geneid | 8292 |
---|---|
ensemblid | ENSG00000206561.14 |
hgncid | 2226 |
symbol | COLQ |
name | collagen like tail subunit of asymmetric acetylcholinesterase |
refseq_nuc | NM_005677.4 |
refseq_prot | NP_005668.2 |
ensembl_nuc | ENST00000383788.10 |
ensembl_prot | ENSP00000373298.3 |
mane_status | MANE Select |
chr | chr3 |
start | 15450133 |
end | 15521706 |
strand | - |
ver | v1.2 |
region | chr3:15450133-15521706 |
region5000 | chr3:15445133-15526706 |
regionname0 | COLQ_chr3_15450133_15521706 |
regionname5000 | COLQ_chr3_15445133_15526706 |
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 | 455 | 355 | 69 | 66 | 172 | 12 | 34 | 134 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0002 | 0/0 | 455 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0003 | 0/0 | 455 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0004 | 0/0 | 455 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0005 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0006 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
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 | 1368 | 338 | 56 | 63 | 171 | 12 | 34 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0002 | 0/0 | 1368 | 17 | 17 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0003 | 0/0 | 1368 | 14 | 13 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0004 | 0/0 | 1368 | 6 | 6 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0005 | 0/0 | 1368 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0006 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0007 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0008 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
c0009 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1593 | 160 | 30 | 38 | 67 | 7 | 17 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0002 | 0/1 | 1593 | 88 | 17 | 17 | 39 | 5 | 9 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0003 | 0/0 | 1593 | 76 | 7 | 10 | 53 | 0 | 6 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0004 | 0/0 | 1593 | 16 | 13 | 1 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0005 | 0/0 | 1593 | 16 | 14 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0006 | 0/0 | 1593 | 8 | 1 | 0 | 6 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0007 | 0/0 | 1593 | 4 | 0 | 0 | 4 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0008 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0009 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0010 | 0/0 | 1593 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0011 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0012 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0013 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0014 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0015 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0016 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
t0017 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
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 | 5 | 0 | 2 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
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 | 1368 | 338 | 56 | 63 | 171 | 12 | 34 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0003 | 0/0 | 1368 | 14 | 13 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0005 | 0/0 | 1368 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0008 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0002c0002 | 0/0 | 1368 | 17 | 17 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0003c0004 | 0/0 | 1368 | 6 | 6 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0004c0006 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0005c0009 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0006c0007 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2960 | 157 | 30 | 36 | 66 | 7 | 17 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0002 | 0/1 | 2960 | 82 | 11 | 17 | 39 | 5 | 9 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0003 | 0/0 | 2960 | 76 | 7 | 10 | 53 | 0 | 6 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0006 | 0/0 | 2960 | 8 | 1 | 0 | 6 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0007 | 0/0 | 2960 | 4 | 0 | 0 | 4 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0009 | 0/0 | 2960 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0010 | 0/0 | 2960 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0011 | 0/0 | 2960 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0012 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0013 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0014 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0015 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0016 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0001t0017 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0003t0004 | 0/0 | 2960 | 14 | 13 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0005t0005 | 0/0 | 2960 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0001c0008t0001 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0002c0002t0005 | 0/0 | 2960 | 14 | 14 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0002c0002t0008 | 0/0 | 2960 | 3 | 3 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0003c0004t0002 | 0/0 | 2960 | 6 | 6 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0004c0006t0004 | 0/0 | 2960 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0005c0009t0001 | 0/0 | 2960 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
a0006c0007t0001 | 0/0 | 2960 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | copy fasta | chr3 | 15445133 | 15526706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0009g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0013g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0016g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0001t0017g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0005t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0005t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0001c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0002c0002t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0003c0004t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0003c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0003c0004t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0003c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0003c0004t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0004c0006t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0004c0006t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0005c0009t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
a0006c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01071 | hp1 | a0006 | c0007 | t0001 | g0158 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01109 | hp2 | a0001 | c0003 | t0004 | g0327 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01168 | hp2 | a0001 | c0005 | t0005 | g0265 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01169 | hp1 | a0001 | c0005 | t0005 | g0264 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01361 | hp2 | a0005 | c0009 | t0001 | g0344 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01884 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0331 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02280 | hp1 | a0002 | c0002 | t0005 | g0251 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02280 | hp2 | a0002 | c0002 | t0005 | g0334 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0340 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02622 | hp2 | a0003 | c0004 | t0002 | g0257 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0291 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02647 | hp1 | a0001 | c0001 | t0013 | g0328 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02717 | hp1 | a0002 | c0002 | t0005 | g0252 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0341 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02723 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0332 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02809 | hp1 | a0002 | c0002 | t0005 | g0333 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0116 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02818 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0272 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02896 | hp1 | a0001 | c0003 | t0004 | g0028 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02922 | hp1 | a0002 | c0002 | t0005 | g0254 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02922 | hp2 | a0001 | c0003 | t0004 | g0028 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02970 | hp2 | a0002 | c0002 | t0008 | g0269 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02976 | hp1 | a0002 | c0002 | t0008 | g0270 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0259 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03041 | hp2 | a0001 | c0003 | t0004 | g0335 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03098 | hp1 | a0003 | c0004 | t0002 | g0247 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0339 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03139 | hp2 | a0001 | c0003 | t0004 | g0311 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03195 | hp2 | a0001 | c0003 | t0004 | g0123 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03209 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0268 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03516 | hp1 | a0003 | c0004 | t0002 | g0256 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0050 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03927 | hp1 | a0001 | c0001 | t0011 | g0068 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18522 | hp1 | a0002 | c0002 | t0005 | g0249 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18522 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18612 | hp2 | a0001 | c0008 | t0001 | g0190 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0255 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18942 | hp1 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18971 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18972 | hp1 | a0004 | c0006 | t0004 | g0246 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18973 | hp2 | a0001 | c0001 | t0017 | g0290 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18999 | hp2 | a0004 | c0006 | t0004 | g0244 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19006 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19043 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0342 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19086 | hp2 | a0001 | c0001 | t0009 | g0019 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19090 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19240 | hp1 | a0002 | c0002 | t0008 | g0271 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | GIH | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02109 | hp1 | a0002 | c0002 | t0005 | g0253 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02559 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03471 | hp1 | a0003 | c0004 | t0002 | g0258 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG03471 | hp2 | a0002 | c0002 | t0005 | g0336 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA18955 | hp2 | a0001 | c0001 | t0009 | g0019 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20300 | hp1 | a0002 | c0002 | t0005 | g0266 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
NA21309 | hp2 | a0001 | c0003 | t0004 | g0337 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0155 | REF | REF | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0215 | REF | REF | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15455977
|
C | T | 1 | a0006 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.1117G>A | p.Gly373Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1198/2960 | 1117/1368 | 373/455 | chr3 | 15455977 | ||
chr3:15455986
|
C | T | 1 | a0003 | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
missense_variant | MODERATE | c.1108G>A | p.Asp370Asn | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1189/2960 | 1108/1368 | 370/455 | chr3 | 15455986 | ||
chr3:15456013
|
G | A | 1 | a0004 | 2 | NA18972.hp1 NA18999.hp2 |
missense_variant | MODERATE | c.1081C>T | p.Pro361Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1162/2960 | 1081/1368 | 361/455 | chr3 | 15456013 | ||
chr3:15458206
|
T | C | 1 | a0002 | 17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
missense_variant | MODERATE | c.934A>G | p.Ser312Gly | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/17 | 1015/2960 | 934/1368 | 312/455 | chr3 | 15458206 | ||
chr3:15521603
|
G | C | 1 | a0005 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.23C>G | p.Thr8Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/17 | 104/2960 | 23/1368 | 8/455 | chr3 | 15521603 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15451674
|
G | T | 1 | a0001c0003 | 14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
synonymous_variant | LOW | c.1338C>A | p.Ile446Ile | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1419/2960 | 1338/1368 | 446/455 | chr3 | 15451674 | ||
chr3:15453879
|
G | A | 1 | a0001c0005 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.1248C>T | p.Asp416Asp | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/17 | 1329/2960 | 1248/1368 | 416/455 | chr3 | 15453879 | ||
chr3:15488227
|
G | A | 1 | a0001c0008 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.300C>T | p.Ser100Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/17 | 381/2960 | 300/1368 | 100/455 | chr3 | 15488227 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15450237
|
C | T | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1407 | chr3 | 15450237 | |||||
chr3:15450249
|
G | A | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(6): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1395C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1395 | chr3 | 15450249 | |||||
chr3:15450258
|
T | C | 1 | a0001c0001t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1386 | chr3 | 15450258 | |||||
chr3:15450364
|
G | A | 1 | a0001c0001t0007 | 4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1280 | chr3 | 15450364 | |||||
chr3:15450571
|
C | T | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1073 | chr3 | 15450571 | |||||
chr3:15450643
|
C | T | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(6): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1001G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1001 | chr3 | 15450643 | |||||
chr3:15450646
|
G | A | 1 | a0001c0001t0017 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 998 | chr3 | 15450646 | |||||
chr3:15450650
|
C | T | 1 | a0002c0002t0008 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*994G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 994 | chr3 | 15450650 | |||||
chr3:15450699
|
C | T | 1 | a0001c0001t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 945 | chr3 | 15450699 | |||||
chr3:15450796
|
G | A | 1 | a0001c0001t0011 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 848 | chr3 | 15450796 | |||||
chr3:15450838
|
G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*806C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 806 | chr3 | 15450838 | |||||
chr3:15450893
|
G | A | 1 | a0001c0001t0009 | 2 | NA18955.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*751C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 751 | chr3 | 15450893 | |||||
chr3:15451129
|
G | A | 4 | a0001c0001t0013a0001c0005t0005a0002c0002t0005others(1): Show | 20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 515 | chr3 | 15451129 | |||||
chr3:15451152
|
C | T | 1 | a0001c0001t0010 | 2 | HG03041.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 492 | chr3 | 15451152 | |||||
chr3:15451223
|
C | T | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 421 | chr3 | 15451223 | |||||
chr3:15451279
|
T | A | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(10): Show | 191 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*365A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 365 | chr3 | 15451279 | |||||
chr3:15451300
|
G | A | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(12): Show | 207 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 344 | chr3 | 15451300 | |||||
chr3:15521671
|
C | T | 3 | a0001c0001t0003a0001c0001t0006a0001c0001t0011 | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/17 | 46 | chr3 | 15521671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15451744
|
C | T | 3 | a0001c0001t0010g0259a0001c0001t0010g0342a0001c0001t0016g0255 | 3 | HG03041.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1299-31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451744 | ||||||
chr3:15451772
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0032a0001c0001t0003g0090 | 5 | HG00423.hp1 NA18952.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299-59A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451772 | ||||||
chr3:15451874
|
G | C | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1299-161C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451874 | ||||||
chr3:15452025
|
C | T | 18 | a0001c0001t0013g0328a0001c0005t0005g0264a0001c0005t0005g0265others(15): Show | 20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299-312G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452025 | ||||||
chr3:15452068
|
A | AT | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(72): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1299-356dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | ||||||
chr3:15452068
|
AT | A | 34 | a0001c0001t0001g0097a0001c0001t0002g0293a0001c0001t0003g0047others(31): Show | 37 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1299-356delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | ||||||
chr3:15452068
|
ATT | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(184): Show | 214 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.1299-357_1299-356d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | ||||||
chr3:15452141
|
A | C | 3 | a0001c0001t0010g0259a0001c0001t0010g0342a0001c0001t0016g0255 | 3 | HG03041.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1299-428T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452141 | ||||||
chr3:15452160
|
A | G | 21 | a0001c0001t0010g0259a0001c0001t0010g0342a0001c0001t0013g0328others(18): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1299-447T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452160 | ||||||
chr3:15452287
|
G | A | 13 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(10): Show | 14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1299-574C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452287 | ||||||
chr3:15452311
|
C | T | 150 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(147): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1299-598G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452311 | ||||||
chr3:15452484
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1299-771G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452484 | ||||||
chr3:15452495
|
G | A | 141 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(138): Show | 161 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1299-782C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452495 | ||||||
chr3:15452522
|
C | T | 2 | a0001c0001t0002g0292a0001c0001t0014g0291 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1299-809G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452522 | ||||||
chr3:15452546
|
T | C | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1299-833A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452546 | ||||||
chr3:15452568
|
G | A | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299-855C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452568 | ||||||
chr3:15452635
|
G | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1299-922C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452635 | ||||||
chr3:15452734
|
G | C | 18 | a0001c0001t0013g0328a0001c0005t0005g0264a0001c0005t0005g0265others(15): Show | 20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299-1021C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452734 | ||||||
chr3:15452772
|
G | A | 147 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(144): Show | 168 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1298+1057C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452772 | ||||||
chr3:15453151
|
C | G | 142 | a0001c0001t0001g0274a0001c0001t0002g0016a0001c0001t0002g0017others(139): Show | 162 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1298+678G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453151 | ||||||
chr3:15453210
|
G | A | 2 | a0001c0001t0010g0259a0001c0001t0010g0342 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1298+619C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453210 | ||||||
chr3:15453232
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1298+597T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453232 | ||||||
chr3:15453252
|
C | A | 18 | a0001c0001t0013g0328a0001c0005t0005g0264a0001c0005t0005g0265others(15): Show | 20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1298+577G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453252 | ||||||
chr3:15453294
|
C | G | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1298+535G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453294 | ||||||
chr3:15453638
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0177a0001c0001t0001g0234others(1): Show | 4 | NA18966.hp1 NA19012.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298+191C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453638 | ||||||
chr3:15453794
|
G | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(51): Show | 61 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.1298+35C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453794 | ||||||
chr3:15453976
|
G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1196-45C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15453976 | ||||||
chr3:15454016
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1196-85C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454016 | ||||||
chr3:15454137
|
T | C | 154 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(151): Show | 175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1196-206A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454137 | ||||||
chr3:15454147
|
A | G | 154 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(151): Show | 175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1196-216T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454147 | ||||||
chr3:15454152
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(25): Show | 34 | HG00639.hp1 HG01891.hp1 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.1196-221G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454152 | ||||||
chr3:15454180
|
G | C | 1 | a0001c0008t0001g0190 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1196-249C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454180 | ||||||
chr3:15454257
|
G | A | 154 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(151): Show | 175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1196-326C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454257 | ||||||
chr3:15454333
|
T | C | 187 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(184): Show | 211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.1196-402A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454333 | ||||||
chr3:15454419
|
T | C | 92 | a0001c0001t0002g0017a0001c0001t0002g0023a0001c0001t0002g0024others(89): Show | 108 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1196-488A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454419 | ||||||
chr3:15454430
|
A | G | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1196-499T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454430 | ||||||
chr3:15454445
|
T | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0006g0054others(1): Show | 4 | HG00597.hp1 NA18994.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196-514A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454445 | ||||||
chr3:15454596
|
ACAGT | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(1): Show | 4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-669_1196-666d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454596 | ||||||
chr3:15454614
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | NA18942.hp1 NA18948.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-683G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454614 | ||||||
chr3:15454639
|
T | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(1): Show | 4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-708A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454639 | ||||||
chr3:15454651
|
G | GT | 28 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0103others(25): Show | 28 | HG00597.hp1 HG01071.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1196-721dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454651
|
G | GTTT | 24 | a0001c0001t0010g0259a0001c0003t0004g0028a0001c0003t0004g0121others(21): Show | 26 | HG01109.hp2 HG01168.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1196-723_1196-721d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454651
|
G | GTTTT | 8 | a0001c0003t0004g0331a0001c0003t0004g0335a0001c0003t0004g0339others(5): Show | 9 | HG01169.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1196-724_1196-721d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454651
|
GTTTTTTT | G | 104 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(101): Show | 119 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1196-727_1196-721d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454651
|
GTTTTTTT others(1): Show |
G | 35 | a0001c0001t0002g0024a0001c0001t0002g0098a0001c0001t0002g0198others(32): Show | 40 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1196-728_1196-721d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454651
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1196-730_1196-721d others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | ||||||
chr3:15454658
|
T | TA | 4 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(1): Show | 4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-728_1196-727i others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454658 | ||||||
chr3:15454664
|
T | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1196-733A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454664 | ||||||
chr3:15454763
|
C | T | 2 | a0001c0001t0010g0259a0001c0001t0010g0342 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1196-832G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454763 | ||||||
chr3:15454803
|
G | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(1): Show | 4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-872C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454803 | ||||||
chr3:15454836
|
T | A | 9 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0001t0010g0342others(6): Show | 10 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-905A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454836 | ||||||
chr3:15455001
|
T | G | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1195+898A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455001 | ||||||
chr3:15455040
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1195+859A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455040 | ||||||
chr3:15455046
|
C | A | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1195+853G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455046 | ||||||
chr3:15455332
|
C | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1195+567G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455332 | ||||||
chr3:15455359
|
CA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(74): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1195+539delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455359 | ||||||
chr3:15455561
|
G | C | 1 | a0001c0001t0003g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1195+338C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455561 | ||||||
chr3:15455571
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1195+328G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455571 | ||||||
chr3:15455680
|
C | T | 13 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(10): Show | 14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1195+219G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455680 | ||||||
chr3:15455754
|
G | A | 9 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0001t0010g0342others(6): Show | 10 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195+145C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455754 | ||||||
chr3:15455818
|
C | A | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1195+81G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455818 | ||||||
chr3:15456101
|
A | G | 41 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0001t0013g0328others(38): Show | 45 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1075-82T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456101 | ||||||
chr3:15456222
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0063a0001c0001t0003g0065 | 5 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-203T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456222 | ||||||
chr3:15456256
|
T | TCAGAGAG others(25): Show |
13 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0123others(10): Show | 14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074+172_1074+203d others(34): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456256 | ||||||
chr3:15456274
|
T | A | 2 | a0001c0001t0001g0208a0001c0001t0006g0050 | 2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1074+186A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456274 | ||||||
chr3:15456406
|
A | T | 1 | a0001c0001t0002g0282 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1074+54T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456406 | ||||||
chr3:15456754
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(201): Show | 232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.955-175A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456754 | ||||||
chr3:15456765
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(171): Show | 200 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.955-186C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456765 | ||||||
chr3:15456827
|
TTTCTTTT others(1): Show |
T | 170 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(167): Show | 196 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.955-256_955-249del others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456827 | ||||||
chr3:15456835
|
G | T | 54 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(51): Show | 58 | HG01081.hp2 HG01109.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.955-256C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456835 | ||||||
chr3:15456839
|
T | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.955-260A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456839 | ||||||
chr3:15456891
|
C | T | 4 | a0001c0001t0003g0010a0001c0001t0003g0037a0001c0001t0003g0052others(1): Show | 5 | NA18950.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-312G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456891 | ||||||
chr3:15456918
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(26): Show | 35 | HG00639.hp1 HG01891.hp1 HG01928.hp1 others(32): Show |
intron_variant | MODIFIER | c.955-339C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456918 | ||||||
chr3:15456947
|
C | T | 1 | a0001c0001t0003g0010 | 2 | NA18950.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.955-368G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456947 | ||||||
chr3:15456963
|
C | T | 1 | a0001c0001t0006g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.955-384G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456963 | ||||||
chr3:15457039
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-460A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457039 | ||||||
chr3:15457100
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.955-521T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457100 | ||||||
chr3:15457108
|
G | C | 2 | a0001c0001t0010g0259a0001c0003t0004g0327 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.955-529C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457108 | ||||||
chr3:15457241
|
A | G | 17 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(14): Show | 18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-662T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457241 | ||||||
chr3:15457259
|
T | C | 1 | a0002c0002t0005g0251 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-680A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457259 | ||||||
chr3:15457424
|
T | C | 1 | a0001c0001t0003g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.954+762A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457424 | ||||||
chr3:15457541
|
A | AT | 6 | a0001c0001t0002g0343a0003c0004t0002g0022a0003c0004t0002g0247others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+644dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457541 | ||||||
chr3:15457623
|
C | CTTTTTTT | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(169): Show | 198 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.954+556_954+562dup others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | ||||||
chr3:15457623
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0002g0297a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG02055.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.954+562_954+563ins others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | ||||||
chr3:15457623
|
C | CTTTTTTT others(3): Show |
17 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(14): Show | 18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+562_954+563ins others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | ||||||
chr3:15457673
|
T | C | 17 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(14): Show | 18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+513A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457673 | ||||||
chr3:15457749
|
A | T | 2 | a0001c0001t0010g0259a0001c0003t0004g0327 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.954+437T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457749 | ||||||
chr3:15457768
|
G | A | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+418C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457768 | ||||||
chr3:15457770
|
G | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0147a0001c0001t0001g0229others(3): Show | 6 | HG01891.hp2 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+416C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457770 | ||||||
chr3:15457823
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(171): Show | 200 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.954+363G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457823 | ||||||
chr3:15457951
|
T | C | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+235A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457951 | ||||||
chr3:15458568
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.815-243C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458568 | ||||||
chr3:15458741
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(223): Show | 256 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.815-416A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458741 | ||||||
chr3:15458788
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(184): Show | 214 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.815-463G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458788 | ||||||
chr3:15458846
|
A | AT | 17 | a0001c0001t0001g0103a0001c0001t0001g0168a0001c0001t0001g0248others(14): Show | 18 | HG00733.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-522dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458846 | ||||||
chr3:15458846
|
A | ATT | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.815-523_815-522dup others(2): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458846 | ||||||
chr3:15458879
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.815-554A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458879 | ||||||
chr3:15458906
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-581G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458906 | ||||||
chr3:15458984
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.815-659G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458984 | ||||||
chr3:15459063
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-738G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459063 | ||||||
chr3:15459196
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815-871G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459196 | ||||||
chr3:15459231
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815-906G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459231 | ||||||
chr3:15459249
|
G | A | 4 | a0001c0001t0007g0187a0001c0001t0007g0206a0001c0001t0007g0207others(1): Show | 4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-924C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459249 | ||||||
chr3:15459261
|
A | G | 2 | a0003c0004t0002g0257a0003c0004t0002g0258 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.815-936T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459261 | ||||||
chr3:15459389
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(187): Show | 217 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.815-1064G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459389 | ||||||
chr3:15459426
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(174): Show | 204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.815-1101G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459426 | ||||||
chr3:15459449
|
A | T | 15 | a0001c0001t0010g0259a0001c0003t0004g0028a0001c0003t0004g0121others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-1124T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459449 | ||||||
chr3:15459478
|
C | CT | 21 | a0001c0001t0001g0105a0001c0001t0001g0233a0001c0001t0001g0248others(18): Show | 23 | HG01123.hp2 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.815-1154dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459478 | ||||||
chr3:15459478
|
CTT | C | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-1155_815-1154d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459478 | ||||||
chr3:15459518
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.815-1193C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459518 | ||||||
chr3:15459564
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.815-1239G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459564 | ||||||
chr3:15459580
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.815-1255C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459580 | ||||||
chr3:15459635
|
G | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(201): Show | 232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.815-1310C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459635 | ||||||
chr3:15459646
|
T | C | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(6): Show | 9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-1321A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459646 | ||||||
chr3:15459791
|
T | TTTA | 143 | a0001c0001t0001g0274a0001c0001t0002g0016a0001c0001t0002g0017others(140): Show | 163 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.815-1469_815-1467d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | ||||||
chr3:15459791
|
T | TTTATTA | 13 | a0001c0001t0003g0081a0001c0003t0004g0028a0001c0003t0004g0121others(10): Show | 14 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.815-1472_815-1467d others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | ||||||
chr3:15459791
|
TTTA | T | 8 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(5): Show | 8 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.815-1469_815-1467d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | ||||||
chr3:15459799
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0193 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.815-1474A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459799 | ||||||
chr3:15459942
|
T | C | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.815-1617A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459942 | ||||||
chr3:15459985
|
A | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0154a0001c0001t0002g0163 | 4 | HG00642.hp1 HG01517.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-1660T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459985 | ||||||
chr3:15460088
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.815-1763T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460088 | ||||||
chr3:15460179
|
C | T | 53 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0026others(50): Show | 57 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.815-1854G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460179 | ||||||
chr3:15460287
|
G | A | 12 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(9): Show | 13 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.815-1962C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460287 | ||||||
chr3:15460301
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(218): Show | 251 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(248): Show |
intron_variant | MODIFIER | c.815-1976T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460301 | ||||||
chr3:15460504
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.815-2179C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460504 | ||||||
chr3:15460623
|
A | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(201): Show | 232 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.815-2298T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460623 | ||||||
chr3:15460713
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.815-2388G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460713 | ||||||
chr3:15460738
|
T | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815-2413A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460738 | ||||||
chr3:15460886
|
T | C | 10 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(7): Show | 10 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.815-2561A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460886 | ||||||
chr3:15461091
|
C | T | 8 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(5): Show | 8 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.815-2766G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461091 | ||||||
chr3:15461174
|
G | T | 76 | a0001c0001t0001g0115a0001c0001t0001g0131a0001c0001t0001g0132others(73): Show | 79 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.815-2849C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461174 | ||||||
chr3:15461177
|
T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.815-2852A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461177 | ||||||
chr3:15461189
|
T | TCCCCGCC others(1): Show |
19 | a0001c0001t0001g0221a0001c0001t0001g0274a0001c0001t0002g0026others(16): Show | 20 | HG00558.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.815-2865_815-2864i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | ||||||
chr3:15461189
|
T | TCCCCGCC others(2): Show |
15 | a0001c0001t0001g0203a0001c0001t0002g0027a0001c0001t0002g0279others(12): Show | 16 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-2865_815-2864i others(11): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | ||||||
chr3:15461189
|
T | TCCCCGCC others(3): Show |
1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.815-2865_815-2864i others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | ||||||
chr3:15461190
|
C | CCCCGCA | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-2866_815-2865i others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461190 | ||||||
chr3:15461198
|
G | C | 60 | a0001c0001t0001g0203a0001c0001t0001g0221a0001c0001t0001g0274others(57): Show | 63 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.815-2873C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461198 | ||||||
chr3:15461258
|
C | T | 6 | a0001c0001t0001g0118a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-2933G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461258 | ||||||
chr3:15461353
|
G | C | 74 | a0001c0001t0001g0170a0001c0001t0001g0195a0001c0001t0001g0196others(71): Show | 80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.815-3028C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461353 | ||||||
chr3:15461493
|
G | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815-3168C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461493 | ||||||
chr3:15461548
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(216): Show | 249 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.815-3223C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461548 | ||||||
chr3:15461704
|
C | T | 5 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(2): Show | 5 | NA18987.hp1 NA19009.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-3379G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461704 | ||||||
chr3:15461745
|
T | C | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3420A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461745 | ||||||
chr3:15461873
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.815-3548A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461873 | ||||||
chr3:15461940
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.815-3615A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461940 | ||||||
chr3:15461998
|
C | CTTAT | 57 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0113others(54): Show | 63 | HG00280.hp2 HG00597.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.815-3677_815-3674d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | ||||||
chr3:15461998
|
C | CTTATTTA others(1): Show |
3 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0243 | 3 | HG02257.hp1 HG02451.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.815-3681_815-3674d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | ||||||
chr3:15461998
|
CTTAT | C | 10 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.815-3677_815-3674d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | ||||||
chr3:15461998
|
CTTATTTA others(13): Show |
C | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3693_815-3674d others(22): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | ||||||
chr3:15462017
|
A | ATTTG | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(174): Show | 201 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.815-3693_815-3692i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462017 | ||||||
chr3:15462017
|
A | G | 1 | a0001c0001t0003g0013 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.815-3692T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462017 | ||||||
chr3:15462021
|
A | ATTTG | 10 | a0001c0001t0002g0343a0001c0001t0010g0259a0002c0002t0008g0269others(7): Show | 11 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.815-3697_815-3696i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | ||||||
chr3:15462021
|
A | ATTTGTTT others(1): Show |
3 | a0001c0001t0002g0025a0001c0001t0002g0287a0001c0001t0003g0075 | 4 | HG00544.hp1 HG02818.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-3697_815-3696i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | ||||||
chr3:15462021
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(175): Show | 203 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.815-3696T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | ||||||
chr3:15462025
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.815-3700T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462025 | ||||||
chr3:15462029
|
A | G | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.815-3704T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462029 | ||||||
chr3:15462068
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(190): Show | 220 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.815-3743C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462068 | ||||||
chr3:15462076
|
G | A | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.815-3751C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462076 | ||||||
chr3:15462111
|
C | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-3786G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462111 | ||||||
chr3:15462303
|
T | G | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3978A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462303 | ||||||
chr3:15462325
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.815-4000G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462325 | ||||||
chr3:15462437
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(27): Show | 36 | HG00639.hp1 HG01515.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.814+3904C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462437 | ||||||
chr3:15462492
|
C | CG | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+3848dupC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462492 | ||||||
chr3:15462706
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+3635T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462706 | ||||||
chr3:15463107
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0125a0001c0001t0015g0116 | 4 | HG02258.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+3234G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463107 | ||||||
chr3:15463150
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.814+3191G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463150 | ||||||
chr3:15463231
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+3110G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463231 | ||||||
chr3:15463277
|
AT | A | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(340): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.814+3063delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463277 | ||||||
chr3:15463315
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(187): Show | 217 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.814+3026C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463315 | ||||||
chr3:15463320
|
G | GT | 9 | a0001c0001t0002g0130a0001c0001t0002g0242a0001c0001t0002g0293others(6): Show | 9 | HG01928.hp2 HG01943.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.814+3020dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463320 | ||||||
chr3:15463321
|
T | G | 21 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(18): Show | 22 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.814+3020A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463321 | ||||||
chr3:15463339
|
GTTGTTTT | G | 16 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(13): Show | 17 | HG02055.hp1 HG02280.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.814+2995_814+3001d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463339 | ||||||
chr3:15463440
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.814+2901C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463440 | ||||||
chr3:15463446
|
A | G | 1 | a0001c0001t0017g0290 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.814+2895T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463446 | ||||||
chr3:15463472
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.814+2869T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463472 | ||||||
chr3:15463536
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(208): Show | 239 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.814+2805A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463536 | ||||||
chr3:15463598
|
G | A | 3 | a0001c0001t0001g0212a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG02630.hp1 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.814+2743C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463598 | ||||||
chr3:15463717
|
C | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(180): Show | 209 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.814+2624G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463717 | ||||||
chr3:15463736
|
G | A | 8 | a0002c0002t0005g0020a0002c0002t0005g0021a0002c0002t0005g0249others(5): Show | 10 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.814+2605C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463736 | ||||||
chr3:15463844
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0193 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.814+2497G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463844 | ||||||
chr3:15463898
|
T | C | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+2443A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463898 | ||||||
chr3:15463923
|
G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+2418C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463923 | ||||||
chr3:15463941
|
T | C | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+2400A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463941 | ||||||
chr3:15463993
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+2348T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463993 | ||||||
chr3:15464003
|
G | A | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+2338C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464003 | ||||||
chr3:15464124
|
G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814+2217C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464124 | ||||||
chr3:15464138
|
A | AG | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(207): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.814+2202dupC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464138 | ||||||
chr3:15464175
|
A | C | 9 | a0001c0001t0002g0343a0002c0002t0008g0269a0002c0002t0008g0270others(6): Show | 10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.814+2166T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464175 | ||||||
chr3:15464393
|
A | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+1948T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464393 | ||||||
chr3:15464469
|
C | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+1872G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464469 | ||||||
chr3:15464538
|
C | T | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+1803G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464538 | ||||||
chr3:15464718
|
A | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+1623T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464718 | ||||||
chr3:15464747
|
G | C | 54 | a0001c0001t0001g0274a0001c0001t0002g0016a0001c0001t0002g0025others(51): Show | 58 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.814+1594C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464747 | ||||||
chr3:15464795
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.814+1546A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464795 | ||||||
chr3:15464935
|
G | A | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+1406C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464935 | ||||||
chr3:15464971
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.814+1370G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464971 | ||||||
chr3:15465032
|
G | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+1309C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465032 | ||||||
chr3:15465035
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(26): Show | 35 | HG00639.hp1 HG01515.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.814+1306C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465035 | ||||||
chr3:15465042
|
A | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(207): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.814+1299T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465042 | ||||||
chr3:15465168
|
C | T | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(340): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.814+1173G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465168 | ||||||
chr3:15465179
|
C | CA | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(340): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.814+1161dupT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465179 | ||||||
chr3:15465220
|
C | CAGACTTT others(60): Show |
1 | a0003c0004t0002g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.814+1120_814+1121i others(69): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465220 | ||||||
chr3:15465220
|
C | CAGACTTT others(56): Show |
1 | a0003c0004t0002g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.814+1120_814+1121i others(65): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465220 | ||||||
chr3:15465232
|
T | TTTTA | 65 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0119others(62): Show | 67 | HG00280.hp1 HG00621.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.814+1108_814+1109i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
T | TTTTATTT others(1): Show |
12 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0214others(9): Show | 13 | HG00597.hp2 HG01099.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+1108_814+1109i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
T | TTTTATTT others(64): Show |
1 | a0003c0004t0002g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.814+1108_814+1109i others(73): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
T | TTTTATTT others(56): Show |
3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.814+1108_814+1109i others(65): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
TTTGA | T | 38 | a0001c0001t0001g0092a0001c0001t0001g0170a0001c0001t0001g0184others(35): Show | 43 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.814+1105_814+1108d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
TTTGATTT others(1): Show |
T | 20 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(17): Show | 20 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.814+1101_814+1108d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
TTTGATTT others(5): Show |
T | 2 | a0001c0001t0003g0073a0002c0002t0005g0249 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.814+1097_814+1108d others(14): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465232
|
TTTGATTT others(9): Show |
T | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.814+1093_814+1108d others(18): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | ||||||
chr3:15465235
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(279): Show | 315 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(312): Show |
intron_variant | MODIFIER | c.814+1106C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465235 | ||||||
chr3:15465236
|
A | ATTTATTT others(52): Show |
1 | a0003c0004t0002g0022 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.814+1104_814+1105i others(61): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | ||||||
chr3:15465236
|
A | ATTTATTT others(48): Show |
1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.814+1104_814+1105i others(57): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | ||||||
chr3:15465236
|
A | T | 1 | a0001c0001t0002g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.814+1105T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | ||||||
chr3:15465284
|
T | A | 11 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0107others(8): Show | 13 | HG00558.hp1 HG00609.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+1057A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465284 | ||||||
chr3:15465330
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(190): Show | 220 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.814+1011C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465330 | ||||||
chr3:15465371
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.814+970C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465371 | ||||||
chr3:15465412
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.814+929C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465412 | ||||||
chr3:15465428
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+913C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465428 | ||||||
chr3:15465467
|
C | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+874G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465467 | ||||||
chr3:15465557
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+784G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465557 | ||||||
chr3:15465558
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.814+783C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465558 | ||||||
chr3:15465610
|
C | CT | 18 | a0001c0001t0001g0131a0001c0001t0001g0171a0001c0001t0001g0195others(15): Show | 20 | HG00280.hp2 HG01071.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.814+730dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | ||||||
chr3:15465610
|
C | CTT | 13 | a0001c0001t0001g0212a0001c0003t0004g0028a0001c0003t0004g0121others(10): Show | 14 | HG01109.hp2 HG02055.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.814+729_814+730dup others(2): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | ||||||
chr3:15465610
|
CTTT | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0260a0001c0001t0002g0297others(4): Show | 7 | HG01884.hp2 HG03041.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+728_814+730del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | ||||||
chr3:15465610
|
CTTTT | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(179): Show | 209 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.814+727_814+730del others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | ||||||
chr3:15465647
|
G | C | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.814+694C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465647 | ||||||
chr3:15465707
|
C | T | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.814+634G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465707 | ||||||
chr3:15465776
|
T | G | 9 | a0001c0001t0002g0343a0002c0002t0008g0269a0002c0002t0008g0270others(6): Show | 10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.814+565A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465776 | ||||||
chr3:15465794
|
G | A | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.814+547C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465794 | ||||||
chr3:15465815
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+526C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465815 | ||||||
chr3:15465901
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(176): Show | 205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.814+440G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465901 | ||||||
chr3:15465985
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0338others(1): Show | 4 | HG01168.hp1 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+356G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465985 | ||||||
chr3:15466108
|
T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.814+233A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15466108 | ||||||
chr3:15466254
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(176): Show | 205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.814+87C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15466254 | ||||||
chr3:15466613
|
A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.718-176T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466613 | ||||||
chr3:15466653
|
T | TCTGTC | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(207): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.718-217_718-216ins others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466653 | ||||||
chr3:15466745
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.718-308T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466745 | ||||||
chr3:15466802
|
G | C | 2 | a0001c0001t0010g0259a0001c0001t0016g0255 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.718-365C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466802 | ||||||
chr3:15466807
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.718-370G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466807 | ||||||
chr3:15466831
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.718-394G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466831 | ||||||
chr3:15466868
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.718-431T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466868 | ||||||
chr3:15466871
|
G | A | 9 | a0001c0001t0002g0343a0002c0002t0008g0269a0002c0002t0008g0270others(6): Show | 10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.718-434C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466871 | ||||||
chr3:15466888
|
C | T | 3 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266 | 3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.718-451G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466888 | ||||||
chr3:15466972
|
A | T | 3 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266 | 3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.718-535T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466972 | ||||||
chr3:15466992
|
A | C | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.718-555T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466992 | ||||||
chr3:15467054
|
C | T | 1 | a0001c0001t0003g0029 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.718-617G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467054 | ||||||
chr3:15467289
|
A | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718-852T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467289 | ||||||
chr3:15467511
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(206): Show | 237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-1074G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467511 | ||||||
chr3:15467521
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(206): Show | 237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-1084T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467521 | ||||||
chr3:15467561
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(11): Show | 20 | HG00639.hp1 HG01928.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.718-1124T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467561 | ||||||
chr3:15467616
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1179C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467616 | ||||||
chr3:15467705
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(207): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.718-1268A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467705 | ||||||
chr3:15467747
|
C | T | 4 | a0001c0001t0003g0010a0001c0001t0003g0037a0001c0001t0003g0052others(1): Show | 5 | NA18950.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1310G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467747 | ||||||
chr3:15467820
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(206): Show | 237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-1383G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467820 | ||||||
chr3:15468012
|
G | C | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.718-1575C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468012 | ||||||
chr3:15468321
|
G | GT | 14 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0001g0134others(11): Show | 14 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-1885dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468321
|
G | GTT | 57 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0100others(54): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.718-1886_718-1885d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468321
|
G | GTTT | 16 | a0001c0001t0001g0018a0001c0001t0001g0165a0001c0001t0001g0166others(13): Show | 17 | HG00735.hp1 HG01361.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-1887_718-1885d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468321
|
GT | G | 39 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0122others(36): Show | 40 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.718-1885delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468321
|
GTT | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(149): Show | 178 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.718-1886_718-1885d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468321
|
GTTT | G | 14 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0002g0307others(11): Show | 15 | HG01069.hp1 HG02129.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.718-1887_718-1885d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | ||||||
chr3:15468328
|
T | G | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1891A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468328 | ||||||
chr3:15468356
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.718-1919C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468356 | ||||||
chr3:15468384
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1947C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468384 | ||||||
chr3:15468399
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-1962G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468399 | ||||||
chr3:15468447
|
C | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(207): Show | 238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.718-2010G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468447 | ||||||
chr3:15468486
|
A | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.718-2049T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468486 | ||||||
chr3:15468626
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(206): Show | 237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.717+1910A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468626 | ||||||
chr3:15468770
|
T | C | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+1766A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468770 | ||||||
chr3:15468917
|
T | C | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.717+1619A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468917 | ||||||
chr3:15469012
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.717+1524G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469012 | ||||||
chr3:15469127
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.717+1409C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469127 | ||||||
chr3:15469260
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.717+1276A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469260 | ||||||
chr3:15469348
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.717+1188T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469348 | ||||||
chr3:15469348
|
A | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1188T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469348 | ||||||
chr3:15469373
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.717+1163A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469373 | ||||||
chr3:15469410
|
T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.717+1126A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469410 | ||||||
chr3:15469537
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(210): Show | 241 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.717+999T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469537 | ||||||
chr3:15469702
|
G | C | 6 | a0001c0001t0002g0245a0001c0001t0003g0029a0001c0001t0003g0039others(3): Show | 6 | HG00544.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+834C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469702 | ||||||
chr3:15469730
|
A | G | 17 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(14): Show | 18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.717+806T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469730 | ||||||
chr3:15469822
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0063a0001c0001t0003g0065 | 5 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+714C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469822 | ||||||
chr3:15470044
|
T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.717+492A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470044 | ||||||
chr3:15470323
|
A | C | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+213T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470323 | ||||||
chr3:15470508
|
G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.717+28C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470508 | ||||||
chr3:15470510
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.717+26G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470510 | ||||||
chr3:15470735
|
C | T | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-119G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470735 | ||||||
chr3:15470768
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.637-152T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470768 | ||||||
chr3:15470769
|
G | T | 26 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072others(23): Show | 27 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.637-153C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470769 | ||||||
chr3:15470787
|
A | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.637-171T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470787 | ||||||
chr3:15470859
|
A | G | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-243T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470859 | ||||||
chr3:15470953
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.637-337T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470953 | ||||||
chr3:15471072
|
G | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0165a0001c0001t0001g0166others(10): Show | 15 | HG02056.hp2 HG02071.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-456C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471072 | ||||||
chr3:15471161
|
A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-545T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471161 | ||||||
chr3:15471166
|
G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-550C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471166 | ||||||
chr3:15471169
|
T | C | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-553A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471169 | ||||||
chr3:15471256
|
A | G | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-640T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471256 | ||||||
chr3:15471292
|
A | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(169): Show | 197 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.637-676T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471292 | ||||||
chr3:15471304
|
T | C | 1 | a0001c0001t0003g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-688A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471304 | ||||||
chr3:15471541
|
T | C | 4 | a0001c0001t0007g0187a0001c0001t0007g0206a0001c0001t0007g0207others(1): Show | 4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-925A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471541 | ||||||
chr3:15471655
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637-1039C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471655 | ||||||
chr3:15471874
|
C | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.637-1258G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471874 | ||||||
chr3:15471875
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.637-1259C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471875 | ||||||
chr3:15471934
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.637-1318G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471934 | ||||||
chr3:15471946
|
G | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0006g0072 | 3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.637-1330C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471946 | ||||||
chr3:15471953
|
C | T | 1 | a0001c0001t0002g0023 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.637-1337G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471953 | ||||||
chr3:15471959
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(76): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.637-1343G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471959 | ||||||
chr3:15471969
|
A | AT | 7 | a0001c0001t0001g0188a0001c0001t0001g0274a0001c0001t0003g0042others(4): Show | 7 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-1354dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471969 | ||||||
chr3:15471969
|
AT | A | 52 | a0001c0001t0001g0181a0001c0001t0001g0218a0001c0001t0001g0248others(49): Show | 55 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.637-1354delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471969 | ||||||
chr3:15471970
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1354A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471970 | ||||||
chr3:15472067
|
A | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0326a0001c0001t0006g0051others(1): Show | 4 | HG00621.hp1 NA18945.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1451T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472067 | ||||||
chr3:15472068
|
G | T | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-1452C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472068 | ||||||
chr3:15472112
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.637-1496C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472112 | ||||||
chr3:15472137
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-1521G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472137 | ||||||
chr3:15472216
|
C | T | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-1600G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472216 | ||||||
chr3:15472246
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.637-1630A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472246 | ||||||
chr3:15472290
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.637-1674G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472290 | ||||||
chr3:15472447
|
A | G | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.636+1553T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472447 | ||||||
chr3:15472556
|
A | C | 19 | a0001c0001t0016g0255a0001c0003t0004g0028a0001c0003t0004g0121others(16): Show | 20 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.636+1444T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472556 | ||||||
chr3:15472722
|
G | A | 6 | a0001c0001t0002g0245a0001c0001t0003g0029a0001c0001t0003g0039others(3): Show | 6 | HG00544.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+1278C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472722 | ||||||
chr3:15472722
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.636+1278C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472722 | ||||||
chr3:15472790
|
T | A | 166 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(163): Show | 187 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.636+1210A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472790 | ||||||
chr3:15472850
|
CTTCTT | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0168a0001c0001t0010g0259 | 3 | HG03041.hp1 NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.636+1145_636+1149d others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472850 | ||||||
chr3:15472979
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+1021G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472979 | ||||||
chr3:15472987
|
G | T | 49 | a0001c0001t0002g0017a0001c0001t0002g0023a0001c0001t0002g0129others(46): Show | 60 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.636+1013C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472987 | ||||||
chr3:15473026
|
A | AT | 15 | a0001c0001t0002g0245a0001c0003t0004g0028a0001c0003t0004g0121others(12): Show | 16 | HG00544.hp2 HG01109.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.636+973dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473026 | ||||||
chr3:15473048
|
G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.636+952C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473048 | ||||||
chr3:15473058
|
T | C | 1 | a0001c0001t0001g0015 | 2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.636+942A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473058 | ||||||
chr3:15473264
|
G | A | 39 | a0001c0001t0002g0024a0001c0001t0002g0091a0001c0001t0002g0242others(36): Show | 44 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.636+736C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473264 | ||||||
chr3:15473299
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.636+701C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473299 | ||||||
chr3:15473554
|
C | T | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.636+446G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473554 | ||||||
chr3:15473595
|
T | G | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+405A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473595 | ||||||
chr3:15473648
|
G | A | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+352C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473648 | ||||||
chr3:15473741
|
A | C | 2 | a0001c0001t0002g0295a0001c0001t0013g0328 | 2 | HG02135.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.636+259T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473741 | ||||||
chr3:15474147
|
A | G | 1 | a0004c0006t0004g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.600+81T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474147 | ||||||
chr3:15474188
|
C | T | 182 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(179): Show | 204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.600+40G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474188 | ||||||
chr3:15474206
|
A | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.600+22T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474206 | ||||||
chr3:15474287
|
T | C | 11 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0013g0328others(8): Show | 12 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-15A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474287 | ||||||
chr3:15474411
|
C | G | 183 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(180): Show | 205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.556-139G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474411 | ||||||
chr3:15474434
|
A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.556-162T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474434 | ||||||
chr3:15474585
|
TGTG | T | 183 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(180): Show | 205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.556-316_556-314del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474585 | ||||||
chr3:15474671
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 6 | NA18944.hp2 NA18950.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+254G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474671 | ||||||
chr3:15474848
|
C | A | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.555+77G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474848 | ||||||
chr3:15474888
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555+37T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474888 | ||||||
chr3:15474889
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.555+36G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474889 | ||||||
chr3:15474974
|
T | C | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.529-23A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15474974 | ||||||
chr3:15475294
|
G | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0071a0001c0001t0006g0072 | 4 | HG02886.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+131C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475294 | ||||||
chr3:15475313
|
C | T | 153 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(150): Show | 173 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.528+112G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475313 | ||||||
chr3:15475403
|
T | C | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.528+22A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475403 | ||||||
chr3:15475518
|
G | A | 184 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(181): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.466-31C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475518 | ||||||
chr3:15475652
|
C | T | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.466-165G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475652 | ||||||
chr3:15475701
|
C | T | 7 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0005t0005g0264others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-214G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475701 | ||||||
chr3:15475811
|
C | G | 165 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(162): Show | 186 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.466-324G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475811 | ||||||
chr3:15475883
|
A | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.466-396T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475883 | ||||||
chr3:15475961
|
C | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.466-474G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475961 | ||||||
chr3:15475973
|
T | C | 54 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0026others(51): Show | 58 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.466-486A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475973 | ||||||
chr3:15476099
|
C | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.466-612G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476099 | ||||||
chr3:15476213
|
T | G | 1 | a0001c0001t0003g0078 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.466-726A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476213 | ||||||
chr3:15476234
|
A | G | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.466-747T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476234 | ||||||
chr3:15476283
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.466-796T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476283 | ||||||
chr3:15476402
|
C | T | 11 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0013g0328others(8): Show | 12 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+724G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476402 | ||||||
chr3:15476473
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+653A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476473 | ||||||
chr3:15476869
|
A | G | 18 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(15): Show | 19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.465+257T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476869 | ||||||
chr3:15477024
|
G | A | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+102C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477024 | ||||||
chr3:15477074
|
T | C | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+52A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477074 | ||||||
chr3:15477095
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0004c0006t0004g0244others(1): Show | 4 | HG01255.hp2 HG01346.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477095 | ||||||
chr3:15477224
|
G | C | 155 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(152): Show | 175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.394-27C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477224 | ||||||
chr3:15477231
|
G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394-34C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477231 | ||||||
chr3:15477334
|
G | A | 184 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(181): Show | 206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.394-137C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477334 | ||||||
chr3:15477382
|
T | C | 180 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(177): Show | 202 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.394-185A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477382 | ||||||
chr3:15477431
|
A | C | 1 | a0001c0001t0001g0338 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.394-234T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477431 | ||||||
chr3:15477584
|
C | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0322 | 3 | NA19063.hp1 NA19063.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.394-387G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477584 | ||||||
chr3:15477755
|
T | C | 159 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(156): Show | 180 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.394-558A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477755 | ||||||
chr3:15477850
|
G | A | 1 | a0001c0001t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.394-653C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477850 | ||||||
chr3:15478012
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(11): Show | 20 | HG00639.hp1 HG01928.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-815C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478012 | ||||||
chr3:15478144
|
T | A | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+833A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478144 | ||||||
chr3:15478190
|
GACC | G | 8 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(5): Show | 9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+784_393+786del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478190 | ||||||
chr3:15478270
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.393+707C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478270 | ||||||
chr3:15478350
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.393+627T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478350 | ||||||
chr3:15478427
|
C | T | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.393+550G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478427 | ||||||
chr3:15478453
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+524G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478453 | ||||||
chr3:15478512
|
G | T | 169 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(166): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.393+465C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478512 | ||||||
chr3:15478709
|
G | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.393+268C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478709 | ||||||
chr3:15478737
|
C | T | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.393+240G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478737 | ||||||
chr3:15478788
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.393+189A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478788 | ||||||
chr3:15478966
|
G | A | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+11C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478966 | ||||||
chr3:15479053
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG00733.hp1 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.367-50G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479053 | ||||||
chr3:15479132
|
T | G | 89 | a0001c0001t0002g0017a0001c0001t0002g0023a0001c0001t0002g0024others(86): Show | 105 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.367-129A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479132 | ||||||
chr3:15479143
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.367-140C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479143 | ||||||
chr3:15479170
|
G | T | 151 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(148): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.367-167C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479170 | ||||||
chr3:15479300
|
C | T | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.366+38G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479300 | ||||||
chr3:15479313
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.366+25C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479313 | ||||||
chr3:15479331
|
T | C | 11 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266others(8): Show | 12 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.366+7A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479331 | ||||||
chr3:15479556
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0013g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.322-174C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479556 | ||||||
chr3:15479629
|
G | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.322-247C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479629 | ||||||
chr3:15479989
|
A | G | 15 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0005t0005g0264others(12): Show | 16 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.322-607T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479989 | ||||||
chr3:15480112
|
C | T | 143 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0023others(140): Show | 163 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.322-730G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480112 | ||||||
chr3:15480158
|
G | A | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.322-776C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480158 | ||||||
chr3:15480214
|
G | A | 150 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(147): Show | 170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.322-832C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480214 | ||||||
chr3:15480338
|
C | A | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-956G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480338 | ||||||
chr3:15480392
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.322-1010A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480392 | ||||||
chr3:15480451
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-1069C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480451 | ||||||
chr3:15480462
|
C | G | 1 | a0001c0001t0001g0321 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.322-1080G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480462 | ||||||
chr3:15480597
|
T | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02486.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.322-1215A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480597 | ||||||
chr3:15480770
|
A | G | 154 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(151): Show | 175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.322-1388T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480770 | ||||||
chr3:15480866
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.322-1484A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480866 | ||||||
chr3:15481008
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-1626G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481008 | ||||||
chr3:15481429
|
T | C | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2047A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481429 | ||||||
chr3:15481696
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0016g0255 | 3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.322-2314C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481696 | ||||||
chr3:15481714
|
T | C | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322-2332A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481714 | ||||||
chr3:15481836
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.322-2454G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481836 | ||||||
chr3:15481857
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0308 | 2 | HG02056.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.322-2475A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481857 | ||||||
chr3:15481894
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.322-2512G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481894 | ||||||
chr3:15481932
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.322-2550G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481932 | ||||||
chr3:15481990
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.322-2608G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481990 | ||||||
chr3:15482086
|
T | C | 11 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266others(8): Show | 12 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.322-2704A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482086 | ||||||
chr3:15482180
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0260 | 2 | HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.322-2798G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482180 | ||||||
chr3:15482220
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.322-2838C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482220 | ||||||
chr3:15482225
|
C | T | 4 | a0001c0001t0002g0343a0001c0001t0010g0259a0004c0006t0004g0244others(1): Show | 4 | HG01884.hp2 HG03041.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-2843G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482225 | ||||||
chr3:15482369
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.322-2987A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482369 | ||||||
chr3:15482459
|
T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.322-3077A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482459 | ||||||
chr3:15482722
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(293): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.322-3340G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482722 | ||||||
chr3:15482745
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-3363G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482745 | ||||||
chr3:15482801
|
G | C | 1 | a0001c0001t0002g0161 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.322-3419C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482801 | ||||||
chr3:15482822
|
T | C | 4 | a0001c0001t0002g0343a0001c0001t0010g0259a0004c0006t0004g0244others(1): Show | 4 | HG01884.hp2 HG03041.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-3440A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482822 | ||||||
chr3:15482830
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.322-3448G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482830 | ||||||
chr3:15482847
|
T | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.322-3465A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482847 | ||||||
chr3:15482857
|
G | T | 4 | a0003c0004t0002g0022a0003c0004t0002g0256a0003c0004t0002g0257others(1): Show | 5 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-3475C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482857 | ||||||
chr3:15483079
|
C | A | 151 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(148): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.322-3697G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483079 | ||||||
chr3:15483126
|
G | A | 4 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0010g0342others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-3744C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483126 | ||||||
chr3:15483216
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322-3834C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483216 | ||||||
chr3:15483288
|
C | A | 14 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0311others(11): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-3906G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483288 | ||||||
chr3:15483518
|
T | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0120a0001c0001t0001g0177others(7): Show | 10 | NA18940.hp1 NA18942.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.322-4136A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483518 | ||||||
chr3:15483616
|
G | T | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.322-4234C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483616 | ||||||
chr3:15483662
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-4280A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483662 | ||||||
chr3:15483731
|
G | T | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.322-4349C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483731 | ||||||
chr3:15483819
|
A | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+4387T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483819 | ||||||
chr3:15484041
|
CT | C | 170 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(167): Show | 191 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.321+4164delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484041 | ||||||
chr3:15484158
|
C | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0016g0255 | 3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.321+4048G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484158 | ||||||
chr3:15484201
|
A | AG | 340 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(337): Show | 378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.321+4004_321+4005i others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484201 | ||||||
chr3:15484351
|
A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.321+3855T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484351 | ||||||
chr3:15484387
|
A | G | 169 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(166): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.321+3819T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484387 | ||||||
chr3:15484392
|
T | G | 18 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0002g0343others(15): Show | 19 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.321+3814A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484392 | ||||||
chr3:15484422
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.321+3784A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484422 | ||||||
chr3:15484523
|
T | A | 1 | a0001c0001t0002g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.321+3683A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484523 | ||||||
chr3:15484561
|
C | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+3645G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484561 | ||||||
chr3:15484563
|
T | C | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321+3643A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484563 | ||||||
chr3:15484586
|
C | T | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.321+3620G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484586 | ||||||
chr3:15484713
|
A | C | 1 | a0001c0001t0001g0277 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.321+3493T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484713 | ||||||
chr3:15484738
|
A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.321+3468T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484738 | ||||||
chr3:15484744
|
C | T | 3 | a0001c0001t0003g0080a0001c0001t0003g0082a0001c0001t0003g0083 | 3 | NA18948.hp2 NA18961.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.321+3462G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484744 | ||||||
chr3:15484771
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.321+3435A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484771 | ||||||
chr3:15484984
|
A | G | 5 | a0003c0004t0002g0022a0003c0004t0002g0247a0003c0004t0002g0256others(2): Show | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+3222T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484984 | ||||||
chr3:15485061
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.321+3145C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485061 | ||||||
chr3:15485234
|
G | T | 3 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266 | 3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+2972C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485234 | ||||||
chr3:15485295
|
G | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.321+2911C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485295 | ||||||
chr3:15485540
|
G | A | 185 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(182): Show | 207 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.321+2666C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485540 | ||||||
chr3:15485553
|
A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.321+2653T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485553 | ||||||
chr3:15485578
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.321+2628C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485578 | ||||||
chr3:15485701
|
T | C | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+2505A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485701 | ||||||
chr3:15485739
|
C | T | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+2467G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485739 | ||||||
chr3:15485742
|
G | C | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321+2464C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485742 | ||||||
chr3:15485938
|
G | C | 162 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(159): Show | 183 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.321+2268C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485938 | ||||||
chr3:15486164
|
T | A | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.321+2042A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486164 | ||||||
chr3:15486181
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.321+2025C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486181 | ||||||
chr3:15486272
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0125a0001c0001t0015g0116 | 4 | HG02258.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1934C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486272 | ||||||
chr3:15486366
|
T | G | 7 | a0001c0001t0002g0343a0001c0001t0010g0259a0001c0005t0005g0264others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1840A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486366 | ||||||
chr3:15486375
|
T | C | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+1831A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486375 | ||||||
chr3:15486407
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.321+1799G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486407 | ||||||
chr3:15486483
|
A | G | 9 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+1723T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486483 | ||||||
chr3:15486497
|
A | T | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.321+1709T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486497 | ||||||
chr3:15486555
|
T | C | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+1651A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486555 | ||||||
chr3:15486589
|
C | T | 1 | a0005c0009t0001g0344 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.321+1617G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486589 | ||||||
chr3:15486758
|
C | T | 3 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266 | 3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+1448G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486758 | ||||||
chr3:15486882
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.321+1324G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486882 | ||||||
chr3:15486992
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+1214G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486992 | ||||||
chr3:15487030
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0003g0062 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.321+1176C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487030 | ||||||
chr3:15487069
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(75): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.321+1137T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487069 | ||||||
chr3:15487255
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+951C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487255 | ||||||
chr3:15487324
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.321+882C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487324 | ||||||
chr3:15487383
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0016g0255 | 3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.321+823C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487383 | ||||||
chr3:15487425
|
C | T | 3 | a0001c0005t0005g0264a0001c0005t0005g0265a0002c0002t0005g0266 | 3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+781G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487425 | ||||||
chr3:15487546
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.321+660C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487546 | ||||||
chr3:15487558
|
C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.321+648G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487558 | ||||||
chr3:15487565
|
C | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+641G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487565 | ||||||
chr3:15487589
|
G | A | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+617C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487589 | ||||||
chr3:15487608
|
T | G | 21 | a0001c0001t0001g0115a0001c0001t0001g0131a0001c0001t0001g0132others(18): Show | 21 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+598A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487608 | ||||||
chr3:15487626
|
C | T | 2 | a0004c0006t0004g0244a0004c0006t0004g0246 | 2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+580G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487626 | ||||||
chr3:15487791
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.321+415C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487791 | ||||||
chr3:15487797
|
A | G | 155 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(152): Show | 176 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.321+409T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487797 | ||||||
chr3:15487898
|
C | A | 151 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(148): Show | 171 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.321+308G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487898 | ||||||
chr3:15487961
|
A | C | 1 | a0001c0001t0002g0280 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.321+245T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487961 | ||||||
chr3:15487998
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.321+208A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487998 | ||||||
chr3:15488036
|
T | C | 169 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(166): Show | 190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.321+170A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488036 | ||||||
chr3:15488175
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.321+31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488175 | ||||||
chr3:15488179
|
G | A | 4 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(1): Show | 4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+27C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488179 | ||||||
chr3:15488437
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG01891.hp1 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.220-130G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488437 | ||||||
chr3:15488440
|
C | G | 3 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0016g0255 | 3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.220-133G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488440 | ||||||
chr3:15488494
|
C | T | 15 | a0001c0003t0004g0028a0001c0003t0004g0121a0001c0003t0004g0272others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.220-187G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488494 | ||||||
chr3:15488512
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-205T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488512 | ||||||
chr3:15488552
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220-245C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488552 | ||||||
chr3:15488553
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220-246G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488553 | ||||||
chr3:15488598
|
A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.220-291T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488598 | ||||||
chr3:15488840
|
T | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0248others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-533A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488840 | ||||||
chr3:15489088
|
G | A | 153 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(150): Show | 172 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.219+437C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15489088 | ||||||
chr3:15489407
|
G | A | 1 | a0001c0003t0004g0337 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+118C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15489407 | ||||||
chr3:15489844
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.107-207T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15489844 | ||||||
chr3:15489909
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.107-272G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15489909 | ||||||
chr3:15490030
|
T | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.107-393A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490030 | ||||||
chr3:15490191
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107-554G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490191 | ||||||
chr3:15490210
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.107-573T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490210 | ||||||
chr3:15490330
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107-693C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490330 | ||||||
chr3:15490398
|
AT | A | 74 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(71): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.107-762delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490398 | ||||||
chr3:15490481
|
G | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-844C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490481 | ||||||
chr3:15490499
|
T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107-862A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490499 | ||||||
chr3:15490556
|
T | C | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107-919A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490556 | ||||||
chr3:15490760
|
C | T | 5 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-1123G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490760 | ||||||
chr3:15491020
|
TG | T | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-1384delC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491020 | ||||||
chr3:15491102
|
C | T | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-1465G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491102 | ||||||
chr3:15491160
|
A | G | 1 | a0001c0003t0004g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-1523T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491160 | ||||||
chr3:15491211
|
G | A | 12 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0010g0259others(9): Show | 14 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-1574C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491211 | ||||||
chr3:15491213
|
T | C | 4 | a0001c0001t0002g0242a0001c0001t0003g0062a0001c0001t0003g0074others(1): Show | 4 | HG01169.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1576A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491213 | ||||||
chr3:15491349
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG00733.hp1 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.107-1712G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491349 | ||||||
chr3:15491425
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0147 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107-1788C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491425 | ||||||
chr3:15491469
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-1832G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491469 | ||||||
chr3:15491639
|
C | T | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2002G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491639 | ||||||
chr3:15491726
|
A | G | 10 | a0001c0001t0001g0248a0001c0001t0001g0260a0002c0002t0005g0020others(7): Show | 12 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.107-2089T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491726 | ||||||
chr3:15491828
|
G | A | 5 | a0001c0001t0002g0245a0001c0001t0002g0343a0001c0003t0004g0272others(2): Show | 5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-2191C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491828 | ||||||
chr3:15491893
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107-2256T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491893 | ||||||
chr3:15491963
|
C | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-2326G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491963 | ||||||
chr3:15492056
|
C | CA | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(27): Show | 37 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-2420dupT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492056 | ||||||
chr3:15492056
|
CA | C | 43 | a0001c0001t0001g0274a0001c0001t0001g0308a0001c0001t0001g0310others(40): Show | 46 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.107-2420delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492056 | ||||||
chr3:15492121
|
C | T | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-2484G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492121 | ||||||
chr3:15492195
|
T | C | 5 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0001g0239others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-2558A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492195 | ||||||
chr3:15492533
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-2896C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492533 | ||||||
chr3:15492534
|
G | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-2897C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492534 | ||||||
chr3:15492591
|
C | T | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107-2954G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492591 | ||||||
chr3:15492666
|
CA | C | 175 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(172): Show | 197 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.107-3030delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492666 | ||||||
chr3:15492692
|
A | G | 75 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.107-3055T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492692 | ||||||
chr3:15492847
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.107-3210G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492847 | ||||||
chr3:15492925
|
TG | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0063 | 4 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-3289delC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492925 | ||||||
chr3:15493210
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-3573C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493210 | ||||||
chr3:15493246
|
G | A | 5 | a0001c0001t0002g0245a0001c0001t0002g0343a0001c0003t0004g0272others(2): Show | 5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-3609C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493246 | ||||||
chr3:15493268
|
C | T | 2 | a0001c0001t0010g0259a0001c0001t0016g0255 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.107-3631G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493268 | ||||||
chr3:15493288
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107-3651T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493288 | ||||||
chr3:15493366
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107-3729G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493366 | ||||||
chr3:15493400
|
T | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-3763A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493400 | ||||||
chr3:15493526
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-3889G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493526 | ||||||
chr3:15493675
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-4038G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493675 | ||||||
chr3:15493680
|
G | A | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-4043C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493680 | ||||||
chr3:15493693
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.107-4056G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493693 | ||||||
chr3:15493694
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-4057G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493694 | ||||||
chr3:15493809
|
C | T | 2 | a0001c0001t0001g0236a0001c0008t0001g0190 | 2 | NA18612.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.107-4172G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493809 | ||||||
chr3:15493904
|
G | A | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-4267C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493904 | ||||||
chr3:15493944
|
G | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-4307C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493944 | ||||||
chr3:15494198
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.107-4561C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494198 | ||||||
chr3:15494314
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-4677G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494314 | ||||||
chr3:15494315
|
G | A | 5 | a0001c0001t0002g0245a0001c0001t0002g0343a0001c0003t0004g0272others(2): Show | 5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4678C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494315 | ||||||
chr3:15494347
|
C | T | 5 | a0001c0001t0002g0245a0001c0001t0002g0343a0001c0003t0004g0272others(2): Show | 5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4710G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494347 | ||||||
chr3:15494403
|
G | A | 53 | a0001c0001t0001g0274a0001c0001t0001g0308a0001c0001t0001g0310others(50): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-4766C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494403 | ||||||
chr3:15494412
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-4775A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494412 | ||||||
chr3:15494513
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-4876C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494513 | ||||||
chr3:15494519
|
G | C | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-4882C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494519 | ||||||
chr3:15494536
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.107-4899C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494536 | ||||||
chr3:15494556
|
A | G | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-4919T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494556 | ||||||
chr3:15494565
|
T | C | 74 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(71): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.107-4928A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494565 | ||||||
chr3:15494567
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.107-4930C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494567 | ||||||
chr3:15494814
|
A | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-5177T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494814 | ||||||
chr3:15495127
|
G | A | 76 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0242others(73): Show | 90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-5490C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495127 | ||||||
chr3:15495199
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(21): Show | 30 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.107-5562C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495199 | ||||||
chr3:15495326
|
G | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(205): Show | 236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.107-5689C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495326 | ||||||
chr3:15495391
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107-5754G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495391 | ||||||
chr3:15495504
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.107-5867A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495504 | ||||||
chr3:15495622
|
A | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-5985T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495622 | ||||||
chr3:15495733
|
G | T | 1 | a0001c0001t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.107-6096C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495733 | ||||||
chr3:15495746
|
C | A | 2 | a0001c0001t0002g0016a0001c0001t0015g0116 | 3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.107-6109G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495746 | ||||||
chr3:15496010
|
A | G | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.107-6373T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496010 | ||||||
chr3:15496188
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0003g0063a0001c0001t0003g0065others(1): Show | 6 | NA18612.hp1 NA18945.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-6551G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496188 | ||||||
chr3:15496217
|
T | A | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.107-6580A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496217 | ||||||
chr3:15496218
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.107-6581G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496218 | ||||||
chr3:15496269
|
A | G | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6632T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496269 | ||||||
chr3:15496411
|
A | G | 6 | a0001c0001t0001g0118a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-6774T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496411 | ||||||
chr3:15496484
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-6847A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496484 | ||||||
chr3:15496485
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(151): Show | 179 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.107-6848T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496485 | ||||||
chr3:15496486
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.107-6849A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496486 | ||||||
chr3:15496665
|
C | T | 5 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(2): Show | 6 | HG02970.hp2 HG02976.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-7028G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496665 | ||||||
chr3:15496733
|
A | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-7096T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496733 | ||||||
chr3:15496951
|
A | G | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-7314T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496951 | ||||||
chr3:15496970
|
T | C | 71 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(68): Show | 77 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.107-7333A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496970 | ||||||
chr3:15497034
|
GC | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0049 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.107-7398delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497034 | ||||||
chr3:15497036
|
C | CT | 49 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(46): Show | 56 | HG00639.hp1 HG00673.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-7400dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497036
|
C | CTT | 7 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0099others(4): Show | 7 | HG01168.hp1 HG02055.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-7401_107-7400d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497036
|
C | CTTT | 14 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0002g0245others(11): Show | 15 | HG00544.hp2 HG01081.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-7402_107-7400d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497036
|
CT | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0213a0001c0001t0001g0232others(3): Show | 6 | HG01943.hp2 HG01993.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-7400delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497036
|
CTTTTTTT | C | 12 | a0001c0001t0001g0248a0001c0001t0001g0260a0002c0002t0005g0020others(9): Show | 14 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-7406_107-7400d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497036
|
CTTTTTTT others(1): Show |
C | 58 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(55): Show | 62 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.107-7407_107-7400d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | ||||||
chr3:15497132
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.107-7495G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497132 | ||||||
chr3:15497172
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.107-7535G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497172 | ||||||
chr3:15497207
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.107-7570G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497207 | ||||||
chr3:15497263
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-7626A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497263 | ||||||
chr3:15497518
|
G | A | 1 | a0001c0001t0002g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-7881C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497518 | ||||||
chr3:15497739
|
C | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0029a0001c0001t0003g0039others(7): Show | 11 | HG00558.hp2 HG00609.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-8102G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497739 | ||||||
chr3:15498186
|
G | A | 5 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271others(2): Show | 6 | HG02970.hp2 HG02976.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-8549C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498186 | ||||||
chr3:15498263
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(333): Show | 374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.107-8626A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498263 | ||||||
chr3:15498469
|
C | CCA | 5 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(2): Show | 5 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-8834_107-8833d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | ||||||
chr3:15498469
|
C | CCACA | 77 | a0001c0001t0001g0274a0001c0001t0002g0024a0001c0001t0002g0242others(74): Show | 91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.107-8836_107-8833d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | ||||||
chr3:15498469
|
C | CCACACA | 86 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(83): Show | 92 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-8838_107-8833d others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | ||||||
chr3:15498469
|
C | CCACACAC others(1): Show |
34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(31): Show | 42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-8840_107-8833d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | ||||||
chr3:15498496
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.107-8859G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498496 | ||||||
chr3:15498641
|
T | G | 76 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(73): Show | 90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-9004A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498641 | ||||||
chr3:15498649
|
G | A | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-9012C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498649 | ||||||
chr3:15498930
|
A | ATCAG | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9294_107-9293i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498930 | ||||||
chr3:15498966
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9329T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498966 | ||||||
chr3:15499026
|
C | A | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-9389G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499026 | ||||||
chr3:15499334
|
T | C | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-9697A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499334 | ||||||
chr3:15499530
|
T | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9893A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499530 | ||||||
chr3:15499555
|
A | G | 53 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0308others(50): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-9918T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499555 | ||||||
chr3:15499609
|
T | C | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.107-9972A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499609 | ||||||
chr3:15499707
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(98): Show | 121 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.107-10070A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499707 | ||||||
chr3:15499743
|
C | G | 1 | a0001c0001t0001g0321 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.107-10106G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499743 | ||||||
chr3:15499822
|
G | A | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-10185C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499822 | ||||||
chr3:15500334
|
T | C | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-10697A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500334 | ||||||
chr3:15500334
|
T | G | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-10697A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500334 | ||||||
chr3:15500483
|
T | C | 2 | a0003c0004t0002g0257a0003c0004t0002g0258 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.107-10846A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500483 | ||||||
chr3:15500624
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.107-10987C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500624 | ||||||
chr3:15500783
|
C | T | 94 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(91): Show | 102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.107-11146G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500783 | ||||||
chr3:15500883
|
C | A | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | NA18952.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.107-11246G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500883 | ||||||
chr3:15500905
|
T | C | 14 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0010g0259others(11): Show | 17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-11268A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500905 | ||||||
chr3:15501155
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.107-11518T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501155 | ||||||
chr3:15501220
|
A | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.107-11583T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501220 | ||||||
chr3:15501250
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.107-11613C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501250 | ||||||
chr3:15501253
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.107-11616G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501253 | ||||||
chr3:15501266
|
C | T | 97 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(94): Show | 105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.107-11629G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501266 | ||||||
chr3:15501335
|
G | A | 1 | a0001c0001t0006g0059 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.107-11698C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501335 | ||||||
chr3:15501629
|
G | A | 89 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(86): Show | 97 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-11992C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501629 | ||||||
chr3:15501655
|
G | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107-12018C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501655 | ||||||
chr3:15501685
|
C | T | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-12048G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501685 | ||||||
chr3:15502113
|
A | AT | 97 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(94): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.107-12477dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | ||||||
chr3:15502113
|
AT | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(96): Show | 112 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.107-12477delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | ||||||
chr3:15502113
|
ATTT | A | 73 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(70): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.107-12479_107-1247 others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | ||||||
chr3:15502167
|
GTGCAATG others(17): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107-12554_107-1253 others(28): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502167 | ||||||
chr3:15502208
|
C | T | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-12571G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502208 | ||||||
chr3:15502240
|
G | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(199): Show | 230 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.107-12603C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502240 | ||||||
chr3:15502296
|
T | C | 2 | a0002c0002t0005g0253a0002c0002t0005g0254 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.107-12659A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502296 | ||||||
chr3:15502331
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107-12694C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502331 | ||||||
chr3:15502439
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(98): Show | 121 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.107-12802T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502439 | ||||||
chr3:15502836
|
T | C | 51 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0308others(48): Show | 54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.107-13199A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502836 | ||||||
chr3:15503022
|
G | A | 72 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(69): Show | 79 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.107-13385C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503022 | ||||||
chr3:15503031
|
C | A | 1 | a0001c0001t0003g0078 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.107-13394G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503031 | ||||||
chr3:15503040
|
C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107-13403G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503040 | ||||||
chr3:15503121
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-13484G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503121 | ||||||
chr3:15503148
|
T | C | 1 | a0001c0003t0004g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107-13511A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503148 | ||||||
chr3:15503246
|
A | G | 1 | a0001c0003t0004g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-13609T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503246 | ||||||
chr3:15503261
|
C | T | 4 | a0001c0001t0010g0259a0001c0001t0016g0255a0003c0004t0002g0022others(1): Show | 5 | HG03041.hp1 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-13624G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503261 | ||||||
chr3:15503288
|
C | T | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-13651G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503288 | ||||||
chr3:15503310
|
GC | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0287 | 3 | HG00544.hp1 NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.107-13674delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503310 | ||||||
chr3:15503410
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.107-13773A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503410 | ||||||
chr3:15503423
|
G | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-13786C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503423 | ||||||
chr3:15503484
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-13847G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503484 | ||||||
chr3:15503598
|
C | T | 89 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(86): Show | 97 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-13961G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503598 | ||||||
chr3:15503703
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0148a0001c0001t0001g0170others(7): Show | 11 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-14066G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503703 | ||||||
chr3:15503755
|
G | A | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-14118C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503755 | ||||||
chr3:15503803
|
A | C | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-14166T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503803 | ||||||
chr3:15503968
|
C | G | 76 | a0001c0001t0002g0024a0001c0001t0002g0242a0001c0001t0002g0267others(73): Show | 90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-14331G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503968 | ||||||
chr3:15504147
|
T | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-14510A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504147 | ||||||
chr3:15504212
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.107-14575C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504212 | ||||||
chr3:15504230
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.107-14593G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504230 | ||||||
chr3:15504349
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-14712G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504349 | ||||||
chr3:15504363
|
C | G | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-14726G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504363 | ||||||
chr3:15504391
|
T | C | 14 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0010g0259others(11): Show | 17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-14754A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504391 | ||||||
chr3:15504456
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107-14819C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504456 | ||||||
chr3:15504568
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.107-14931A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504568 | ||||||
chr3:15504596
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(195): Show | 226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-14959A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504596 | ||||||
chr3:15504639
|
A | T | 29 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(26): Show | 32 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.107-15002T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504639 | ||||||
chr3:15504841
|
T | C | 5 | a0001c0001t0002g0245a0001c0001t0002g0343a0001c0003t0004g0272others(2): Show | 5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-15204A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504841 | ||||||
chr3:15505061
|
A | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0002g0023others(2): Show | 6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-15424T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505061 | ||||||
chr3:15505135
|
C | T | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-15498G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505135 | ||||||
chr3:15505334
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.107-15697G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505334 | ||||||
chr3:15505361
|
G | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.107-15724C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505361 | ||||||
chr3:15505363
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(191): Show | 222 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.107-15726C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505363 | ||||||
chr3:15505642
|
C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+15878G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505642 | ||||||
chr3:15505694
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.106+15826G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505694 | ||||||
chr3:15505738
|
C | CA | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+15781dupT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505738 | ||||||
chr3:15505803
|
C | T | 94 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(91): Show | 102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.106+15717G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505803 | ||||||
chr3:15506100
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.106+15420C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506100 | ||||||
chr3:15506254
|
T | G | 51 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0308others(48): Show | 54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.106+15266A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506254 | ||||||
chr3:15506357
|
T | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+15163A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506357 | ||||||
chr3:15506389
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+15131G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506389 | ||||||
chr3:15506463
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+15057G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506463 | ||||||
chr3:15506480
|
A | T | 5 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+15040T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506480 | ||||||
chr3:15506584
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0014others(1): Show | 6 | HG01099.hp1 HG01934.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+14936A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506584 | ||||||
chr3:15506624
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+14896T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506624 | ||||||
chr3:15506652
|
C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+14868G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506652 | ||||||
chr3:15506720
|
G | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+14800C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506720 | ||||||
chr3:15506721
|
C | A | 1 | a0001c0003t0004g0340 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+14799G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506721 | ||||||
chr3:15506734
|
C | T | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0129others(2): Show | 5 | HG01256.hp1 HG02300.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+14786G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506734 | ||||||
chr3:15506944
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 123 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.106+14576A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506944 | ||||||
chr3:15507079
|
C | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+14441G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507079 | ||||||
chr3:15507091
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 10 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+14429C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507091 | ||||||
chr3:15507267
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.106+14253G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507267 | ||||||
chr3:15507375
|
G | A | 4 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(1): Show | 4 | NA18987.hp1 NA19009.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+14145C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507375 | ||||||
chr3:15507550
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01891.hp2 HG02647.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+13970C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507550 | ||||||
chr3:15507684
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.106+13836C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507684 | ||||||
chr3:15507695
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.106+13825A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507695 | ||||||
chr3:15507834
|
C | T | 12 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(9): Show | 13 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+13686G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507834 | ||||||
chr3:15507886
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+13634G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507886 | ||||||
chr3:15507937
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.106+13583T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507937 | ||||||
chr3:15508019
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106+13501G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508019 | ||||||
chr3:15508020
|
G | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+13500C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508020 | ||||||
chr3:15508169
|
C | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+13351G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508169 | ||||||
chr3:15508356
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.106+13164A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508356 | ||||||
chr3:15508398
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+13122C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508398 | ||||||
chr3:15508460
|
A | C | 5 | a0001c0001t0001g0237a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+13060T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508460 | ||||||
chr3:15508496
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106+13024T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508496 | ||||||
chr3:15508715
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+12805A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508715 | ||||||
chr3:15508725
|
G | C | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106+12795C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508725 | ||||||
chr3:15508865
|
T | C | 3 | a0003c0004t0002g0247a0003c0004t0002g0257a0003c0004t0002g0258 | 3 | HG02622.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.106+12655A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508865 | ||||||
chr3:15508872
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+12648G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508872 | ||||||
chr3:15509060
|
A | G | 1 | a0001c0001t0003g0037 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.106+12460T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509060 | ||||||
chr3:15509103
|
C | T | 74 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(71): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.106+12417G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509103 | ||||||
chr3:15509127
|
T | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+12393A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509127 | ||||||
chr3:15509133
|
G | A | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+12387C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509133 | ||||||
chr3:15509184
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.106+12336T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509184 | ||||||
chr3:15509190
|
A | C | 84 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(81): Show | 90 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.106+12330T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509190 | ||||||
chr3:15509232
|
GGCCTGGT others(15): Show |
G | 1 | a0001c0001t0003g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106+12266_106+1228 others(26): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509232 | ||||||
chr3:15509572
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+11948G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509572 | ||||||
chr3:15509673
|
T | C | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+11847A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509673 | ||||||
chr3:15509703
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.106+11817T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509703 | ||||||
chr3:15509708
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+11812G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509708 | ||||||
chr3:15509764
|
G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0234 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.106+11756C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509764 | ||||||
chr3:15509792
|
T | C | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+11728A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509792 | ||||||
chr3:15509799
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.106+11721A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509799 | ||||||
chr3:15509912
|
C | T | 2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.106+11608G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509912 | ||||||
chr3:15510037
|
G | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11483C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510037 | ||||||
chr3:15510045
|
G | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11475C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510045 | ||||||
chr3:15510093
|
G | A | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106+11427C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510093 | ||||||
chr3:15510099
|
C | G | 2 | a0003c0004t0002g0257a0003c0004t0002g0258 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+11421G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510099 | ||||||
chr3:15510181
|
A | C | 3 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036 | 3 | HG01981.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.106+11339T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510181 | ||||||
chr3:15510332
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+11188A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510332 | ||||||
chr3:15510407
|
A | G | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+11113T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510407 | ||||||
chr3:15510414
|
G | T | 1 | a0001c0001t0003g0033 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.106+11106C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510414 | ||||||
chr3:15510484
|
G | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11036C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510484 | ||||||
chr3:15510490
|
C | CT | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+11029dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510490 | ||||||
chr3:15510550
|
A | C | 7 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(4): Show | 7 | NA18944.hp1 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+10970T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510550 | ||||||
chr3:15510563
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+10957G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510563 | ||||||
chr3:15510641
|
G | A | 1 | a0001c0001t0002g0317 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.106+10879C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510641 | ||||||
chr3:15510708
|
AAGGGGAC others(8): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.106+10797_106+1081 others(19): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510708 | ||||||
chr3:15510752
|
G | T | 94 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(91): Show | 102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.106+10768C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510752 | ||||||
chr3:15510808
|
C | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(191): Show | 222 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.106+10712G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510808 | ||||||
chr3:15510858
|
A | AGAAG | 42 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(39): Show | 49 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.106+10658_106+1066 others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | ||||||
chr3:15510858
|
A | AGAAGGAA others(13): Show |
3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+10642_106+1066 others(24): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | ||||||
chr3:15510858
|
AGAAG | A | 72 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(69): Show | 79 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.106+10658_106+1066 others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | ||||||
chr3:15510858
|
AGAAGGAA others(1): Show |
A | 3 | a0002c0002t0008g0269a0002c0002t0008g0270a0002c0002t0008g0271 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+10654_106+1066 others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | ||||||
chr3:15511072
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.106+10448A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511072 | ||||||
chr3:15511244
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+10276G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511244 | ||||||
chr3:15511277
|
G | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+10243C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511277 | ||||||
chr3:15511641
|
G | T | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0010g0342others(1): Show | 4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+9879C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511641 | ||||||
chr3:15511719
|
A | C | 1 | a0001c0001t0002g0023 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.106+9801T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511719 | ||||||
chr3:15511749
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 228 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.106+9771G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511749 | ||||||
chr3:15511814
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.106+9706G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511814 | ||||||
chr3:15512082
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+9438A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512082 | ||||||
chr3:15512170
|
G | C | 98 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0001g0262others(95): Show | 106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.106+9350C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512170 | ||||||
chr3:15512230
|
G | A | 9 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0002g0245others(6): Show | 9 | HG00544.hp2 HG01081.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9290C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512230 | ||||||
chr3:15512242
|
T | G | 2 | a0001c0001t0001g0144a0005c0009t0001g0344 | 2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.106+9278A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512242 | ||||||
chr3:15512274
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(97): Show | 120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+9246C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512274 | ||||||
chr3:15512309
|
C | T | 2 | a0001c0001t0010g0342a0001c0001t0013g0328 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.106+9211G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512309 | ||||||
chr3:15512487
|
C | G | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+9033G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512487 | ||||||
chr3:15512505
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.106+9015C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512505 | ||||||
chr3:15512726
|
T | C | 53 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0308others(50): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.106+8794A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512726 | ||||||
chr3:15512800
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.106+8720G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512800 | ||||||
chr3:15512949
|
C | A | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+8571G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512949 | ||||||
chr3:15512957
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.106+8563G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512957 | ||||||
chr3:15513119
|
T | C | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+8401A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513119 | ||||||
chr3:15513119
|
T | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+8401A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513119 | ||||||
chr3:15513372
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.106+8148G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513372 | ||||||
chr3:15513492
|
A | G | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+8028T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513492 | ||||||
chr3:15513763
|
G | A | 51 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0308others(48): Show | 54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.106+7757C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513763 | ||||||
chr3:15513915
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+7605G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513915 | ||||||
chr3:15513941
|
A | C | 1 | a0001c0003t0004g0331 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106+7579T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513941 | ||||||
chr3:15514141
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.106+7379C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514141 | ||||||
chr3:15514525
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.106+6995G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514525 | ||||||
chr3:15514756
|
G | A | 1 | a0001c0001t0003g0079 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.106+6764C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514756 | ||||||
chr3:15514795
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+6725C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514795 | ||||||
chr3:15514900
|
T | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.106+6620A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514900 | ||||||
chr3:15514935
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+6585G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514935 | ||||||
chr3:15515087
|
T | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0030a0001c0001t0003g0080others(8): Show | 13 | HG01433.hp2 HG01928.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+6433A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515087 | ||||||
chr3:15515120
|
T | C | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+6400A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515120 | ||||||
chr3:15515611
|
C | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+5909G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515611 | ||||||
chr3:15515636
|
C | T | 74 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(71): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.106+5884G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515636 | ||||||
chr3:15515667
|
G | T | 1 | a0001c0001t0003g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.106+5853C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515667 | ||||||
chr3:15515800
|
C | T | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+5720G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515800 | ||||||
chr3:15515883
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(23): Show | 32 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.106+5637C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515883 | ||||||
chr3:15516033
|
C | T | 14 | a0001c0001t0001g0338a0001c0003t0004g0028a0001c0003t0004g0121others(11): Show | 15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+5487G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516033 | ||||||
chr3:15516078
|
C | A | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | NA18952.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.106+5442G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516078 | ||||||
chr3:15516088
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.106+5432A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516088 | ||||||
chr3:15516175
|
T | A | 17 | a0001c0001t0001g0237a0001c0001t0002g0017a0001c0001t0002g0149others(14): Show | 18 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+5345A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516175 | ||||||
chr3:15516365
|
A | G | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+5155T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516365 | ||||||
chr3:15516662
|
C | T | 58 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0274others(55): Show | 62 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.106+4858G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516662 | ||||||
chr3:15516704
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+4816G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516704 | ||||||
chr3:15516906
|
T | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+4614A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516906 | ||||||
chr3:15517057
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106+4463C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517057 | ||||||
chr3:15517143
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+4377C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517143 | ||||||
chr3:15517144
|
A | T | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+4376T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517144 | ||||||
chr3:15517160
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.106+4360T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517160 | ||||||
chr3:15517445
|
G | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+4075C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517445 | ||||||
chr3:15517567
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+3953A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517567 | ||||||
chr3:15517640
|
C | A | 2 | a0001c0001t0002g0016a0001c0001t0015g0116 | 3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.106+3880G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517640 | ||||||
chr3:15517662
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(105): Show | 128 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.106+3858A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517662 | ||||||
chr3:15517667
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106+3853A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517667 | ||||||
chr3:15517721
|
C | T | 16 | a0001c0001t0002g0017a0001c0001t0002g0149a0001c0001t0002g0150others(13): Show | 17 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+3799G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517721 | ||||||
chr3:15517827
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0015g0116 | 3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.106+3693G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517827 | ||||||
chr3:15517891
|
C | T | 1 | a0001c0001t0003g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.106+3629G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517891 | ||||||
chr3:15517894
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.106+3626G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517894 | ||||||
chr3:15518642
|
T | C | 7 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0002g0023others(4): Show | 8 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2878A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518642 | ||||||
chr3:15518736
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.106+2784G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518736 | ||||||
chr3:15518829
|
T | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(194): Show | 225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+2691A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518829 | ||||||
chr3:15518861
|
T | G | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+2659A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518861 | ||||||
chr3:15519040
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0147 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.106+2480A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519040 | ||||||
chr3:15519158
|
AC | A | 75 | a0001c0001t0002g0024a0001c0001t0002g0267a0001c0001t0003g0003others(72): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+2361delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519158 | ||||||
chr3:15519208
|
T | G | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+2312A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519208 | ||||||
chr3:15519450
|
C | T | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+2070G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519450 | ||||||
chr3:15519559
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.106+1961A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519559 | ||||||
chr3:15519676
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.106+1844C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519676 | ||||||
chr3:15519751
|
G | T | 3 | a0001c0001t0002g0245a0004c0006t0004g0244a0004c0006t0004g0246 | 3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+1769C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519751 | ||||||
chr3:15519840
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0003t0004g0123 | 3 | HG02109.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.106+1680T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519840 | ||||||
chr3:15519983
|
T | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(29): Show | 38 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.106+1537A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519983 | ||||||
chr3:15519985
|
G | A | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+1535C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519985 | ||||||
chr3:15520063
|
TTCCTTAA others(4): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.106+1446_106+1456d others(13): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520063 | ||||||
chr3:15520104
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(198): Show | 229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+1416T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520104 | ||||||
chr3:15520172
|
G | T | 1 | a0001c0001t0002g0278 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.106+1348C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520172 | ||||||
chr3:15520390
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106+1130G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520390 | ||||||
chr3:15520557
|
C | G | 3 | a0001c0001t0001g0277a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG00733.hp2 HG01943.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.106+963G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520557 | ||||||
chr3:15520634
|
G | A | 49 | a0001c0001t0001g0277a0001c0001t0001g0308a0001c0001t0001g0310others(46): Show | 52 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.106+886C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520634 | ||||||
chr3:15520731
|
G | A | 2 | a0001c0001t0002g0343a0001c0003t0004g0272 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+789C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520731 | ||||||
chr3:15520739
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(180): Show | 208 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.106+781T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520739 | ||||||
chr3:15521004
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.106+516C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521004 | ||||||
chr3:15521011
|
A | AC | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG01109.hp2 HG02004.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+508dupG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521011 | ||||||
chr3:15521017
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.106+503G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521017 | ||||||
chr3:15521199
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0092others(194): Show | 223 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.106+321T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521199 | ||||||
chr3:15521247
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.106+273T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521247 | ||||||
chr3:15521281
|
C | A | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0338others(15): Show | 19 | HG01081.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+239G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521281 | ||||||
chr3:15521294
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(202): Show | 233 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.106+226A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521294 | ||||||
chr3:15521324
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(22): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+196G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521324 |