geneid | 1047 |
---|---|
ensemblid | ENSG00000153132.13 |
hgncid | 2060 |
symbol | CLGN |
name | calmegin |
refseq_nuc | NM_004362.3 |
refseq_prot | NP_004353.1 |
ensembl_nuc | ENST00000325617.10 |
ensembl_prot | ENSP00000326699.5 |
mane_status | MANE Select |
chr | chr4 |
start | 140388453 |
end | 140427648 |
strand | - |
ver | v1.2 |
region | chr4:140388453-140427648 |
region5000 | chr4:140383453-140432648 |
regionname0 | CLGN_chr4_140388453_140427648 |
regionname5000 | CLGN_chr4_140383453_140432648 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 610 | 278 | 75 | 56 | 107 | 9 | 30 | 85 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0002 | 0/0 | 610 | 57 | 4 | 12 | 34 | 1 | 6 | 26 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0003 | 0/1 | 610 | 14 | 11 | 1 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0004 | 0/0 | 610 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0005 | 0/0 | 610 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0006 | 0/0 | 607 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0007 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1833 | 272 | 71 | 54 | 107 | 9 | 30 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0002 | 0/0 | 1833 | 52 | 4 | 10 | 34 | 1 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0003 | 0/1 | 1833 | 14 | 11 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0004 | 0/0 | 1833 | 5 | 0 | 2 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0005 | 0/0 | 1833 | 4 | 0 | 3 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0006 | 0/0 | 1833 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0007 | 0/0 | 1833 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0008 | 0/0 | 1833 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0009 | 0/0 | 1833 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0010 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
c0011 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 893 | 272 | 73 | 56 | 98 | 9 | 35 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0002 | 0/0 | 893 | 64 | 3 | 15 | 41 | 3 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0003 | 0/1 | 893 | 9 | 7 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0004 | 0/0 | 893 | 6 | 6 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0005 | 0/0 | 893 | 3 | 0 | 0 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0006 | 0/0 | 893 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0007 | 0/0 | 893 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
t0008 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 2 | 5 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0003 | 0/0 | 7 | 2 | 5 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1833 | 272 | 71 | 54 | 107 | 9 | 30 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0006 | 0/0 | 1833 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0007 | 0/0 | 1833 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0010 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0002c0002 | 0/0 | 1833 | 52 | 4 | 10 | 34 | 1 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0002c0004 | 0/0 | 1833 | 5 | 0 | 2 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0003c0003 | 0/1 | 1833 | 14 | 11 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0004c0005 | 0/0 | 1833 | 4 | 0 | 3 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0005c0008 | 0/0 | 1833 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0006c0009 | 0/0 | 1833 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0007c0011 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2725 | 199 | 65 | 39 | 63 | 6 | 25 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0002 | 0/0 | 2725 | 64 | 3 | 15 | 41 | 3 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0004 | 0/0 | 2725 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0005 | 0/0 | 2725 | 3 | 0 | 0 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0006 | 0/0 | 2725 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0007 | 0/0 | 2725 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0001t0008 | 0/0 | 2725 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0006t0001 | 0/0 | 2725 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0007t0001 | 0/0 | 2725 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0001c0010t0001 | 0/0 | 2725 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0002c0002t0001 | 0/0 | 2725 | 52 | 4 | 10 | 34 | 1 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0002c0004t0001 | 0/0 | 2725 | 5 | 0 | 2 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0003c0003t0001 | 0/0 | 2725 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0003c0003t0003 | 0/1 | 2725 | 9 | 7 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0003c0003t0004 | 0/0 | 2725 | 4 | 4 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0004c0005t0001 | 0/0 | 2725 | 4 | 0 | 3 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0005c0008t0001 | 0/0 | 2725 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0006c0009t0001 | 0/0 | 2725 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
a0007c0011t0001 | 0/0 | 2725 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | copy fasta | chr4 | 140383453 | 140432648 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 5 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0003 | 0/0 | 7 | 2 | 5 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0007t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0001c0010t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0002c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0003c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0004c0005t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0004c0005t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0005c0008t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0006c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0006c0009t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
a0007c0011t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0208 | EUR | GBR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00642 | hp2 | a0002 | c0004 | t0001 | g0227 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00738 | hp2 | a0004 | c0005 | t0001 | g0026 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0260 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01106 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01168 | hp1 | a0004 | c0005 | t0001 | g0025 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01169 | hp1 | a0004 | c0005 | t0001 | g0025 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0029 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01258 | hp2 | a0001 | c0007 | t0001 | g0029 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0245 | EUR | IBS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02165 | hp2 | a0001 | c0001 | t0008 | g0069 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0037 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02717 | hp2 | a0003 | c0003 | t0003 | g0247 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02896 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02897 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03139 | hp1 | a0001 | c0006 | t0001 | g0211 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03195 | hp2 | a0003 | c0003 | t0003 | g0007 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03490 | hp1 | a0002 | c0004 | t0001 | g0127 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03491 | hp2 | a0005 | c0008 | t0001 | g0034 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03492 | hp1 | a0005 | c0008 | t0001 | g0034 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03540 | hp2 | a0003 | c0003 | t0004 | g0086 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0220 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0257 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04204 | hp1 | a0006 | c0009 | t0001 | g0240 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04228 | hp1 | a0006 | c0009 | t0001 | g0219 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19043 | hp2 | a0003 | c0003 | t0003 | g0207 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19067 | hp1 | a0007 | c0011 | t0001 | g0268 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19240 | hp1 | a0001 | c0010 | t0001 | g0203 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20129 | hp2 | a0003 | c0003 | t0003 | g0210 | AFR | ASW | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20752 | hp2 | a0004 | c0005 | t0001 | g0026 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20905 | hp2 | a0002 | c0004 | t0001 | g0242 | SAS | GIH | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0237 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02109 | hp1 | a0003 | c0003 | t0004 | g0087 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02486 | hp1 | a0001 | c0006 | t0001 | g0204 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG03471 | hp2 | a0003 | c0003 | t0003 | g0209 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA21309 | hp1 | a0003 | c0003 | t0004 | g0037 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0206 | REF | REF | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0216 | REF | REF | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140389235
|
G | A | 1 | a0006 | 2 | HG04204.hp1 HG04228.hp1 |
stop_gained | HIGH | c.1822C>T | p.Arg608* | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 1943/2725 | 1822/1833 | 608/610 | chr4 | 140389235 | ||
chr4:140393998
|
T | G | 1 | a0005 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1193A>C | p.Glu398Ala | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/15 | 1314/2725 | 1193/1833 | 398/610 | chr4 | 140393998 | ||
chr4:140395914
|
G | A | 3 | a0002a0006a0007 | 60 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
missense_variant | MODERATE | c.1054C>T | p.Arg352Trp | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/15 | 1175/2725 | 1054/1833 | 352/610 | chr4 | 140395914 | ||
chr4:140398867
|
C | T | 1 | a0003 | 14 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.868G>A | p.Val290Ile | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 989/2725 | 868/1833 | 290/610 | chr4 | 140398867 | ||
chr4:140398927
|
G | A | 1 | a0004 | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
missense_variant | MODERATE | c.808C>T | p.Pro270Ser | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 929/2725 | 808/1833 | 270/610 | chr4 | 140398927 | ||
chr4:140402008
|
C | A | 1 | a0003 | 14 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.478G>T | p.Ala160Ser | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/15 | 599/2725 | 478/1833 | 160/610 | chr4 | 140402008 | ||
chr4:140405970
|
T | C | 1 | a0007 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.391A>G | p.Ile131Val | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/15 | 512/2725 | 391/1833 | 131/610 | chr4 | 140405970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140392346
|
G | A | 1 | a0001c0007 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.1524C>T | p.Thr508Thr | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/15 | 1645/2725 | 1524/1833 | 508/610 | chr4 | 140392346 | ||
chr4:140394000
|
G | A | 1 | a0001c0010 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1191C>T | p.Phe397Phe | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/15 | 1312/2725 | 1191/1833 | 397/610 | chr4 | 140394000 | ||
chr4:140398976
|
G | A | 1 | a0002c0004 | 5 | HG00642.hp2 HG01070.hp1 HG03490.hp1 others(2): Show |
synonymous_variant | LOW | c.759C>T | p.Leu253Leu | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 880/2725 | 759/1833 | 253/610 | chr4 | 140398976 | ||
chr4:140400496
|
A | G | 1 | a0001c0006 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.555T>C | p.Cys185Cys | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/15 | 676/2725 | 555/1833 | 185/610 | chr4 | 140400496 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140388548
|
A | G | 1 | a0003c0003t0003 | 9 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*676T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 676 | chr4 | 140388548 | |||||
chr4:140388603
|
C | T | 1 | a0001c0001t0005 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*621G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 621 | chr4 | 140388603 | |||||
chr4:140388946
|
A | G | 1 | a0001c0001t0008 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 278 | chr4 | 140388946 | |||||
chr4:140389072
|
T | G | 4 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(1): Show | 71 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*152A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 152 | chr4 | 140389072 | |||||
chr4:140427594
|
G | T | 2 | a0001c0001t0002a0001c0001t0008 | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14516 | chr4 | 140427594 | |||||
chr4:140427632
|
G | C | 1 | a0001c0001t0006 | 2 | HG02074.hp1 NA18965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-105C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14554 | chr4 | 140427632 | |||||
chr4:140427633
|
C | T | 1 | a0001c0001t0007 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14555 | chr4 | 140427633 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140389353
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-49T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389353 | ||||||
chr4:140389424
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1753-120T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389424 | ||||||
chr4:140389500
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1753-196A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389500 | ||||||
chr4:140389505
|
A | T | 1 | a0001c0006t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1753-201T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389505 | ||||||
chr4:140389515
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1753-211C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389515 | ||||||
chr4:140389547
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1753-243G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389547 | ||||||
chr4:140389694
|
C | T | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1753-390G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389694 | ||||||
chr4:140389702
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1753-398T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389702 | ||||||
chr4:140389739
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1753-435T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389739 | ||||||
chr4:140389869
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1753-565A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389869 | ||||||
chr4:140390008
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1752+620T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390008 | ||||||
chr4:140390048
|
T | C | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1752+580A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390048 | ||||||
chr4:140390074
|
T | A | 1 | a0002c0002t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1752+554A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390074 | ||||||
chr4:140390081
|
C | CA | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+546dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390081 | ||||||
chr4:140390115
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+513T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390115 | ||||||
chr4:140390132
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1752+496C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390132 | ||||||
chr4:140390384
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1752+244A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390384 | ||||||
chr4:140390553
|
T | C | 11 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(8): Show | 15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1752+75A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390553 | ||||||
chr4:140390596
|
C | T | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1752+32G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390596 | ||||||
chr4:140390806
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1652-78A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390806 | ||||||
chr4:140390809
|
G | A | 1 | a0002c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1652-81C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390809 | ||||||
chr4:140390966
|
G | A | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1652-238C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390966 | ||||||
chr4:140391096
|
A | G | 1 | a0002c0002t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1652-368T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391096 | ||||||
chr4:140391238
|
T | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1652-510A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391238 | ||||||
chr4:140391505
|
G | GTA | 12 | a0001c0001t0001g0239a0001c0001t0001g0253a0001c0001t0001g0262others(9): Show | 12 | HG00673.hp1 HG01123.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651+712_1651+713d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391505 | ||||||
chr4:140391722
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1651+497C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391722 | ||||||
chr4:140391891
|
C | T | 3 | a0002c0002t0001g0234a0002c0002t0001g0245a0002c0002t0001g0261 | 3 | HG01175.hp1 HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1651+328G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391891 | ||||||
chr4:140391936
|
A | C | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1651+283T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391936 | ||||||
chr4:140391961
|
C | T | 1 | a0002c0004t0001g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1651+258G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391961 | ||||||
chr4:140392427
|
T | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1492-49A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392427 | ||||||
chr4:140392429
|
A | G | 1 | a0003c0003t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1492-51T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392429 | ||||||
chr4:140392554
|
G | GA | 4 | a0001c0001t0002g0019a0001c0001t0002g0072a0001c0001t0002g0073others(1): Show | 5 | HG01433.hp1 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1491+31dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392554 | ||||||
chr4:140392719
|
C | T | 2 | a0003c0003t0001g0208a0003c0003t0003g0206 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
splice_region_variant&intron_variant | LOW | c.1366-8G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392719 | ||||||
chr4:140392876
|
A | G | 10 | a0003c0003t0001g0208a0003c0003t0003g0007a0003c0003t0003g0206others(7): Show | 14 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1366-165T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392876 | ||||||
chr4:140392902
|
G | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1366-191C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392902 | ||||||
chr4:140393040
|
A | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-329T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393040 | ||||||
chr4:140393147
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201 | 4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-436T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393147 | ||||||
chr4:140393178
|
T | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1366-467A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393178 | ||||||
chr4:140393216
|
C | T | 50 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1366-505G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393216 | ||||||
chr4:140393268
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0006g0279a0003c0003t0004g0037 | 4 | HG02074.hp1 HG02258.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-557C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393268 | ||||||
chr4:140393394
|
G | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1365+432C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393394 | ||||||
chr4:140393447
|
G | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0071 | 3 | NA18948.hp1 NA18983.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1365+379C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393447 | ||||||
chr4:140393568
|
A | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1365+258T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393568 | ||||||
chr4:140393609
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1365+217A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393609 | ||||||
chr4:140394102
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0184a0001c0001t0001g0185 | 4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-61T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394102 | ||||||
chr4:140394136
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1150-95G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394136 | ||||||
chr4:140394148
|
AAG | A | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1150-109_1150-108d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394148 | ||||||
chr4:140394227
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1150-186A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394227 | ||||||
chr4:140394233
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1150-192G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394233 | ||||||
chr4:140394234
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1150-193C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394234 | ||||||
chr4:140394364
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0232 | 2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1150-323T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394364 | ||||||
chr4:140394587
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1150-546A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394587 | ||||||
chr4:140394849
|
A | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1150-808T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394849 | ||||||
chr4:140394885
|
T | C | 7 | a0001c0001t0002g0005a0001c0001t0002g0016a0001c0001t0002g0046others(4): Show | 11 | HG01975.hp2 HG01978.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1150-844A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394885 | ||||||
chr4:140394914
|
G | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0184a0001c0001t0001g0185 | 4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-873C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394914 | ||||||
chr4:140394915
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0132a0001c0001t0001g0158others(1): Show | 5 | HG00140.hp1 HG01106.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150-874G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394915 | ||||||
chr4:140394928
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1150-887G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394928 | ||||||
chr4:140395006
|
G | A | 1 | a0001c0010t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1149+813C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395006 | ||||||
chr4:140395011
|
C | T | 7 | a0003c0003t0001g0208a0003c0003t0003g0007a0003c0003t0003g0206others(4): Show | 10 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+808G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395011 | ||||||
chr4:140395034
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1149+785C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395034 | ||||||
chr4:140395067
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1149+752G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395067 | ||||||
chr4:140395145
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1149+674A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395145 | ||||||
chr4:140395159
|
G | GT | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1149+659dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395159 | ||||||
chr4:140395167
|
G | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 342 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1149+652C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395167 | ||||||
chr4:140395292
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149+527C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395292 | ||||||
chr4:140395413
|
T | C | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1149+406A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395413 | ||||||
chr4:140395483
|
A | G | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1149+336T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395483 | ||||||
chr4:140395609
|
A | G | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1149+210T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395609 | ||||||
chr4:140395654
|
T | C | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1149+165A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395654 | ||||||
chr4:140395729
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1149+90G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395729 | ||||||
chr4:140396066
|
G | A | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.998+26C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 9/14 | chr4 | 140396066 | ||||||
chr4:140396510
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.885-305A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396510 | ||||||
chr4:140396646
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.885-441A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396646 | ||||||
chr4:140396750
|
G | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0174 | 2 | NA18998.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.885-545C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396750 | ||||||
chr4:140396862
|
C | CAT | 8 | a0001c0001t0001g0239a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 9 | HG01168.hp2 HG01256.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-659_885-658dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396862 | ||||||
chr4:140396862
|
CATATATA others(7): Show |
C | 6 | a0003c0003t0003g0007a0003c0003t0003g0209a0003c0003t0003g0210others(3): Show | 9 | HG01106.hp2 HG02109.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-671_885-658del others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396862 | ||||||
chr4:140396874
|
C | CAT | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.885-671_885-670dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | ||||||
chr4:140396874
|
C | CATAT | 5 | a0001c0001t0001g0031a0001c0001t0001g0129a0001c0001t0001g0153others(2): Show | 6 | HG00639.hp2 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.885-673_885-670dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | ||||||
chr4:140396874
|
C | T | 3 | a0001c0006t0001g0211a0003c0003t0001g0208a0003c0003t0003g0206 | 3 | HG00140.hp2 HG03139.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.885-669G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | ||||||
chr4:140396875
|
ATATATAT others(9): Show |
A | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.885-686_885-671del others(16): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396875 | ||||||
chr4:140396876
|
T | C | 3 | a0001c0006t0001g0211a0003c0003t0001g0208a0003c0003t0003g0206 | 3 | HG00140.hp2 HG03139.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.885-671A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396876 | ||||||
chr4:140396878
|
T | C | 1 | a0001c0006t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.885-673A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396878 | ||||||
chr4:140396884
|
T | C | 1 | a0001c0006t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.885-679A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396884 | ||||||
chr4:140396886
|
T | C | 1 | a0001c0006t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.885-681A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396886 | ||||||
chr4:140396889
|
A | ATATG | 9 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0098others(6): Show | 10 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885-685_885-684ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396889 | ||||||
chr4:140396889
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 7 | HG01243.hp2 HG01496.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.885-684T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396889 | ||||||
chr4:140396890
|
T | C | 6 | a0003c0003t0003g0007a0003c0003t0003g0209a0003c0003t0003g0210others(3): Show | 9 | HG01106.hp2 HG02109.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-685A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396890 | ||||||
chr4:140396890
|
T | TATAC | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.885-686_885-685ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396890 | ||||||
chr4:140396891
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0250others(16): Show | 27 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.885-686C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | ||||||
chr4:140396891
|
G | GTA | 53 | a0001c0001t0001g0014a0001c0001t0001g0101a0001c0001t0001g0217others(50): Show | 63 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.885-688_885-687dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | ||||||
chr4:140396891
|
G | GTATA | 8 | a0002c0002t0001g0015a0002c0002t0001g0041a0002c0002t0001g0233others(5): Show | 11 | HG00738.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.885-690_885-687dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | ||||||
chr4:140396891
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0232a0002c0002t0001g0236 | 2 | HG03209.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.885-687_885-686ins others(20): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | ||||||
chr4:140396893
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0104others(8): Show | 13 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.885-688T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396893 | ||||||
chr4:140396895
|
A | G | 1 | a0001c0010t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.885-690T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396895 | ||||||
chr4:140396897
|
A | G | 2 | a0001c0001t0001g0200a0001c0006t0001g0211 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.885-692T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396897 | ||||||
chr4:140396897
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201 | 4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-702_885-693del others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396897 | ||||||
chr4:140396898
|
T | C | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.885-693A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396898 | ||||||
chr4:140396899
|
A | G | 2 | a0001c0001t0001g0200a0001c0006t0001g0211 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.885-694T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396899 | ||||||
chr4:140396901
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-696T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396901 | ||||||
chr4:140396903
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-698T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396903 | ||||||
chr4:140396904
|
TATGTATA others(15): Show |
T | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.885-721_885-700del others(22): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396904 | ||||||
chr4:140396905
|
A | ATATG | 3 | a0001c0001t0001g0032a0001c0001t0001g0147a0002c0004t0001g0242 | 4 | HG01070.hp2 HG01071.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-701_885-700ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | ||||||
chr4:140396905
|
A | ATG | 4 | a0001c0001t0002g0005a0001c0001t0002g0056a0001c0001t0002g0058others(1): Show | 7 | HG01975.hp2 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-702_885-701dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | ||||||
chr4:140396905
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 13 | HG01891.hp1 HG02040.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.885-700T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | ||||||
chr4:140396907
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0032others(20): Show | 29 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.885-702C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | ||||||
chr4:140396907
|
G | GTA | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.885-704_885-703dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | ||||||
chr4:140396907
|
G | GTATA | 14 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0108others(11): Show | 17 | HG00438.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.885-706_885-703dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | ||||||
chr4:140396907
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0066a0001c0001t0002g0068 | 5 | NA18986.hp1 NA18999.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.885-703_885-702ins others(18): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | ||||||
chr4:140396922
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201 | 4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-717A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | ||||||
chr4:140396922
|
TAC | T | 3 | a0003c0003t0003g0007a0003c0003t0003g0210a0003c0003t0003g0247 | 6 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.885-719_885-718del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | ||||||
chr4:140396922
|
TACAC | T | 5 | a0003c0003t0001g0208a0003c0003t0003g0206a0003c0003t0003g0207others(2): Show | 5 | HG00140.hp2 HG02109.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.885-721_885-718del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | ||||||
chr4:140396924
|
C | T | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0003c0003t0003g0209 | 3 | HG02486.hp1 HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.885-719G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396924 | ||||||
chr4:140396926
|
C | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0258a0001c0006t0001g0204others(5): Show | 11 | HG01106.hp2 HG02300.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.885-721G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396926 | ||||||
chr4:140396943
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.885-738T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396943 | ||||||
chr4:140397068
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.885-863G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397068 | ||||||
chr4:140397114
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.885-909T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397114 | ||||||
chr4:140397128
|
T | A | 19 | a0002c0002t0001g0004a0002c0002t0001g0039a0002c0002t0001g0041others(16): Show | 27 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.885-923A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397128 | ||||||
chr4:140397454
|
G | C | 1 | a0001c0001t0002g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.885-1249C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397454 | ||||||
chr4:140397458
|
GT | G | 16 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0002g0061others(13): Show | 20 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.885-1254delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397458 | ||||||
chr4:140397632
|
G | A | 11 | a0001c0001t0001g0232a0003c0003t0001g0208a0003c0003t0003g0007others(8): Show | 15 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.884+1219C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397632 | ||||||
chr4:140397745
|
A | T | 1 | a0001c0001t0002g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.884+1106T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397745 | ||||||
chr4:140397779
|
C | G | 5 | a0003c0003t0003g0007a0003c0003t0003g0207a0003c0003t0003g0209others(2): Show | 8 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.884+1072G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397779 | ||||||
chr4:140397860
|
C | T | 2 | a0001c0001t0001g0187a0003c0003t0004g0037 | 3 | HG02258.hp1 NA18965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.884+991G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397860 | ||||||
chr4:140397861
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.884+990C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397861 | ||||||
chr4:140397890
|
C | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0054 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.884+961G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397890 | ||||||
chr4:140398229
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884+622A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398229 | ||||||
chr4:140398257
|
C | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0125 | 2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.884+594G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398257 | ||||||
chr4:140398263
|
C | CT | 67 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0023others(64): Show | 84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.884+587dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | ||||||
chr4:140398263
|
C | CTT | 15 | a0001c0001t0001g0112a0001c0001t0001g0173a0001c0001t0002g0016others(12): Show | 20 | HG01106.hp2 HG02109.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.884+586_884+587dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | ||||||
chr4:140398263
|
C | CTTT | 6 | a0001c0001t0002g0046a0001c0001t0002g0051a0001c0001t0002g0059others(3): Show | 6 | HG00558.hp2 HG02717.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.884+585_884+587dup others(3): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | ||||||
chr4:140398263
|
CT | C | 31 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0101others(28): Show | 36 | HG00280.hp2 HG00639.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.884+587delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | ||||||
chr4:140398308
|
C | T | 10 | a0003c0003t0001g0208a0003c0003t0003g0007a0003c0003t0003g0206others(7): Show | 14 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.884+543G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398308 | ||||||
chr4:140398343
|
C | T | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.884+508G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398343 | ||||||
chr4:140398418
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.884+433G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398418 | ||||||
chr4:140398431
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0184a0001c0001t0001g0185 | 4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+420C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398431 | ||||||
chr4:140398639
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.884+212T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398639 | ||||||
chr4:140398667
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.884+184T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398667 | ||||||
chr4:140398744
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884+107A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398744 | ||||||
chr4:140398782
|
C | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.884+69G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398782 | ||||||
chr4:140399210
|
A | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-170T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399210 | ||||||
chr4:140399311
|
C | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-271G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399311 | ||||||
chr4:140399314
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201 | 4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-274T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399314 | ||||||
chr4:140399319
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695-279C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399319 | ||||||
chr4:140399530
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.695-490T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399530 | ||||||
chr4:140399546
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-506C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399546 | ||||||
chr4:140399553
|
G | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.695-513C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399553 | ||||||
chr4:140399586
|
C | T | 2 | a0006c0009t0001g0219a0006c0009t0001g0240 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.695-546G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399586 | ||||||
chr4:140399587
|
C | A | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-547G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399587 | ||||||
chr4:140399620
|
T | G | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-580A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399620 | ||||||
chr4:140399679
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0174 | 2 | NA18998.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.695-639A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399679 | ||||||
chr4:140399975
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0112others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+382C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399975 | ||||||
chr4:140399981
|
G | A | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.694+376C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399981 | ||||||
chr4:140400028
|
T | G | 3 | a0001c0001t0002g0044a0001c0001t0002g0050a0001c0001t0002g0062 | 3 | HG00323.hp1 HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.694+329A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400028 | ||||||
chr4:140400045
|
T | C | 1 | a0002c0002t0001g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.694+312A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400045 | ||||||
chr4:140400227
|
T | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0201 | 4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+130A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400227 | ||||||
chr4:140400246
|
T | C | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.694+111A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400246 | ||||||
chr4:140400271
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.694+86T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400271 | ||||||
chr4:140400308
|
A | T | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694+49T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400308 | ||||||
chr4:140400578
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.502-29C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400578 | ||||||
chr4:140400652
|
G | C | 1 | a0002c0002t0001g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.502-103C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400652 | ||||||
chr4:140400663
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.502-114T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400663 | ||||||
chr4:140400730
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.502-181A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400730 | ||||||
chr4:140400860
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.502-311C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400860 | ||||||
chr4:140400998
|
A | G | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.502-449T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400998 | ||||||
chr4:140401045
|
C | T | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.502-496G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401045 | ||||||
chr4:140401082
|
C | T | 64 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(61): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.502-533G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401082 | ||||||
chr4:140401225
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.502-676T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401225 | ||||||
chr4:140401265
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.502-716G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401265 | ||||||
chr4:140401382
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.501+603A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401382 | ||||||
chr4:140401534
|
A | G | 5 | a0002c0004t0001g0127a0002c0004t0001g0220a0002c0004t0001g0227others(2): Show | 5 | HG00642.hp2 HG01070.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+451T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401534 | ||||||
chr4:140401639
|
A | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.501+346T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401639 | ||||||
chr4:140401909
|
A | T | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.501+76T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401909 | ||||||
chr4:140402088
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.420-22G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402088 | ||||||
chr4:140402115
|
G | A | 13 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(10): Show | 17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420-49C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402115 | ||||||
chr4:140402153
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.420-87A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402153 | ||||||
chr4:140402511
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.420-445A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402511 | ||||||
chr4:140402686
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420-620A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402686 | ||||||
chr4:140402714
|
GT | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.420-649delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402714 | ||||||
chr4:140402781
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.420-715G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402781 | ||||||
chr4:140402832
|
G | A | 1 | a0001c0001t0001g0033 | 2 | NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.420-766C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402832 | ||||||
chr4:140402945
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.420-879T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402945 | ||||||
chr4:140403037
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-971C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403037 | ||||||
chr4:140403155
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0046a0001c0001t0002g0059 | 4 | NA19004.hp1 NA19058.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.420-1089C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403155 | ||||||
chr4:140403219
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.420-1153G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403219 | ||||||
chr4:140403266
|
A | C | 3 | a0002c0002t0001g0015a0002c0002t0001g0233a0002c0002t0001g0257 | 5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.420-1200T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403266 | ||||||
chr4:140403345
|
C | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1279G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403345 | ||||||
chr4:140403408
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1342C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403408 | ||||||
chr4:140403416
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.420-1350A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403416 | ||||||
chr4:140403534
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0010t0001g0203 | 3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1468G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403534 | ||||||
chr4:140403562
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.420-1496G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403562 | ||||||
chr4:140403687
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.420-1621T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403687 | ||||||
chr4:140403719
|
C | T | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.420-1653G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403719 | ||||||
chr4:140404057
|
A | G | 15 | a0001c0001t0005g0020a0001c0001t0005g0088a0001c0006t0001g0204others(12): Show | 20 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.419+1885T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404057 | ||||||
chr4:140404095
|
A | T | 3 | a0001c0001t0001g0252a0002c0002t0001g0233a0002c0002t0001g0257 | 3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.419+1847T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404095 | ||||||
chr4:140404099
|
T | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0005g0020others(1): Show | 5 | HG01071.hp2 HG03017.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.419+1843A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404099 | ||||||
chr4:140404163
|
G | A | 7 | a0003c0003t0001g0208a0003c0003t0003g0007a0003c0003t0003g0206others(4): Show | 10 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.419+1779C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404163 | ||||||
chr4:140404255
|
G | A | 12 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.419+1687C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404255 | ||||||
chr4:140404283
|
C | T | 50 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.419+1659G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404283 | ||||||
chr4:140404284
|
A | G | 50 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.419+1658T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404284 | ||||||
chr4:140404328
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0213 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419+1614G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404328 | ||||||
chr4:140404378
|
G | C | 18 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0005g0020others(15): Show | 23 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.419+1564C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404378 | ||||||
chr4:140404584
|
A | G | 75 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(72): Show | 93 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.419+1358T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404584 | ||||||
chr4:140404655
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.419+1287G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404655 | ||||||
chr4:140404663
|
C | CT | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.419+1278dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404663 | ||||||
chr4:140404693
|
C | T | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.419+1249G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404693 | ||||||
chr4:140404773
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0002g0063a0001c0001t0002g0083 | 3 | NA18975.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.419+1169C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404773 | ||||||
chr4:140404813
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02698.hp2 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+1129G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404813 | ||||||
chr4:140404911
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.419+1031G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404911 | ||||||
chr4:140404935
|
CAT | C | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.419+1005_419+1006d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404935 | ||||||
chr4:140405138
|
ATTGT | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0112others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+800_419+803del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405138 | ||||||
chr4:140405169
|
T | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.419+773A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405169 | ||||||
chr4:140405171
|
TTA | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.419+769_419+770del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405171 | ||||||
chr4:140405172
|
TA | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0032others(22): Show | 30 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.419+769delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405172 | ||||||
chr4:140405173
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.419+769T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405173 | ||||||
chr4:140405177
|
T | A | 1 | a0002c0004t0001g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.419+765A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405177 | ||||||
chr4:140405178
|
T | A | 1 | a0003c0003t0003g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.419+764A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405178 | ||||||
chr4:140405178
|
T | TTA | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.419+763_419+764ins others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405178 | ||||||
chr4:140405179
|
A | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(7): Show | 15 | HG00642.hp2 HG02572.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.419+763T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405179 | ||||||
chr4:140405183
|
T | TA | 15 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(12): Show | 19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419+758_419+759ins others(1): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405183 | ||||||
chr4:140405184
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.419+758A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405184 | ||||||
chr4:140405185
|
T | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0256 | 4 | HG02280.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+757A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405185 | ||||||
chr4:140405190
|
T | A | 64 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(61): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.419+752A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405190 | ||||||
chr4:140405191
|
A | AT | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.419+750dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405191 | ||||||
chr4:140405191
|
A | T | 3 | a0001c0001t0001g0223a0001c0001t0005g0020a0001c0001t0005g0088 | 4 | HG02615.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+751T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405191 | ||||||
chr4:140405197
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.419+745A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405197 | ||||||
chr4:140405329
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0149 | 3 | HG00438.hp2 HG02027.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.419+613G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405329 | ||||||
chr4:140405333
|
C | T | 15 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(12): Show | 19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419+609G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405333 | ||||||
chr4:140405345
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.419+597G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405345 | ||||||
chr4:140405426
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.419+516A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405426 | ||||||
chr4:140405430
|
C | T | 15 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(12): Show | 19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419+512G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405430 | ||||||
chr4:140405533
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.419+409T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405533 | ||||||
chr4:140405629
|
T | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.419+313A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405629 | ||||||
chr4:140406126
|
T | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.278-43A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406126 | ||||||
chr4:140406252
|
C | CT | 8 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(5): Show | 9 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-170dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406252 | ||||||
chr4:140406252
|
C | CTT | 7 | a0003c0003t0001g0208a0003c0003t0003g0007a0003c0003t0003g0206others(4): Show | 10 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.278-171_278-170dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406252 | ||||||
chr4:140406441
|
C | T | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-358G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406441 | ||||||
chr4:140406612
|
T | C | 1 | a0003c0003t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.278-529A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406612 | ||||||
chr4:140406623
|
G | A | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.278-540C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406623 | ||||||
chr4:140406742
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.278-659A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406742 | ||||||
chr4:140406925
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-842G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406925 | ||||||
chr4:140406953
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278-870A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406953 | ||||||
chr4:140407047
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.278-964T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407047 | ||||||
chr4:140407058
|
T | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-975A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407058 | ||||||
chr4:140407209
|
G | A | 3 | a0002c0002t0001g0015a0002c0002t0001g0233a0002c0002t0001g0257 | 5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-1126C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407209 | ||||||
chr4:140407227
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.278-1144A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407227 | ||||||
chr4:140407328
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.278-1245G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407328 | ||||||
chr4:140407374
|
G | A | 25 | a0002c0002t0001g0015a0002c0002t0001g0040a0002c0002t0001g0221others(22): Show | 28 | HG00642.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-1291C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407374 | ||||||
chr4:140407494
|
A | C | 2 | a0001c0001t0001g0213a0001c0010t0001g0203 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.278-1411T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407494 | ||||||
chr4:140407497
|
C | T | 62 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.278-1414G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407497 | ||||||
chr4:140407586
|
C | CA | 30 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0149others(27): Show | 35 | HG00639.hp1 HG00673.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.278-1504dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | ||||||
chr4:140407586
|
C | CAAA | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-1506_278-1504d others(5): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | ||||||
chr4:140407586
|
CA | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 154 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.278-1504delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | ||||||
chr4:140407757
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.278-1674C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407757 | ||||||
chr4:140407789
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.278-1706A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407789 | ||||||
chr4:140407935
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-1852A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407935 | ||||||
chr4:140407950
|
T | A | 3 | a0002c0002t0001g0042a0002c0002t0001g0265a0002c0002t0001g0273 | 4 | NA18971.hp2 NA18997.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-1867A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407950 | ||||||
chr4:140407960
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.277+1877T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407960 | ||||||
chr4:140407997
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0226 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.277+1840T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407997 | ||||||
chr4:140408363
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.277+1474C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408363 | ||||||
chr4:140408458
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.277+1379A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408458 | ||||||
chr4:140408631
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.277+1206G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408631 | ||||||
chr4:140408668
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+1169T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408668 | ||||||
chr4:140408757
|
T | A | 62 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.277+1080A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408757 | ||||||
chr4:140408827
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+1010C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408827 | ||||||
chr4:140408860
|
C | CAT | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 173 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.277+975_277+976dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408860
|
C | CATAT | 18 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0093others(15): Show | 21 | HG00280.hp2 HG00558.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.277+973_277+976dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408860
|
C | CATATAT | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG02132.hp1 HG02630.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+971_277+976dup others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408860
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.277+967_277+976dup others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408860
|
CATAT | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.277+973_277+976del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408860
|
CATATATA others(1): Show |
C | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.277+969_277+976del others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | ||||||
chr4:140408882
|
T | TAC | 3 | a0001c0001t0002g0048a0001c0001t0002g0052a0001c0001t0002g0054 | 3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.277+954_277+955ins others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408882 | ||||||
chr4:140408884
|
T | C | 5 | a0001c0001t0002g0048a0001c0001t0002g0052a0001c0001t0002g0054others(2): Show | 5 | HG00438.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+953A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | ||||||
chr4:140408884
|
T | TAC | 4 | a0001c0001t0001g0178a0001c0001t0001g0217a0001c0001t0002g0056others(1): Show | 4 | HG01975.hp1 HG01975.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+951_277+952dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | ||||||
chr4:140408884
|
T | TACAC | 43 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(40): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.277+949_277+952dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | ||||||
chr4:140409036
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.277+801T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409036 | ||||||
chr4:140409225
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.277+612A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409225 | ||||||
chr4:140409372
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0144a0001c0001t0001g0145 | 4 | NA18966.hp2 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+465G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409372 | ||||||
chr4:140409417
|
G | A | 64 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(61): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.277+420C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409417 | ||||||
chr4:140409498
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.277+339T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409498 | ||||||
chr4:140409519
|
C | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+318G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409519 | ||||||
chr4:140409556
|
TG | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0225a0001c0001t0001g0228others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+280delC | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409556 | ||||||
chr4:140409557
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+280C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409557 | ||||||
chr4:140409809
|
A | G | 6 | a0001c0001t0001g0239a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 6 | HG01168.hp2 HG01256.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+28T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409809 | ||||||
chr4:140409984
|
T | A | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-89A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140409984 | ||||||
chr4:140410172
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-277C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140410172 | ||||||
chr4:140410341
|
C | T | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+212G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140410341 | ||||||
chr4:140410843
|
CAG | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0095a0001c0001t0001g0169others(2): Show | 6 | HG02155.hp2 NA18991.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-219_145-218del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140410843 | ||||||
chr4:140411196
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0172 | 2 | NA18992.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.145-570T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411196 | ||||||
chr4:140411245
|
T | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0047 | 4 | HG02523.hp1 NA18961.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-619A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411245 | ||||||
chr4:140411303
|
A | G | 1 | a0003c0003t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.145-677T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411303 | ||||||
chr4:140411408
|
G | C | 5 | a0002c0002t0001g0218a0002c0002t0001g0248a0002c0002t0001g0249others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-782C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411408 | ||||||
chr4:140411484
|
T | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-858A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411484 | ||||||
chr4:140411889
|
C | T | 2 | a0002c0002t0001g0235a0002c0002t0001g0236 | 2 | NA18986.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.144+1046G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411889 | ||||||
chr4:140412125
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.144+810C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412125 | ||||||
chr4:140412150
|
G | C | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.144+785C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412150 | ||||||
chr4:140412262
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.144+673G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412262 | ||||||
chr4:140412321
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.144+614G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412321 | ||||||
chr4:140412649
|
A | T | 3 | a0001c0006t0001g0204a0001c0006t0001g0205a0001c0006t0001g0211 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.144+286T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412649 | ||||||
chr4:140412873
|
G | A | 1 | a0001c0006t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.144+62C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412873 | ||||||
chr4:140413348
|
A | C | 1 | a0002c0002t0001g0270 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-9-261T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413348 | ||||||
chr4:140413363
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-9-276G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413363 | ||||||
chr4:140413497
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-410C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413497 | ||||||
chr4:140413498
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-411A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413498 | ||||||
chr4:140413574
|
C | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0225a0001c0001t0001g0228others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-487G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413574 | ||||||
chr4:140413588
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9-501C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413588 | ||||||
chr4:140413661
|
C | T | 50 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(47): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-9-574G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413661 | ||||||
chr4:140413664
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-577G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413664 | ||||||
chr4:140413694
|
T | A | 1 | a0001c0001t0002g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-9-607A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413694 | ||||||
chr4:140413707
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01358.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-9-620G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413707 | ||||||
chr4:140413708
|
G | A | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-621C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413708 | ||||||
chr4:140413794
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9-707A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413794 | ||||||
chr4:140413863
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9-776T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413863 | ||||||
chr4:140413949
|
A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-862T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413949 | ||||||
chr4:140413950
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-863G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413950 | ||||||
chr4:140413951
|
G | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-864C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413951 | ||||||
chr4:140413995
|
C | T | 1 | a0002c0004t0001g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-908G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413995 | ||||||
chr4:140414003
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-916C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414003 | ||||||
chr4:140414131
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-9-1044A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414131 | ||||||
chr4:140414142
|
G | A | 1 | a0001c0006t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-1055C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414142 | ||||||
chr4:140414166
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9-1079T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414166 | ||||||
chr4:140414275
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1188G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414275 | ||||||
chr4:140414290
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(4): Show | 11 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1203G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414290 | ||||||
chr4:140414387
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.-9-1300A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414387 | ||||||
chr4:140414388
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1301C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414388 | ||||||
chr4:140414413
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1326C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414413 | ||||||
chr4:140414459
|
T | A | 18 | a0001c0001t0001g0101a0001c0001t0001g0217a0001c0001t0001g0225others(15): Show | 18 | HG00639.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1372A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414459 | ||||||
chr4:140414510
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-9-1423G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414510 | ||||||
chr4:140414592
|
G | A | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1505C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414592 | ||||||
chr4:140414717
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-1630G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414717 | ||||||
chr4:140414735
|
A | G | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-1648T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414735 | ||||||
chr4:140414745
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-9-1658C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414745 | ||||||
chr4:140414787
|
C | T | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-1700G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414787 | ||||||
chr4:140414797
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1710G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414797 | ||||||
chr4:140414830
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-1743C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414830 | ||||||
chr4:140414895
|
T | C | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1808A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414895 | ||||||
chr4:140415129
|
C | A | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-2042G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415129 | ||||||
chr4:140415224
|
A | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0083 | 2 | NA18975.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-9-2137T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415224 | ||||||
chr4:140415236
|
C | G | 2 | a0006c0009t0001g0219a0006c0009t0001g0240 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-9-2149G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415236 | ||||||
chr4:140415262
|
A | G | 1 | a0003c0003t0003g0206 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9-2175T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415262 | ||||||
chr4:140415493
|
A | G | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-2406T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415493 | ||||||
chr4:140415588
|
T | A | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-9-2501A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415588 | ||||||
chr4:140415742
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9-2655T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415742 | ||||||
chr4:140415758
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9-2671A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415758 | ||||||
chr4:140415847
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9-2760C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415847 | ||||||
chr4:140415865
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-2778G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415865 | ||||||
chr4:140415892
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-9-2805T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415892 | ||||||
chr4:140415919
|
C | T | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-2832G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415919 | ||||||
chr4:140415921
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-9-2834G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415921 | ||||||
chr4:140415944
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-2857G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415944 | ||||||
chr4:140415954
|
A | G | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-2867T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415954 | ||||||
chr4:140415972
|
G | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-2885C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415972 | ||||||
chr4:140416059
|
G | A | 65 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(62): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2972C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416059 | ||||||
chr4:140416070
|
A | T | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-2983T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416070 | ||||||
chr4:140416136
|
A | G | 47 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(44): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9-3049T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416136 | ||||||
chr4:140416190
|
G | A | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-3103C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416190 | ||||||
chr4:140416210
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0054 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9-3123T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416210 | ||||||
chr4:140416332
|
G | A | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-3245C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416332 | ||||||
chr4:140416407
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-3320G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416407 | ||||||
chr4:140416409
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-3322T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416409 | ||||||
chr4:140416472
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-3385T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416472 | ||||||
chr4:140416479
|
A | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0092others(9): Show | 21 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-3392T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416479 | ||||||
chr4:140416496
|
G | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3409C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416496 | ||||||
chr4:140416528
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-9-3441A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416528 | ||||||
chr4:140416578
|
A | G | 15 | a0001c0001t0001g0099a0001c0001t0001g0213a0001c0006t0001g0204others(12): Show | 19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9-3491T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416578 | ||||||
chr4:140416612
|
C | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-9-3525G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416612 | ||||||
chr4:140416629
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3542T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416629 | ||||||
chr4:140416674
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3587C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416674 | ||||||
chr4:140416685
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3598T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416685 | ||||||
chr4:140416712
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3625G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416712 | ||||||
chr4:140416754
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3667A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416754 | ||||||
chr4:140416764
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3677C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416764 | ||||||
chr4:140416784
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3697C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416784 | ||||||
chr4:140416785
|
C | G | 3 | a0001c0001t0001g0099a0001c0001t0005g0020a0001c0001t0005g0088 | 4 | HG02818.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-3698G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416785 | ||||||
chr4:140416814
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3727T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416814 | ||||||
chr4:140416816
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-3729A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416816 | ||||||
chr4:140416880
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3793T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416880 | ||||||
chr4:140416895
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3808T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416895 | ||||||
chr4:140416921
|
C | T | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-3834G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416921 | ||||||
chr4:140416923
|
T | C | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3836A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416923 | ||||||
chr4:140416962
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3875G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416962 | ||||||
chr4:140416968
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3881A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416968 | ||||||
chr4:140416982
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9-3895G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416982 | ||||||
chr4:140417007
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3920C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417007 | ||||||
chr4:140417031
|
C | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(61): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-9-3944G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417031 | ||||||
chr4:140417116
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-9-4029A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417116 | ||||||
chr4:140417138
|
C | T | 1 | a0001c0006t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-4051G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417138 | ||||||
chr4:140417148
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-9-4061G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417148 | ||||||
chr4:140417150
|
A | G | 1 | a0002c0004t0001g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-4063T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417150 | ||||||
chr4:140417268
|
G | A | 62 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(59): Show | 78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9-4181C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417268 | ||||||
chr4:140417378
|
T | G | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-4291A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417378 | ||||||
chr4:140417410
|
T | A | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-4323A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417410 | ||||||
chr4:140417426
|
C | T | 1 | a0001c0006t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-4339G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417426 | ||||||
chr4:140417444
|
A | C | 1 | a0001c0001t0002g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-9-4357T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417444 | ||||||
chr4:140417456
|
T | C | 6 | a0001c0001t0002g0019a0001c0001t0002g0049a0001c0001t0002g0072others(3): Show | 8 | HG01346.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-4369A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417456 | ||||||
chr4:140417466
|
C | CA | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-4380dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417466 | ||||||
chr4:140417757
|
G | T | 12 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(9): Show | 16 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-4670C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417757 | ||||||
chr4:140417823
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9-4736G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417823 | ||||||
chr4:140417965
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9-4878G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417965 | ||||||
chr4:140418071
|
T | C | 2 | a0001c0001t0001g0213a0001c0010t0001g0203 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-4984A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418071 | ||||||
chr4:140418136
|
A | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5049T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418136 | ||||||
chr4:140418224
|
C | T | 1 | a0001c0006t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-5137G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418224 | ||||||
chr4:140418412
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-9-5325T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418412 | ||||||
chr4:140418539
|
G | A | 1 | a0003c0003t0004g0037 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-5452C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418539 | ||||||
chr4:140418572
|
T | C | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-5485A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418572 | ||||||
chr4:140418680
|
A | G | 1 | a0004c0005t0001g0025 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-9-5593T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418680 | ||||||
chr4:140418727
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-5640T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418727 | ||||||
chr4:140418741
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5654A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418741 | ||||||
chr4:140418745
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-9-5658T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418745 | ||||||
chr4:140418767
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5680T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418767 | ||||||
chr4:140418795
|
C | T | 2 | a0001c0001t0001g0225a0002c0002t0001g0269 | 2 | HG00639.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-9-5708G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418795 | ||||||
chr4:140418818
|
G | A | 1 | a0001c0010t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9-5731C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418818 | ||||||
chr4:140418868
|
A | T | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-5781T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418868 | ||||||
chr4:140418916
|
C | T | 1 | a0001c0001t0005g0020 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-5829G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418916 | ||||||
chr4:140418931
|
T | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-5844A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418931 | ||||||
chr4:140419181
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9-6094A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419181 | ||||||
chr4:140419197
|
C | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6110G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419197 | ||||||
chr4:140419213
|
G | GA | 11 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0172others(8): Show | 11 | HG01168.hp2 HG01175.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-6127dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419213 | ||||||
chr4:140419238
|
G | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-6151C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419238 | ||||||
chr4:140419239
|
T | A | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-6152A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419239 | ||||||
chr4:140419259
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-9-6172G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419259 | ||||||
chr4:140419423
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-6336C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419423 | ||||||
chr4:140419444
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9-6357G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419444 | ||||||
chr4:140419532
|
T | C | 1 | a0001c0006t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-6445A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419532 | ||||||
chr4:140419795
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212 | 7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-6708C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419795 | ||||||
chr4:140419858
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-9-6771G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419858 | ||||||
chr4:140419875
|
T | C | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-6788A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419875 | ||||||
chr4:140420096
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01192.hp2 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-7009A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420096 | ||||||
chr4:140420114
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-9-7027G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420114 | ||||||
chr4:140420158
|
A | G | 14 | a0001c0001t0001g0213a0001c0006t0001g0204a0001c0006t0001g0205others(11): Show | 18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-7071T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420158 | ||||||
chr4:140420343
|
T | A | 1 | a0003c0003t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+7194A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420343 | ||||||
chr4:140420363
|
T | C | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+7174A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420363 | ||||||
chr4:140420380
|
T | A | 12 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(9): Show | 17 | HG00408.hp2 HG02074.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+7157A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420380 | ||||||
chr4:140420553
|
T | TA | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-10+6983_-10+6984i others(3): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420553 | ||||||
chr4:140420554
|
T | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-10+6983A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420554 | ||||||
chr4:140420554
|
TA | T | 12 | a0001c0001t0001g0239a0001c0001t0001g0258a0001c0001t0002g0052others(9): Show | 13 | HG01123.hp1 HG01168.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10+6982delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420554 | ||||||
chr4:140420555
|
A | T | 10 | a0001c0001t0001g0213a0001c0001t0004g0193a0001c0001t0004g0194others(7): Show | 10 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+6982T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420555 | ||||||
chr4:140420556
|
A | T | 3 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0006t0001g0211 | 3 | HG02630.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6981T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420556 | ||||||
chr4:140420616
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-10+6921A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420616 | ||||||
chr4:140420742
|
C | T | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6795G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420742 | ||||||
chr4:140420768
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+6769C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420768 | ||||||
chr4:140420820
|
G | T | 2 | a0001c0001t0001g0091a0002c0004t0001g0127 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-10+6717C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420820 | ||||||
chr4:140421044
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+6493T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421044 | ||||||
chr4:140421279
|
T | G | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6258A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421279 | ||||||
chr4:140421283
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10+6254G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421283 | ||||||
chr4:140421316
|
C | A | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6221G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421316 | ||||||
chr4:140421361
|
T | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-10+6176A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421361 | ||||||
chr4:140421362
|
G | T | 1 | a0002c0002t0001g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-10+6175C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421362 | ||||||
chr4:140421379
|
T | G | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6158A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421379 | ||||||
chr4:140421413
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-10+6124T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421413 | ||||||
chr4:140421425
|
G | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-10+6112C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421425 | ||||||
chr4:140421469
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 9 | NA18939.hp1 NA18943.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+6068A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421469 | ||||||
chr4:140421598
|
A | AT | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10+5938dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421598 | ||||||
chr4:140421603
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-10+5934G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421603 | ||||||
chr4:140421697
|
C | T | 1 | a0002c0002t0001g0264 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10+5840G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421697 | ||||||
chr4:140421722
|
G | A | 3 | a0002c0002t0001g0015a0002c0002t0001g0233a0002c0002t0001g0257 | 5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5815C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421722 | ||||||
chr4:140421862
|
C | A | 1 | a0002c0002t0001g0274 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-10+5675G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421862 | ||||||
chr4:140421978
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-10+5559G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421978 | ||||||
chr4:140421979
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 147 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-10+5558T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421979 | ||||||
chr4:140422303
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-10+5234G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422303 | ||||||
chr4:140422772
|
T | C | 2 | a0001c0001t0001g0213a0001c0010t0001g0203 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10+4765A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422772 | ||||||
chr4:140422840
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+4697G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422840 | ||||||
chr4:140422928
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(12): Show | 23 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-10+4609A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422928 | ||||||
chr4:140422931
|
C | G | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+4606G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422931 | ||||||
chr4:140423043
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-10+4494A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423043 | ||||||
chr4:140423078
|
G | A | 63 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(60): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-10+4459C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423078 | ||||||
chr4:140423262
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10+4275T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423262 | ||||||
chr4:140423334
|
G | A | 3 | a0003c0003t0003g0007a0003c0003t0003g0209a0003c0003t0003g0210 | 6 | HG01106.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+4203C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423334 | ||||||
chr4:140423398
|
G | T | 2 | a0002c0002t0001g0267a0007c0011t0001g0268 | 2 | NA18963.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-10+4139C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423398 | ||||||
chr4:140423580
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+3957C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423580 | ||||||
chr4:140423888
|
A | T | 51 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(48): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10+3649T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423888 | ||||||
chr4:140423957
|
C | T | 1 | a0002c0002t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+3580G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423957 | ||||||
chr4:140424257
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+3280T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424257 | ||||||
chr4:140424300
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0117others(7): Show | 17 | HG00558.hp1 HG01358.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+3237G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424300 | ||||||
chr4:140424337
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0189 | 3 | HG02155.hp2 NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-10+3200C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424337 | ||||||
chr4:140424450
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-10+3087G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424450 | ||||||
chr4:140424454
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+3083C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424454 | ||||||
chr4:140424989
|
C | G | 1 | a0003c0003t0004g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+2548G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424989 | ||||||
chr4:140425114
|
T | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-10+2423A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425114 | ||||||
chr4:140425204
|
T | C | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+2333A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425204 | ||||||
chr4:140425348
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10+2189C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425348 | ||||||
chr4:140425427
|
A | AGGGTGTG others(1): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0044a0001c0001t0002g0075 | 5 | HG01192.hp1 NA18986.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2102_-10+2109d others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425427 | ||||||
chr4:140425429
|
G | GGT | 37 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0001g0103others(34): Show | 42 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+2106_-10+2107d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGT | 28 | a0001c0001t0001g0101a0001c0001t0001g0217a0001c0001t0001g0225others(25): Show | 38 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-10+2104_-10+2107d others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGTGT | 10 | a0001c0001t0001g0223a0001c0001t0004g0193a0002c0002t0001g0221others(7): Show | 10 | HG01952.hp1 HG02300.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+2102_-10+2107d others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGTGTG others(3): Show |
36 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(33): Show | 50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10+2107_-10+2108i others(12): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGTGTG others(5): Show |
4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG01346.hp2 HG02523.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2107_-10+2108i others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGTGTG others(4): Show |
1 | a0001c0001t0002g0045 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+2107_-10+2108i others(13): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-10+2098_-10+2107d others(12): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
GGT | G | 5 | a0001c0001t0001g0262a0001c0001t0005g0020a0001c0001t0005g0088others(2): Show | 6 | HG01070.hp1 HG01256.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2106_-10+2107d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
GGTGT | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(2): Show | 9 | HG02109.hp1 HG02572.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+2104_-10+2107d others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425429
|
GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-10+2096_-10+2107d others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | ||||||
chr4:140425431
|
T | TGTGTGG | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG00408.hp2 HG00558.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2105_-10+2106i others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425431 | ||||||
chr4:140425444
|
G | GTGTC | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0114others(3): Show | 6 | HG00323.hp2 HG01175.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2092_-10+2093i others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425444 | ||||||
chr4:140425446
|
G | GTC | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 154 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-10+2090_-10+2091i others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425446 | ||||||
chr4:140425448
|
G | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0005c0008t0001g0034 | 4 | HG01074.hp1 HG02559.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2089C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425448 | ||||||
chr4:140425622
|
C | CT | 22 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0036others(19): Show | 27 | HG00323.hp2 HG01175.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10+1914dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | ||||||
chr4:140425622
|
CT | C | 8 | a0001c0001t0001g0035a0001c0001t0002g0083a0001c0001t0002g0084others(5): Show | 9 | HG02109.hp1 HG02258.hp2 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+1914delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | ||||||
chr4:140425622
|
CTTT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(9): Show | 19 | HG00140.hp2 HG01106.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10+1912_-10+1914d others(5): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | ||||||
chr4:140425622
|
CTTTTTTT others(1): Show |
C | 16 | a0002c0002t0001g0004a0002c0002t0001g0041a0002c0002t0001g0042others(13): Show | 23 | HG00408.hp1 HG00597.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10+1907_-10+1914d others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | ||||||
chr4:140425645
|
T | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10+1892A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425645 | ||||||
chr4:140425694
|
T | A | 2 | a0001c0001t0001g0213a0001c0010t0001g0203 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10+1843A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425694 | ||||||
chr4:140425775
|
C | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(12): Show | 23 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-10+1762G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425775 | ||||||
chr4:140425876
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-10+1661C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425876 | ||||||
chr4:140426074
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0212others(14): Show | 25 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10+1463T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426074 | ||||||
chr4:140426115
|
G | A | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+1422C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426115 | ||||||
chr4:140426369
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 330 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-10+1168G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426369 | ||||||
chr4:140426867
|
T | A | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02698.hp2 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+670A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426867 | ||||||
chr4:140426894
|
G | T | 1 | a0001c0006t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-10+643C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426894 | ||||||
chr4:140426962
|
C | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0088 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-10+575G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426962 | ||||||
chr4:140427103
|
A | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 330 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-10+434T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427103 | ||||||
chr4:140427118
|
C | CG | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 324 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.-10+418dupC | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427118 | ||||||
chr4:140427122
|
C | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 6 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+415G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427122 | ||||||
chr4:140427123
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 6 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+414A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427123 | ||||||
chr4:140427177
|
C | T | 1 | a0001c0010t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+360G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427177 | ||||||
chr4:140427283
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 332 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.-10+254T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427283 | ||||||
chr4:140427351
|
G | T | 2 | a0003c0003t0004g0086a0003c0003t0004g0087 | 2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+186C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427351 | ||||||
chr4:140427408
|
G | A | 68 | a0001c0001t0001g0014a0001c0001t0001g0217a0001c0001t0001g0223others(65): Show | 81 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-10+129C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427408 | ||||||
chr4:140427448
|
GGGGGAAG others(4): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+78_-10+88delGC others(9): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427448 |