:39733477
|
C | A | 1 | a0001c0001t0003g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1826+5929C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733477 | ||||||
| chr13:39733595
|
G | GT | 6 | a0001c0001t0004g0091a0002c0002t0002g0336a0002c0002t0002g0337others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+6058dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39733595 | |||||
| chr13:39733939
|
C | A | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+6391C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733939 | ||||||
| chr13:39733968
|
T | C | 4 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(1): Show | 4 | HG01515.hp2 HG01517.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826+6420T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733968 | ||||||
| chr13:39733980
|
C | T | 138 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1826+6432C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733980 | ||||||
| chr13:39734060
|
A | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+6512A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734060 | ||||||
| chr13:39734067
|
T | G | 1 | a0002c0002t0002g0352 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1826+6519T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734067 | ||||||
| chr13:39734170
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1826+6622T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734170 | ||||||
| chr13:39734289
|
G | A | 1 | a0004c0004t0002g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1826+6741G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734289 | ||||||
| chr13:39734426
|
T | C | 7 | a0001c0001t0003g0008a0001c0001t0003g0189a0002c0002t0003g0227others(4): Show | 8 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826+6878T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734426 | ||||||
| chr13:39734553
|
C | G | 175 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+7005C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734553 | ||||||
| chr13:39734613
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1826+7065C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734613 | ||||||
| chr13:39734625
|
A | C | 1 | a0001c0001t0015g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1826+7077A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734625 | ||||||
| chr13:39734684
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1826+7136C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734684 | ||||||
| chr13:39734924
|
A | G | 172 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1826+7376A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734924 | ||||||
| chr13:39734978
|
T | C | 1 | a0002c0002t0002g0281 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1826+7430T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734978 | ||||||
| chr13:39734985
|
A | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0189a0005c0005t0003g0015others(2): Show | 6 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+7437A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734985 | ||||||
| chr13:39735250
|
T | G | 2 | a0002c0002t0003g0227a0006c0008t0003g0226 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+7702T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735250 | ||||||
| chr13:39735418
|
G | GCTTT | 346 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(343): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1826+7872_1826+787 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39735418 | |||||
| chr13:39735657
|
G | A | 1 | a0002c0002t0002g0356 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1826+8109G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735657 | ||||||
| chr13:39735706
|
C | CT | 16 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(13): Show | 16 | HG01255.hp1 HG02056.hp2 HG03490.hp1 others(13): Show |
intron_variant | MODIFIER | c.1826+8177dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39735706 | |||||
| chr13:39735721
|
TTTTTG | T | 130 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1826+8174_1826+817 others(9): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735721 | ||||||
| chr13:39735722
|
TTTTG | T | 7 | a0001c0001t0004g0206a0002c0002t0002g0308a0002c0002t0002g0309others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+8175_1826+817 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735722 | ||||||
| chr13:39735808
|
T | A | 1 | a0001c0001t0004g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1826+8260T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735808 | ||||||
| chr13:39736009
|
G | A | 1 | a0001c0001t0003g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1826+8461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736009 | ||||||
| chr13:39736198
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+8650C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736198 | ||||||
| chr13:39736362
|
G | A | 3 | a0001c0001t0003g0019a0002c0002t0007g0306a0002c0002t0011g0012 | 4 | HG02572.hp1 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+8814G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736362 | ||||||
| chr13:39736373
|
G | A | 1 | a0002c0002t0002g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826+8825G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736373 | ||||||
| chr13:39736398
|
G | T | 1 | a0001c0001t0004g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1826+8850G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736398 | ||||||
| chr13:39736596
|
C | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+9048C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736596 | ||||||
| chr13:39736875
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1826+9327A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736875 | ||||||
| chr13:39737127
|
G | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0068a0001c0001t0003g0069others(1): Show | 5 | HG00423.hp1 NA18949.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826+9579G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737127 | ||||||
| chr13:39737148
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0176 | 2 | NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1826+9600C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737148 | ||||||
| chr13:39737163
|
G | A | 137 | a0001c0001t0004g0049a0001c0001t0004g0066a0001c0001t0004g0067others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1826+9615G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737163 | ||||||
| chr13:39737222
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0003g0063 | 2 | NA18979.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1826+9674A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737222 | ||||||
| chr13:39737231
|
C | T | 2 | a0001c0001t0003g0211a0001c0001t0003g0212 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1826+9683C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737231 | ||||||
| chr13:39737232
|
G | A | 1 | a0006c0008t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1826+9684G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737232 | ||||||
| chr13:39737253
|
C | T | 1 | a0002c0002t0002g0328 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1826+9705C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737253 | ||||||
| chr13:39737362
|
C | T | 5 | a0001c0001t0004g0091a0002c0002t0002g0336a0002c0002t0002g0337others(2): Show | 5 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826+9814C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737362 | ||||||
| chr13:39737468
|
C | G | 1 | a0002c0002t0002g0294 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1826+9920C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737468 | ||||||
| chr13:39737485
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1826+9937T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737485 | ||||||
| chr13:39737619
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1826+10071C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737619 | ||||||
| chr13:39737621
|
G | A | 22 | a0001c0001t0004g0085a0001c0001t0004g0086a0002c0002t0002g0246others(19): Show | 22 | HG00323.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1826+10073G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737621 | ||||||
| chr13:39737682
|
C | T | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1826+10134C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737682 | ||||||
| chr13:39737770
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1826+10222T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737770 | ||||||
| chr13:39737789
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 6 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+10241C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737789 | ||||||
| chr13:39737834
|
G | A | 9 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0204others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1826+10286G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737834 | ||||||
| chr13:39738009
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1826+10461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738009 | ||||||
| chr13:39738010
|
C | T | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0004c0004t0007g0253 | 3 | HG01515.hp1 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1826+10462C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738010 | ||||||
| chr13:39738207
|
T | C | 3 | a0001c0001t0003g0061a0001c0001t0003g0063a0001c0001t0003g0080 | 3 | NA18974.hp2 NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1826+10659T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738207 | ||||||
| chr13:39738367
|
T | A | 2 | a0002c0002t0002g0266a0002c0002t0002g0342 | 2 | NA18954.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1826+10819T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738367 | ||||||
| chr13:39738911
|
G | A | 175 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+11363G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738911 | ||||||
| chr13:39738959
|
G | A | 2 | a0005c0005t0003g0015a0005c0005t0003g0017 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1826+11411G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738959 | ||||||
| chr13:39739089
|
G | A | 92 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(89): Show | 99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+11541G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739089 | ||||||
| chr13:39739321
|
AT | A | 8 | a0002c0002t0002g0270a0002c0002t0002g0271a0002c0002t0002g0272others(5): Show | 8 | HG00609.hp2 HG02027.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1827-11622delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39739321 | |||||
| chr13:39739325
|
C | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(342): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1827-11621C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739325 | ||||||
| chr13:39739325
|
C | T | 1 | a0001c0001t0003g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1827-11621C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739325 | ||||||
| chr13:39739726
|
C | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1827-11220C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739726 | ||||||
| chr13:39739846
|
G | A | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0084 | 3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1827-11100G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739846 | ||||||
| chr13:39739851
|
T | C | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1827-11095T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739851 | ||||||
| chr13:39740032
|
A | G | 1 | a0001c0001t0004g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1827-10914A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740032 | ||||||
| chr13:39740119
|
A | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0037a0001c0001t0003g0046others(3): Show | 6 | HG02040.hp1 HG02071.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-10827A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740119 | ||||||
| chr13:39740223
|
T | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-10723T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740223 | ||||||
| chr13:39740272
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1827-10674G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740272 | ||||||
| chr13:39740630
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(342): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1827-10316G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740630 | ||||||
| chr13:39741038
|
A | C | 4 | a0001c0001t0003g0019a0002c0002t0003g0227a0002c0002t0007g0306others(1): Show | 4 | HG02572.hp1 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-9908A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741038 | ||||||
| chr13:39741132
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0162others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-9814A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741132 | ||||||
| chr13:39741143
|
A | G | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-9803A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741143 | ||||||
| chr13:39741288
|
G | C | 2 | a0002c0002t0004g0215a0002c0002t0004g0216 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1827-9658G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741288 | ||||||
| chr13:39741443
|
G | A | 92 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(89): Show | 99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1827-9503G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741443 | ||||||
| chr13:39741457
|
G | T | 1 | a0004c0004t0002g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1827-9489G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741457 | ||||||
| chr13:39741468
|
C | T | 6 | a0002c0002t0002g0248a0002c0002t0002g0249a0002c0002t0002g0250others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-9478C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741468 | ||||||
| chr13:39741473
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1827-9473A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741473 | ||||||
| chr13:39741546
|
T | C | 6 | a0002c0002t0002g0245a0002c0002t0002g0316a0002c0002t0002g0317others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-9400T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741546 | ||||||
| chr13:39742452
|
T | A | 1 | a0002c0002t0002g0352 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1827-8494T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742452 | ||||||
| chr13:39742467
|
G | A | 139 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0162others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-8479G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742467 | ||||||
| chr13:39742745
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-8201C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742745 | ||||||
| chr13:39742781
|
C | A | 9 | a0002c0002t0002g0230a0002c0002t0002g0232a0002c0002t0002g0234others(6): Show | 9 | HG01106.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1827-8165C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742781 | ||||||
| chr13:39742797
|
A | G | 1 | a0002c0002t0005g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1827-8149A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742797 | ||||||
| chr13:39742860
|
C | G | 7 | a0001c0001t0003g0028a0001c0001t0003g0031a0001c0001t0003g0064others(4): Show | 7 | HG02004.hp2 HG02735.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1827-8086C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742860 | ||||||
| chr13:39743212
|
A | G | 1 | a0002c0002t0002g0304 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1827-7734A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743212 | ||||||
| chr13:39743244
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1827-7702G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743244 | ||||||
| chr13:39743350
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1827-7596C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743350 | ||||||
| chr13:39743396
|
A | G | 1 | a0002c0002t0009g0277 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1827-7550A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743396 | ||||||
| chr13:39743434
|
A | C | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1827-7512A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743434 | ||||||
| chr13:39743838
|
G | A | 1 | a0001c0001t0005g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1827-7108G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743838 | ||||||
| chr13:39743945
|
T | C | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-7001T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743945 | ||||||
| chr13:39744155
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1827-6791C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744155 | ||||||
| chr13:39744156
|
A | G | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6790A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744156 | ||||||
| chr13:39744280
|
A | G | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6666A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744280 | ||||||
| chr13:39744317
|
C | T | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1827-6629C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744317 | ||||||
| chr13:39744371
|
A | G | 2 | a0002c0002t0002g0266a0002c0002t0002g0342 | 2 | NA18954.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1827-6575A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744371 | ||||||
| chr13:39744451
|
A | G | 173 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6495A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744451 | ||||||
| chr13:39744514
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-6432A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744514 | ||||||
| chr13:39744671
|
C | G | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-6275C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744671 | ||||||
| chr13:39744682
|
A | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1827-6264A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744682 | ||||||
| chr13:39744822
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1827-6124G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744822 | ||||||
| chr13:39744856
|
A | G | 1 | a0002c0002t0002g0356 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1827-6090A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744856 | ||||||
| chr13:39744960
|
C | T | 90 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(87): Show | 97 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1827-5986C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744960 | ||||||
| chr13:39744999
|
C | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-5947C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744999 | ||||||
| chr13:39745088
|
T | A | 230 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0162others(227): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1827-5858T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745088 | ||||||
| chr13:39745107
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1827-5839C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745107 | ||||||
| chr13:39745120
|
C | G | 139 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0162others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-5826C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745120 | ||||||
| chr13:39745206
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1827-5740A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745206 | ||||||
| chr13:39745784
|
G | C | 1 | a0002c0002t0007g0330 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1827-5162G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745784 | ||||||
| chr13:39745817
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1827-5129A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745817 | ||||||
| chr13:39746013
|
C | T | 1 | a0002c0002t0002g0296 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1827-4933C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746013 | ||||||
| chr13:39746026
|
T | C | 1 | a0002c0002t0002g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1827-4920T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746026 | ||||||
| chr13:39746335
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1827-4611G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746335 | ||||||
| chr13:39746346
|
A | G | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1827-4600A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746346 | ||||||
| chr13:39746401
|
C | T | 3 | a0001c0001t0003g0019a0002c0002t0007g0306a0002c0002t0011g0012 | 4 | HG02572.hp1 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-4545C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746401 | ||||||
| chr13:39746440
|
C | A | 4 | a0002c0002t0002g0239a0002c0002t0002g0240a0002c0002t0002g0293others(1): Show | 4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1827-4506C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746440 | ||||||
| chr13:39746543
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1827-4403C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746543 | ||||||
| chr13:39746738
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-4208A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746738 | ||||||
| chr13:39746793
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1827-4153T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746793 | ||||||
| chr13:39746847
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1827-4099T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746847 | ||||||
| chr13:39746970
|
C | T | 3 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0209 | 5 | HG01891.hp2 HG02109.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1827-3976C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746970 | ||||||
| chr13:39747093
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1827-3853C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747093 | ||||||
| chr13:39747161
|
G | C | 346 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(343): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1827-3785G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747161 | ||||||
| chr13:39747215
|
A | G | 72 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(69): Show | 76 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1827-3731A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747215 | ||||||
| chr13:39747272
|
T | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0189 | 3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1827-3674T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747272 | ||||||
| chr13:39747340
|
G | A | 353 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1827-3606G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747340 | ||||||
| chr13:39747419
|
C | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0172a0002c0002t0004g0221 | 3 | HG02280.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1827-3527C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747419 | ||||||
| chr13:39747485
|
G | A | 4 | a0002c0002t0002g0308a0002c0002t0002g0310a0002c0002t0002g0311others(1): Show | 4 | HG02258.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-3461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747485 | ||||||
| chr13:39747626
|
C | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-3320C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747626 | ||||||
| chr13:39747657
|
T | C | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1827-3289T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747657 | ||||||
| chr13:39747691
|
T | C | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1827-3255T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747691 | ||||||
| chr13:39747709
|
A | G | 1 | a0002c0002t0002g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1827-3237A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747709 | ||||||
| chr13:39747863
|
G | A | 1 | a0001c0011t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1827-3083G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747863 | ||||||
| chr13:39747890
|
G | GTTAAATA others(12): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1827-3055_1827-303 others(23): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39747890 | |||||
| chr13:39747958
|
T | C | 143 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1827-2988T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747958 | ||||||
| chr13:39748002
|
T | A | 3 | a0005c0005t0003g0015a0005c0005t0003g0016a0005c0005t0003g0017 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1827-2944T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748002 | ||||||
| chr13:39748353
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-2593G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748353 | ||||||
| chr13:39748424
|
T | G | 174 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0090others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1827-2522T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748424 | ||||||
| chr13:39748560
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-2386A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748560 | ||||||
| chr13:39748569
|
C | G | 2 | a0002c0002t0010g0223a0007c0009t0010g0222 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1827-2377C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748569 | ||||||
| chr13:39748590
|
G | T | 1 | a0003c0003t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1827-2356G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748590 | ||||||
| chr13:39748622
|
G | GA | 7 | a0001c0001t0003g0048a0001c0001t0003g0052a0001c0001t0003g0053others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1827-2312dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39748622 | |||||
| chr13:39749049
|
T | C | 91 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(88): Show | 98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1827-1897T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749049 | ||||||
| chr13:39749070
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1876C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749070 | ||||||
| chr13:39749072
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1874C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749072 | ||||||
| chr13:39749073
|
A | T | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1873A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749073 | ||||||
| chr13:39749074
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1872A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749074 | ||||||
| chr13:39749101
|
C | T | 139 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1845C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749101 | ||||||
| chr13:39749306
|
C | T | 139 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1640C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749306 | ||||||
| chr13:39749314
|
T | A | 139 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1632T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749314 | ||||||
| chr13:39749399
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1827-1547T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749399 | ||||||
| chr13:39749751
|
A | G | 1 | a0002c0007t0002g0300 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1827-1195A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749751 | ||||||
| chr13:39749796
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1827-1150G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749796 | ||||||
| chr13:39750081
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0173 | 2 | HG03491.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1827-865A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750081 | ||||||
| chr13:39750614
|
G | A | 1 | a0002c0002t0003g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-332G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750614 | ||||||
| chr13:39750659
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1827-287T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750659 | ||||||
| chr13:39750782
|
C | G | 1 | a0002c0002t0002g0349 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1827-164C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750782 |