geneid | 56253 |
---|---|
ensemblid | ENSG00000109943.9 |
hgncid | 24313 |
symbol | CRTAM |
name | cytotoxic and regulatory T cell molecule |
refseq_nuc | NM_019604.4 |
refseq_prot | NP_062550.2 |
ensembl_nuc | ENST00000227348.9 |
ensembl_prot | ENSP00000227348.4 |
mane_status | MANE Select |
chr | chr11 |
start | 122838500 |
end | 122872643 |
strand | + |
ver | v1.2 |
region | chr11:122838500-122872643 |
region5000 | chr11:122833500-122877643 |
regionname0 | CRTAM_chr11_122838500_122872643 |
regionname5000 | CRTAM_chr11_122833500_122877643 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 393 | 199 | 25 | 49 | 85 | 11 | 28 | 70 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002 | 1/0 | 393 | 128 | 43 | 17 | 49 | 5 | 13 | 38 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003 | 0/0 | 393 | 64 | 0 | 4 | 54 | 0 | 6 | 39 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004 | 0/0 | 393 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005 | 0/0 | 393 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0006 | 0/0 | 393 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0007 | 0/0 | 393 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0008 | 0/0 | 393 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0009 | 0/0 | 393 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0010 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0011 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1182 | 192 | 19 | 48 | 85 | 11 | 28 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0002 | 1/0 | 1182 | 72 | 36 | 11 | 17 | 2 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0003 | 0/0 | 1182 | 63 | 0 | 3 | 54 | 0 | 6 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0004 | 0/0 | 1182 | 54 | 6 | 6 | 31 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0005 | 0/0 | 1182 | 6 | 5 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0006 | 0/0 | 1182 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0007 | 0/0 | 1182 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0008 | 0/0 | 1182 | 5 | 4 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0009 | 0/0 | 1182 | 5 | 0 | 0 | 4 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0010 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0011 | 0/0 | 1182 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0012 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0013 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0014 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0015 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0016 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0017 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0018 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0019 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
c0020 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1292 | 116 | 35 | 16 | 56 | 1 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0002 | 0/1 | 1292 | 87 | 8 | 25 | 26 | 9 | 18 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0003 | 0/0 | 1292 | 69 | 1 | 4 | 59 | 0 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0004 | 0/0 | 1292 | 59 | 10 | 6 | 32 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0005 | 1/0 | 1292 | 26 | 7 | 2 | 13 | 2 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0006 | 0/0 | 1292 | 22 | 6 | 8 | 4 | 0 | 4 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0007 | 0/0 | 1292 | 10 | 10 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0008 | 0/0 | 1292 | 9 | 0 | 8 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0009 | 0/0 | 1292 | 9 | 8 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0010 | 0/0 | 1292 | 7 | 7 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0011 | 0/0 | 1292 | 4 | 4 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0012 | 0/0 | 1292 | 3 | 0 | 2 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0013 | 0/0 | 1292 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0014 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0015 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0016 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0017 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
t0018 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1182 | 192 | 19 | 48 | 85 | 11 | 28 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0005 | 0/0 | 1182 | 6 | 5 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0018 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002 | 1/0 | 1182 | 72 | 36 | 11 | 17 | 2 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0004 | 0/0 | 1182 | 54 | 6 | 6 | 31 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0016 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0017 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003c0003 | 0/0 | 1182 | 63 | 0 | 3 | 54 | 0 | 6 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003c0014 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004c0006 | 0/0 | 1182 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004c0012 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0008 | 0/0 | 1182 | 5 | 4 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0010 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0015 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0006c0007 | 0/0 | 1182 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0007c0009 | 0/0 | 1182 | 5 | 0 | 0 | 4 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0008c0013 | 0/0 | 1182 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0009c0011 | 0/0 | 1182 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0010c0020 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0011c0019 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2473 | 88 | 10 | 13 | 56 | 1 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0002 | 0/1 | 2473 | 87 | 8 | 25 | 26 | 9 | 18 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0004 | 0/0 | 2473 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0007 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0008 | 0/0 | 2473 | 9 | 0 | 8 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0012 | 0/0 | 2473 | 3 | 0 | 2 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0016 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0001t0018 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0005t0001 | 0/0 | 2473 | 6 | 5 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0001c0018t0011 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0001 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0005 | 1/0 | 2473 | 25 | 6 | 2 | 13 | 2 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0006 | 0/0 | 2473 | 22 | 6 | 8 | 4 | 0 | 4 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0007 | 0/0 | 2473 | 7 | 7 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0009 | 0/0 | 2473 | 7 | 6 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0002t0010 | 0/0 | 2473 | 5 | 5 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0004t0001 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0004t0003 | 0/0 | 2473 | 3 | 1 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0004t0004 | 0/0 | 2473 | 49 | 3 | 6 | 29 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0016t0001 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0002c0017t0004 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003c0003t0003 | 0/0 | 2473 | 62 | 0 | 3 | 54 | 0 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003c0003t0017 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0003c0014t0003 | 0/0 | 2473 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004c0006t0004 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004c0012t0009 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0004c0012t0010 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0008t0001 | 0/0 | 2473 | 4 | 3 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0008t0014 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0010t0007 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0010t0015 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0005c0015t0004 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0006c0007t0001 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0007c0009t0003 | 0/0 | 2473 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0007c0009t0013 | 0/0 | 2473 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0008c0013t0011 | 0/0 | 2473 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0009c0011t0001 | 0/0 | 2473 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0010c0020t0005 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
a0011c0019t0009 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | copy fasta | chr11 | 122833500 | 122877643 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0001t0018g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0005t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0005t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0001c0018t0011g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0005g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0006g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0007g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0009g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0010g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0010g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0002t0010g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0004t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0016t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0002c0017t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0003t0017g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0003c0014t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0006t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0006t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0006t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0006t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0006t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0012t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0012t0010g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0004c0012t0010g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0008t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0008t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0008t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0008t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0010t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0010t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0010t0015g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0005c0015t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0006c0007t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0006c0007t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0006c0007t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0006c0007t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0006c0007t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0007c0009t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0007c0009t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0007c0009t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0007c0009t0013g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0007c0009t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0008c0013t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0008c0013t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0008c0013t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0009c0011t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0009c0011t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0009c0011t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0010c0020t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
a0011c0019t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0004 | t0004 | g0018 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00099 | hp2 | a0002 | c0004 | t0004 | g0292 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00140 | hp2 | a0002 | c0004 | t0004 | g0018 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | FIN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | FIN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00408 | hp2 | a0007 | c0009 | t0003 | g0019 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00423 | hp1 | a0003 | c0003 | t0003 | g0100 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00438 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00544 | hp1 | a0003 | c0003 | t0003 | g0298 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00544 | hp2 | a0002 | c0002 | t0005 | g0201 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00558 | hp1 | a0003 | c0003 | t0003 | g0318 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00597 | hp2 | a0002 | c0004 | t0004 | g0035 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00609 | hp1 | a0002 | c0002 | t0005 | g0031 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00621 | hp2 | a0002 | c0002 | t0006 | g0191 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0187 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00642 | hp2 | a0005 | c0008 | t0001 | g0363 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00673 | hp1 | a0003 | c0003 | t0003 | g0148 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00735 | hp2 | a0001 | c0001 | t0012 | g0212 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00738 | hp2 | a0002 | c0002 | t0006 | g0189 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00741 | hp1 | a0002 | c0004 | t0004 | g0046 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01070 | hp1 | a0002 | c0004 | t0004 | g0003 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01071 | hp1 | a0002 | c0004 | t0004 | g0003 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0092 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01081 | hp2 | a0002 | c0002 | t0006 | g0366 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01099 | hp1 | a0002 | c0002 | t0005 | g0246 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01099 | hp2 | a0002 | c0002 | t0006 | g0010 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01109 | hp1 | a0009 | c0011 | t0001 | g0229 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01167 | hp1 | a0002 | c0002 | t0009 | g0150 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01167 | hp2 | a0002 | c0004 | t0004 | g0011 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01243 | hp1 | a0002 | c0002 | t0006 | g0195 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0084 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01257 | hp2 | a0002 | c0002 | t0006 | g0010 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01258 | hp1 | a0002 | c0002 | t0006 | g0010 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0295 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01361 | hp2 | a0002 | c0002 | t0006 | g0192 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0072 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01496 | hp2 | a0001 | c0005 | t0001 | g0015 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0265 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01515 | hp2 | a0002 | c0002 | t0005 | g0365 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01517 | hp2 | a0002 | c0002 | t0005 | g0364 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01884 | hp2 | a0002 | c0002 | t0009 | g0068 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01891 | hp1 | a0004 | c0006 | t0004 | g0032 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0096 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01952 | hp2 | a0002 | c0002 | t0005 | g0214 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01981 | hp1 | a0003 | c0003 | t0003 | g0207 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01993 | hp1 | a0002 | c0004 | t0004 | g0274 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01993 | hp2 | a0002 | c0004 | t0004 | g0003 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02015 | hp1 | a0003 | c0003 | t0003 | g0141 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02015 | hp2 | a0002 | c0004 | t0004 | g0278 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0325 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02027 | hp2 | a0002 | c0004 | t0004 | g0356 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02040 | hp1 | a0003 | c0003 | t0003 | g0323 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0073 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02055 | hp1 | a0002 | c0002 | t0006 | g0329 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02055 | hp2 | a0002 | c0002 | t0010 | g0342 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02056 | hp1 | a0002 | c0002 | t0005 | g0203 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02074 | hp1 | a0002 | c0004 | t0004 | g0261 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02074 | hp2 | a0002 | c0004 | t0004 | g0316 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02080 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02080 | hp2 | a0002 | c0004 | t0004 | g0324 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02083 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02129 | hp1 | a0003 | c0003 | t0003 | g0307 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02135 | hp2 | a0003 | c0003 | t0003 | g0289 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02145 | hp1 | a0006 | c0007 | t0001 | g0355 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02145 | hp2 | a0004 | c0012 | t0010 | g0216 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0086 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CDX | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02165 | hp2 | a0002 | c0002 | t0006 | g0299 | EAS | CDX | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02257 | hp1 | a0002 | c0002 | t0009 | g0361 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02257 | hp2 | a0002 | c0004 | t0004 | g0276 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02258 | hp1 | a0004 | c0012 | t0010 | g0348 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02258 | hp2 | a0002 | c0002 | t0010 | g0343 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02273 | hp2 | a0003 | c0014 | t0003 | g0039 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02280 | hp1 | a0004 | c0006 | t0004 | g0056 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02451 | hp1 | a0010 | c0020 | t0005 | g0233 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0286 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02602 | hp2 | a0002 | c0002 | t0006 | g0193 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02615 | hp1 | a0002 | c0002 | t0005 | g0213 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02615 | hp2 | a0002 | c0002 | t0005 | g0336 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02622 | hp1 | a0002 | c0002 | t0009 | g0152 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02622 | hp2 | a0006 | c0007 | t0001 | g0354 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02630 | hp1 | a0005 | c0010 | t0007 | g0237 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02647 | hp1 | a0002 | c0002 | t0007 | g0331 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02683 | hp1 | a0003 | c0003 | t0003 | g0305 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02683 | hp2 | a0002 | c0002 | t0006 | g0196 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02698 | hp1 | a0007 | c0009 | t0013 | g0009 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02717 | hp1 | a0002 | c0002 | t0009 | g0185 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02717 | hp2 | a0002 | c0002 | t0006 | g0328 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02723 | hp1 | a0002 | c0002 | t0005 | g0283 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02723 | hp2 | a0001 | c0005 | t0001 | g0015 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02809 | hp1 | a0004 | c0006 | t0004 | g0222 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02809 | hp2 | a0008 | c0013 | t0011 | g0232 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02818 | hp1 | a0006 | c0007 | t0001 | g0353 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0330 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02895 | hp1 | a0005 | c0015 | t0004 | g0045 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0015 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02896 | hp2 | a0002 | c0002 | t0010 | g0341 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0344 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02897 | hp2 | a0001 | c0005 | t0001 | g0347 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02922 | hp2 | a0002 | c0002 | t0007 | g0062 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02965 | hp1 | a0002 | c0002 | t0007 | g0360 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02970 | hp1 | a0002 | c0002 | t0007 | g0332 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02970 | hp2 | a0002 | c0016 | t0001 | g0057 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02976 | hp1 | a0008 | c0013 | t0011 | g0234 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02976 | hp2 | a0002 | c0002 | t0006 | g0220 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03041 | hp1 | a0002 | c0004 | t0001 | g0058 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03098 | hp1 | a0002 | c0004 | t0003 | g0284 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03098 | hp2 | a0002 | c0004 | t0001 | g0357 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03130 | hp2 | a0002 | c0002 | t0009 | g0338 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03139 | hp2 | a0002 | c0002 | t0006 | g0051 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03195 | hp2 | a0002 | c0002 | t0007 | g0227 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03209 | hp1 | a0002 | c0002 | t0007 | g0327 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03209 | hp2 | a0001 | c0018 | t0011 | g0349 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0339 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03486 | hp1 | a0008 | c0013 | t0011 | g0235 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0362 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03491 | hp1 | a0002 | c0004 | t0004 | g0011 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03491 | hp2 | a0002 | c0002 | t0006 | g0194 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03492 | hp2 | a0002 | c0004 | t0004 | g0011 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03516 | hp2 | a0002 | c0002 | t0009 | g0151 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03540 | hp2 | a0005 | c0008 | t0001 | g0236 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03579 | hp1 | a0005 | c0008 | t0001 | g0177 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03579 | hp2 | a0002 | c0002 | t0005 | g0153 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03654 | hp2 | a0003 | c0003 | t0003 | g0038 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0333 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03688 | hp2 | a0002 | c0004 | t0004 | g0041 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03704 | hp1 | a0003 | c0003 | t0003 | g0303 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03927 | hp1 | a0002 | c0004 | t0004 | g0041 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03927 | hp2 | a0002 | c0004 | t0004 | g0003 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04115 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04184 | hp1 | a0001 | c0001 | t0016 | g0169 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04184 | hp2 | a0003 | c0003 | t0017 | g0251 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04199 | hp1 | a0001 | c0001 | t0018 | g0182 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04199 | hp2 | a0002 | c0002 | t0006 | g0190 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04204 | hp1 | a0002 | c0004 | t0004 | g0223 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04204 | hp2 | a0002 | c0004 | t0004 | g0105 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG04228 | hp2 | a0002 | c0002 | t0005 | g0205 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18522 | hp1 | a0002 | c0002 | t0007 | g0359 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18522 | hp2 | a0004 | c0006 | t0004 | g0217 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18612 | hp1 | a0003 | c0003 | t0003 | g0297 | EAS | CHB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18906 | hp1 | a0005 | c0008 | t0014 | g0285 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18906 | hp2 | a0004 | c0012 | t0009 | g0239 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18942 | hp1 | a0003 | c0003 | t0003 | g0304 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18942 | hp2 | a0002 | c0004 | t0003 | g0034 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18946 | hp1 | a0003 | c0003 | t0003 | g0320 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18947 | hp1 | a0002 | c0004 | t0004 | g0264 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18947 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18948 | hp1 | a0002 | c0002 | t0005 | g0031 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18948 | hp2 | a0002 | c0004 | t0004 | g0256 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18949 | hp1 | a0002 | c0004 | t0004 | g0241 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18951 | hp2 | a0002 | c0002 | t0005 | g0186 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18952 | hp2 | a0002 | c0002 | t0005 | g0030 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18953 | hp1 | a0007 | c0009 | t0013 | g0158 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18956 | hp2 | a0003 | c0003 | t0003 | g0300 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18957 | hp1 | a0003 | c0003 | t0003 | g0312 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18957 | hp2 | a0002 | c0004 | t0004 | g0078 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18959 | hp1 | a0002 | c0002 | t0005 | g0202 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0294 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18961 | hp1 | a0003 | c0003 | t0003 | g0280 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18963 | hp1 | a0003 | c0003 | t0003 | g0326 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18966 | hp2 | a0002 | c0002 | t0005 | g0030 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18968 | hp2 | a0003 | c0003 | t0003 | g0315 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18969 | hp1 | a0003 | c0003 | t0003 | g0306 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18969 | hp2 | a0002 | c0002 | t0005 | g0066 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0023 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18972 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18973 | hp1 | a0003 | c0003 | t0003 | g0140 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18974 | hp1 | a0003 | c0003 | t0003 | g0302 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18977 | hp1 | a0002 | c0004 | t0004 | g0269 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0287 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18980 | hp2 | a0003 | c0003 | t0003 | g0147 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18981 | hp2 | a0002 | c0004 | t0004 | g0250 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18982 | hp1 | a0002 | c0004 | t0004 | g0037 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18982 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18984 | hp1 | a0002 | c0004 | t0004 | g0198 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18985 | hp1 | a0003 | c0003 | t0003 | g0319 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18985 | hp2 | a0002 | c0002 | t0005 | g0208 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18986 | hp1 | a0002 | c0002 | t0005 | g0127 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18987 | hp1 | a0002 | c0004 | t0004 | g0134 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18989 | hp1 | a0003 | c0003 | t0003 | g0296 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18989 | hp2 | a0002 | c0004 | t0004 | g0145 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18990 | hp1 | a0002 | c0004 | t0004 | g0273 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18992 | hp2 | a0003 | c0003 | t0003 | g0311 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18994 | hp2 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18998 | hp1 | a0002 | c0002 | t0006 | g0080 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18998 | hp2 | a0002 | c0004 | t0004 | g0197 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18999 | hp1 | a0002 | c0002 | t0005 | g0115 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA18999 | hp2 | a0003 | c0003 | t0003 | g0040 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19001 | hp1 | a0002 | c0004 | t0004 | g0076 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19001 | hp2 | a0002 | c0004 | t0004 | g0065 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19006 | hp1 | a0002 | c0004 | t0004 | g0255 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19010 | hp1 | a0002 | c0004 | t0004 | g0160 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19011 | hp1 | a0003 | c0003 | t0003 | g0308 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19012 | hp2 | a0002 | c0004 | t0003 | g0034 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19030 | hp2 | a0005 | c0010 | t0007 | g0228 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19043 | hp1 | a0002 | c0004 | t0004 | g0055 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19043 | hp2 | a0002 | c0002 | t0005 | g0206 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19054 | hp2 | a0003 | c0003 | t0003 | g0040 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19057 | hp1 | a0003 | c0003 | t0003 | g0290 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19057 | hp2 | a0002 | c0004 | t0004 | g0268 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19058 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19060 | hp2 | a0003 | c0003 | t0003 | g0039 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19062 | hp2 | a0003 | c0003 | t0003 | g0293 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19063 | hp1 | a0002 | c0002 | t0006 | g0322 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19063 | hp2 | a0002 | c0004 | t0004 | g0036 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19066 | hp1 | a0003 | c0003 | t0003 | g0121 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19068 | hp2 | a0002 | c0004 | t0004 | g0037 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19070 | hp2 | a0002 | c0017 | t0004 | g0036 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19072 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19074 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19076 | hp1 | a0003 | c0003 | t0003 | g0301 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19077 | hp1 | a0002 | c0004 | t0004 | g0270 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19078 | hp2 | a0003 | c0003 | t0003 | g0149 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19079 | hp2 | a0002 | c0004 | t0004 | g0267 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19081 | hp1 | a0002 | c0004 | t0004 | g0035 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19081 | hp2 | a0007 | c0009 | t0003 | g0061 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19084 | hp1 | a0003 | c0003 | t0003 | g0023 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19084 | hp2 | a0002 | c0004 | t0004 | g0272 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19086 | hp1 | a0002 | c0002 | t0005 | g0199 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19086 | hp2 | a0007 | c0009 | t0003 | g0262 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19091 | hp1 | a0003 | c0003 | t0003 | g0291 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19240 | hp1 | a0009 | c0011 | t0001 | g0238 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA19240 | hp2 | a0002 | c0002 | t0006 | g0052 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0048 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20905 | hp1 | a0002 | c0004 | t0004 | g0047 | SAS | GIH | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0350 | SAS | GIH | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG01123 | hp2 | a0002 | c0002 | t0006 | g0221 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02109 | hp1 | a0004 | c0006 | t0004 | g0218 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02109 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02486 | hp1 | a0002 | c0004 | t0004 | g0183 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02486 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0219 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG02559 | hp2 | a0002 | c0002 | t0006 | g0053 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03471 | hp1 | a0005 | c0008 | t0001 | g0043 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG03471 | hp2 | a0002 | c0002 | t0010 | g0184 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG06807 | hp1 | a0009 | c0011 | t0001 | g0231 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
HG06807 | hp2 | a0006 | c0007 | t0001 | g0358 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20300 | hp1 | a0011 | c0019 | t0009 | g0176 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA20300 | hp2 | a0004 | c0006 | t0004 | g0032 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA21309 | hp1 | a0005 | c0010 | t0015 | g0230 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
NA21309 | hp2 | a0002 | c0002 | t0005 | g0335 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0171 | REF | REF | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0005 | g0225 | REF | REF | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:122850068
|
A | C | 2 | a0008a0010 | 4 | HG02451.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.47A>C | p.Glu16Ala | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/10 | 94/2473 | 47/1182 | 16/393 | chr11 | 122850068 | ||
chr11:122851732
|
C | A | 4 | a0005a0008a0009others(1): Show | 16 | HG00642.hp2 HG01109.hp1 HG02451.hp1 others(13): Show |
missense_variant | MODERATE | c.233C>A | p.Ala78Asp | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/10 | 280/2473 | 233/1182 | 78/393 | chr11 | 122851732 | ||
chr11:122855722
|
A | G | 1 | a0006 | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.518A>G | p.Asp173Gly | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/10 | 565/2473 | 518/1182 | 173/393 | chr11 | 122855722 | ||
chr11:122862479
|
C | T | 1 | a0011 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.668C>T | p.Thr223Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/10 | 715/2473 | 668/1182 | 223/393 | chr11 | 122862479 | ||
chr11:122864660
|
C | T | 1 | a0004 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
missense_variant | MODERATE | c.758C>T | p.Thr253Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/10 | 805/2473 | 758/1182 | 253/393 | chr11 | 122864660 | ||
chr11:122867553
|
A | G | 5 | a0001a0006a0007others(2): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
missense_variant&splice_region_variant | MODERATE | c.962A>G | p.Lys321Arg | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/10 | 1009/2473 | 962/1182 | 321/393 | chr11 | 122867553 | ||
chr11:122871320
|
C | G | 2 | a0003a0007 | 69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
missense_variant | MODERATE | c.1103C>G | p.Ala368Gly | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1150/2473 | 1103/1182 | 368/393 | chr11 | 122871320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:122850099
|
C | A | 1 | a0003c0014 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.78C>A | p.Ile26Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/10 | 125/2473 | 78/1182 | 26/393 | chr11 | 122850099 | ||
chr11:122854037
|
G | A | 1 | a0001c0005 | 6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
synonymous_variant | LOW | c.441G>A | p.Lys147Lys | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/10 | 488/2473 | 441/1182 | 147/393 | chr11 | 122854037 | ||
chr11:122855783
|
G | A | 5 | a0002c0016a0005c0008a0005c0015others(2): Show | 11 | HG00642.hp2 HG02451.hp1 HG02809.hp2 others(8): Show |
synonymous_variant | LOW | c.579G>A | p.Thr193Thr | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/10 | 626/2473 | 579/1182 | 193/393 | chr11 | 122855783 | ||
chr11:122871276
|
C | T | 1 | a0002c0017 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.1059C>T | p.His353His | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1106/2473 | 1059/1182 | 353/393 | chr11 | 122871276 | ||
chr11:122871342
|
T | C | 6 | a0001c0018a0002c0004a0002c0017others(3): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
synonymous_variant | LOW | c.1125T>C | p.Asn375Asn | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1172/2473 | 1125/1182 | 375/393 | chr11 | 122871342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:122871446
|
C | A | 3 | a0002c0002t0006a0002c0002t0010a0004c0012t0010 | 29 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*47C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 47 | chr11 | 122871446 | |||||
chr11:122871616
|
A | C | 1 | a0001c0001t0018 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 217 | chr11 | 122871616 | |||||
chr11:122871720
|
T | G | 10 | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(7): Show | 126 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 321 | chr11 | 122871720 | |||||
chr11:122871752
|
A | T | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 353 | chr11 | 122871752 | |||||
chr11:122872035
|
T | A | 5 | a0001c0018t0011a0002c0002t0009a0004c0012t0009others(2): Show | 13 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*636T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 636 | chr11 | 122872035 | |||||
chr11:122872099
|
C | A | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0016others(1): Show | 92 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 700 | chr11 | 122872099 | |||||
chr11:122872113
|
C | T | 1 | a0001c0001t0016 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 714 | chr11 | 122872113 | |||||
chr11:122872114
|
A | G | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*715A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 715 | chr11 | 122872114 | |||||
chr11:122872171
|
G | C | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(6): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*772G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 772 | chr11 | 122872171 | |||||
chr11:122872208
|
T | C | 1 | a0005c0008t0014 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 809 | chr11 | 122872208 | |||||
chr11:122872242
|
G | A | 5 | a0001c0018t0011a0002c0002t0009a0004c0012t0009others(2): Show | 13 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*843G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 843 | chr11 | 122872242 | |||||
chr11:122872295
|
A | T | 2 | a0002c0002t0010a0004c0012t0010 | 7 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 896 | chr11 | 122872295 | |||||
chr11:122872335
|
T | C | 1 | a0005c0010t0015 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 936 | chr11 | 122872335 | |||||
chr11:122872345
|
A | G | 1 | a0001c0001t0008 | 9 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*946A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 946 | chr11 | 122872345 | |||||
chr11:122872446
|
T | C | 1 | a0007c0009t0013 | 2 | HG02698.hp1 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1047T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1047 | chr11 | 122872446 | |||||
chr11:122872496
|
T | C | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0016others(1): Show | 92 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1097T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1097 | chr11 | 122872496 | |||||
chr11:122872515
|
G | A | 1 | a0001c0001t0012 | 3 | HG00639.hp2 HG00735.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1116G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1116 | chr11 | 122872515 | |||||
chr11:122872632
|
C | T | 1 | a0003c0003t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1233 | chr11 | 122872632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:122838843
|
C | T | 3 | a0002c0002t0005g0364a0002c0002t0005g0365a0002c0002t0006g0366 | 3 | HG01081.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.46+251C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122838843 | ||||||
chr11:122838894
|
T | G | 5 | a0001c0001t0001g0044a0001c0005t0001g0042a0005c0008t0001g0043others(2): Show | 6 | HG02109.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+302T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122838894 | ||||||
chr11:122838925
|
T | TTTTA | 26 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0351others(23): Show | 31 | HG00642.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+351_46+354dupTT others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122838925 | |||||
chr11:122839029
|
C | T | 1 | a0005c0008t0001g0363 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.46+437C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839029 | ||||||
chr11:122839077
|
C | T | 1 | a0001c0001t0002g0340 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.46+485C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839077 | ||||||
chr11:122839093
|
G | C | 4 | a0001c0001t0012g0048a0002c0004t0004g0018a0002c0004t0004g0046others(1): Show | 5 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+501G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839093 | ||||||
chr11:122839154
|
A | G | 1 | a0002c0002t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+562A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839154 | ||||||
chr11:122839181
|
C | T | 1 | a0002c0002t0009g0338 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+589C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839181 | ||||||
chr11:122839187
|
C | A | 10 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+595C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839187 | ||||||
chr11:122839227
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.46+635C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839227 | ||||||
chr11:122839477
|
A | G | 2 | a0001c0001t0002g0337a0002c0002t0005g0336 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.46+885A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839477 | ||||||
chr11:122839548
|
A | G | 1 | a0002c0002t0005g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46+956A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839548 | ||||||
chr11:122839573
|
G | A | 3 | a0001c0001t0001g0019a0007c0009t0003g0019a0007c0009t0003g0061 | 3 | HG00408.hp2 NA18961.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.46+981G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839573 | ||||||
chr11:122839673
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.46+1081A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839673 | ||||||
chr11:122839804
|
C | A | 1 | a0002c0002t0007g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46+1212C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839804 | ||||||
chr11:122839853
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.46+1261T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839853 | ||||||
chr11:122839933
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.46+1341A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839933 | ||||||
chr11:122840024
|
C | T | 1 | a0003c0003t0003g0333 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.46+1432C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840024 | ||||||
chr11:122840159
|
A | G | 11 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+1567A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840159 | ||||||
chr11:122840263
|
T | C | 1 | a0002c0004t0004g0223 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46+1671T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840263 | ||||||
chr11:122840271
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.46+1679G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840271 | ||||||
chr11:122840307
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+1715T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840307 | ||||||
chr11:122840420
|
C | CGT | 14 | a0001c0001t0001g0063a0001c0001t0002g0215a0001c0005t0001g0219others(11): Show | 15 | HG01123.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.46+1847_46+1848dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122840420 | |||||
chr11:122840544
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.46+1952G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840544 | ||||||
chr11:122840582
|
A | T | 1 | a0002c0002t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+1990A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840582 | ||||||
chr11:122840655
|
C | T | 38 | a0001c0001t0001g0200a0001c0001t0001g0204a0001c0001t0001g0209others(35): Show | 42 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.46+2063C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840655 | ||||||
chr11:122841007
|
G | T | 47 | a0001c0001t0001g0154a0001c0001t0002g0009a0001c0001t0002g0025others(44): Show | 53 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+2415G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841007 | ||||||
chr11:122841111
|
T | C | 5 | a0001c0001t0001g0345a0002c0002t0010g0341a0002c0002t0010g0342others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2519T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841111 | ||||||
chr11:122841128
|
G | A | 3 | a0002c0002t0001g0330a0002c0002t0007g0331a0002c0002t0007g0332 | 3 | HG02647.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.46+2536G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841128 | ||||||
chr11:122841181
|
A | G | 1 | a0002c0002t0006g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.46+2589A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841181 | ||||||
chr11:122841247
|
C | T | 7 | a0001c0001t0001g0044a0001c0005t0001g0042a0002c0002t0006g0328others(4): Show | 8 | HG02109.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.46+2655C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841247 | ||||||
chr11:122841281
|
A | C | 53 | a0001c0001t0001g0288a0001c0001t0001g0314a0001c0001t0001g0317others(50): Show | 65 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.46+2689A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841281 | ||||||
chr11:122841404
|
A | AT | 84 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0154others(81): Show | 96 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.46+2826dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | |||||
chr11:122841404
|
A | ATT | 69 | a0001c0001t0001g0012a0001c0001t0001g0247a0001c0001t0001g0248others(66): Show | 79 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.46+2825_46+2826dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | |||||
chr11:122841404
|
ATT | A | 20 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0002g0050others(17): Show | 21 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.46+2825_46+2826del others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | |||||
chr11:122841436
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+2844C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841436 | ||||||
chr11:122841475
|
A | G | 1 | a0001c0001t0002g0340 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.46+2883A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841475 | ||||||
chr11:122841494
|
G | T | 5 | a0001c0001t0001g0345a0002c0002t0010g0341a0002c0002t0010g0342others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2902G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841494 | ||||||
chr11:122841642
|
C | T | 1 | a0001c0001t0018g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46+3050C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841642 | ||||||
chr11:122841695
|
C | T | 1 | a0002c0002t0005g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.46+3103C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841695 | ||||||
chr11:122841752
|
T | C | 1 | a0002c0004t0004g0241 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.46+3160T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841752 | ||||||
chr11:122841829
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+3237A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841829 | ||||||
chr11:122841878
|
A | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(306): Show | 358 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.46+3286A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841878 | ||||||
chr11:122841880
|
T | A | 1 | a0005c0008t0001g0363 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.46+3288T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841880 | ||||||
chr11:122841948
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46+3356A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841948 | ||||||
chr11:122842141
|
C | T | 2 | a0004c0012t0009g0239a0009c0011t0001g0238 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+3549C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842141 | ||||||
chr11:122842220
|
G | A | 2 | a0002c0002t0005g0283a0002c0004t0003g0284 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.46+3628G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842220 | ||||||
chr11:122842267
|
A | ATGTT | 10 | a0002c0002t0001g0330a0002c0002t0001g0339a0002c0002t0006g0322others(7): Show | 13 | HG02027.hp1 HG02040.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.46+3700_46+3703dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122842267 | |||||
chr11:122842267
|
ATGTT | A | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | NA18952.hp1 NA18974.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.46+3700_46+3703del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122842267 | |||||
chr11:122842294
|
T | C | 1 | a0002c0002t0007g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46+3702T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842294 | ||||||
chr11:122842483
|
C | T | 1 | a0001c0001t0001g0346 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.46+3891C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842483 | ||||||
chr11:122842517
|
G | C | 1 | a0002c0002t0006g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.46+3925G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842517 | ||||||
chr11:122842526
|
G | C | 2 | a0001c0018t0011g0349a0004c0012t0010g0348 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46+3934G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842526 | ||||||
chr11:122842588
|
A | G | 1 | a0001c0001t0002g0321 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.46+3996A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842588 | ||||||
chr11:122842627
|
T | A | 53 | a0001c0001t0001g0288a0001c0001t0001g0314a0001c0001t0001g0317others(50): Show | 65 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.46+4035T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842627 | ||||||
chr11:122842711
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46+4119A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842711 | ||||||
chr11:122842762
|
G | A | 1 | a0002c0002t0007g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46+4170G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842762 | ||||||
chr11:122842762
|
G | C | 1 | a0002c0004t0004g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.46+4170G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842762 | ||||||
chr11:122842794
|
C | T | 5 | a0002c0002t0001g0362a0002c0002t0007g0359a0002c0002t0007g0360others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+4202C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842794 | ||||||
chr11:122842850
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.46+4258C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842850 | ||||||
chr11:122842866
|
A | G | 2 | a0004c0012t0009g0239a0009c0011t0001g0238 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+4274A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842866 | ||||||
chr11:122842878
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.46+4286T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842878 | ||||||
chr11:122842896
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.46+4304C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842896 | ||||||
chr11:122842903
|
C | T | 2 | a0003c0003t0003g0319a0003c0003t0003g0320 | 2 | NA18946.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.46+4311C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842903 | ||||||
chr11:122842936
|
G | A | 1 | a0002c0002t0005g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.46+4344G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842936 | ||||||
chr11:122843102
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.46+4510A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843102 | ||||||
chr11:122843109
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.46+4517G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843109 | ||||||
chr11:122843424
|
G | A | 1 | a0002c0002t0005g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.46+4832G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843424 | ||||||
chr11:122843501
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0005t0001g0219others(4): Show | 9 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.46+4909C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843501 | ||||||
chr11:122843665
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46+5073C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843665 | ||||||
chr11:122843811
|
A | G | 1 | a0006c0007t0001g0358 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.46+5219A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843811 | ||||||
chr11:122843856
|
A | T | 1 | a0005c0010t0007g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.46+5264A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843856 | ||||||
chr11:122843888
|
G | A | 1 | a0002c0002t0001g0362 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46+5296G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843888 | ||||||
chr11:122844074
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.46+5482A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844074 | ||||||
chr11:122844117
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0069a0001c0001t0001g0070 | 6 | HG02056.hp2 HG02135.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+5525G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844117 | ||||||
chr11:122844760
|
A | T | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-5308A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844760 | ||||||
chr11:122844907
|
G | A | 11 | a0002c0002t0007g0227a0005c0008t0014g0285a0005c0010t0007g0228others(8): Show | 11 | HG01109.hp1 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.47-5161G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844907 | ||||||
chr11:122844938
|
A | G | 10 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.47-5130A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844938 | ||||||
chr11:122845018
|
G | A | 16 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5050G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845018 | ||||||
chr11:122845088
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.47-4980G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845088 | ||||||
chr11:122845155
|
G | A | 1 | a0002c0004t0004g0241 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.47-4913G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845155 | ||||||
chr11:122845195
|
C | T | 1 | a0005c0008t0001g0236 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47-4873C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845195 | ||||||
chr11:122845214
|
G | A | 1 | a0001c0001t0008g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.47-4854G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845214 | ||||||
chr11:122845235
|
G | C | 3 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0347 | 5 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-4833G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845235 | ||||||
chr11:122845288
|
A | G | 2 | a0001c0005t0001g0015a0001c0005t0001g0347 | 4 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-4780A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845288 | ||||||
chr11:122845330
|
C | T | 40 | a0001c0001t0001g0200a0001c0001t0001g0204a0001c0001t0001g0209others(37): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.47-4738C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845330 | ||||||
chr11:122845333
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.47-4735G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845333 | ||||||
chr11:122845523
|
G | A | 1 | a0005c0008t0001g0236 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47-4545G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845523 | ||||||
chr11:122845610
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-4458G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845610 | ||||||
chr11:122845662
|
A | G | 58 | a0001c0001t0001g0070a0001c0001t0001g0288a0001c0001t0001g0314others(55): Show | 71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-4406A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845662 | ||||||
chr11:122845878
|
C | T | 1 | a0002c0002t0007g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.47-4190C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845878 | ||||||
chr11:122846004
|
C | T | 368 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(365): Show | 426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.47-4064C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846004 | ||||||
chr11:122846020
|
C | A | 1 | a0001c0001t0012g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.47-4048C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846020 | ||||||
chr11:122846073
|
C | T | 1 | a0002c0004t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.47-3995C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846073 | ||||||
chr11:122846107
|
T | C | 3 | a0002c0002t0001g0330a0002c0002t0007g0331a0002c0002t0007g0332 | 3 | HG02647.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.47-3961T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846107 | ||||||
chr11:122846135
|
G | A | 3 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0347 | 5 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-3933G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846135 | ||||||
chr11:122846394
|
C | T | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-3674C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846394 | ||||||
chr11:122846409
|
A | AG | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 301 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.47-3659_47-3658ins others(1): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846409 | ||||||
chr11:122846533
|
C | T | 1 | a0003c0003t0003g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.47-3535C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846533 | ||||||
chr11:122846554
|
A | G | 8 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0005t0001g0219others(5): Show | 10 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-3514A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846554 | ||||||
chr11:122846620
|
CTCTG | C | 30 | a0001c0001t0001g0054a0001c0001t0002g0050a0001c0001t0002g0188others(27): Show | 32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-3428_47-3425del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122846620 | |||||
chr11:122846678
|
C | T | 13 | a0001c0001t0001g0345a0001c0005t0001g0015a0001c0005t0001g0042others(10): Show | 15 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-3390C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846678 | ||||||
chr11:122846802
|
T | A | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-3266T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846802 | ||||||
chr11:122846812
|
T | G | 2 | a0003c0003t0003g0023a0003c0003t0003g0287 | 3 | NA18970.hp1 NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-3256T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846812 | ||||||
chr11:122846897
|
A | C | 1 | a0002c0002t0007g0327 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.47-3171A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846897 | ||||||
chr11:122846910
|
A | G | 1 | a0001c0001t0002g0337 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-3158A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846910 | ||||||
chr11:122847073
|
G | A | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2995G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847073 | ||||||
chr11:122847074
|
A | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2994A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847074 | ||||||
chr11:122847234
|
C | T | 2 | a0002c0002t0001g0339a0002c0002t0007g0062 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.47-2834C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847234 | ||||||
chr11:122847357
|
G | C | 58 | a0001c0001t0001g0247a0001c0001t0001g0288a0001c0001t0001g0314others(55): Show | 71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2711G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847357 | ||||||
chr11:122847387
|
A | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2681A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847387 | ||||||
chr11:122847441
|
T | C | 58 | a0001c0001t0001g0247a0001c0001t0001g0288a0001c0001t0001g0314others(55): Show | 71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2627T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847441 | ||||||
chr11:122847511
|
G | A | 30 | a0001c0001t0001g0054a0001c0001t0002g0050a0001c0001t0002g0188others(27): Show | 32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-2557G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847511 | ||||||
chr11:122847573
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.47-2495C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847573 | ||||||
chr11:122847620
|
A | G | 1 | a0002c0004t0004g0223 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.47-2448A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847620 | ||||||
chr11:122847641
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.47-2427G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847641 | ||||||
chr11:122847982
|
A | T | 58 | a0001c0001t0001g0247a0001c0001t0001g0288a0001c0001t0001g0314others(55): Show | 71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2086A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847982 | ||||||
chr11:122848012
|
G | A | 1 | a0002c0004t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.47-2056G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848012 | ||||||
chr11:122848012
|
G | C | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2056G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848012 | ||||||
chr11:122848013
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2055C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848013 | ||||||
chr11:122848026
|
G | A | 30 | a0001c0001t0001g0054a0001c0001t0002g0050a0001c0001t0002g0188others(27): Show | 32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-2042G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848026 | ||||||
chr11:122848112
|
G | T | 6 | a0002c0002t0001g0178a0002c0002t0001g0286a0002c0002t0009g0185others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-1956G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848112 | ||||||
chr11:122848138
|
T | C | 3 | a0005c0008t0001g0043a0005c0008t0001g0363a0006c0007t0001g0017 | 4 | HG00642.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-1930T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848138 | ||||||
chr11:122848161
|
A | G | 1 | a0002c0002t0006g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.47-1907A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848161 | ||||||
chr11:122848310
|
C | A | 1 | a0002c0002t0006g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-1758C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848310 | ||||||
chr11:122848421
|
A | C | 1 | a0002c0002t0005g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-1647A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848421 | ||||||
chr11:122848538
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.47-1530A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848538 | ||||||
chr11:122848721
|
G | T | 10 | a0001c0001t0001g0345a0001c0005t0001g0015a0001c0005t0001g0042others(7): Show | 12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-1347G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848721 | ||||||
chr11:122848782
|
T | A | 1 | a0003c0003t0003g0280 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.47-1286T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848782 | ||||||
chr11:122848821
|
A | T | 28 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0001g0049others(25): Show | 30 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.47-1247A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848821 | ||||||
chr11:122848878
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0282 | 2 | HG01109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.47-1190T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848878 | ||||||
chr11:122849052
|
G | A | 5 | a0001c0005t0001g0219a0004c0006t0004g0032a0004c0006t0004g0217others(2): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-1016G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849052 | ||||||
chr11:122849154
|
C | T | 2 | a0002c0002t0005g0153a0002c0002t0005g0213 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.47-914C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849154 | ||||||
chr11:122849171
|
C | A | 25 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0002g0050others(22): Show | 27 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.47-897C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849171 | ||||||
chr11:122849284
|
A | G | 1 | a0001c0001t0004g0130 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.47-784A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849284 | ||||||
chr11:122849311
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.47-757G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849311 | ||||||
chr11:122849447
|
T | G | 5 | a0001c0005t0001g0219a0004c0006t0004g0032a0004c0006t0004g0217others(2): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-621T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849447 | ||||||
chr11:122849534
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.47-534C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849534 | ||||||
chr11:122849555
|
C | G | 1 | a0002c0002t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.47-513C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849555 | ||||||
chr11:122849593
|
G | C | 2 | a0002c0004t0004g0197a0002c0004t0004g0198 | 2 | NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.47-475G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849593 | ||||||
chr11:122849613
|
T | C | 14 | a0001c0001t0001g0226a0001c0001t0001g0351a0001c0001t0001g0352others(11): Show | 18 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-455T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849613 | ||||||
chr11:122849707
|
A | T | 2 | a0002c0002t0007g0331a0002c0002t0007g0332 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.47-361A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849707 | ||||||
chr11:122849709
|
T | C | 1 | a0003c0003t0003g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.47-359T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849709 | ||||||
chr11:122849821
|
C | A | 1 | a0002c0002t0005g0199 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.47-247C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849821 | ||||||
chr11:122849824
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.47-244C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849824 | ||||||
chr11:122850002
|
C | T | 26 | a0001c0001t0001g0063a0001c0001t0002g0027a0001c0001t0002g0028others(23): Show | 29 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-66C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122850002 | ||||||
chr11:122850244
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193+30A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850244 | ||||||
chr11:122850287
|
G | A | 2 | a0002c0002t0005g0153a0002c0002t0005g0213 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.193+73G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850287 | ||||||
chr11:122850640
|
A | G | 20 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0002g0210others(17): Show | 22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.193+426A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850640 | ||||||
chr11:122850893
|
A | G | 4 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0219others(1): Show | 6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+679A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850893 | ||||||
chr11:122850988
|
G | A | 2 | a0002c0002t0001g0049a0002c0004t0001g0058 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194-705G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850988 | ||||||
chr11:122851266
|
TA | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(297): Show | 345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.194-410delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 122851266 | |||||
chr11:122851317
|
T | C | 7 | a0001c0001t0001g0345a0002c0002t0005g0153a0002c0002t0005g0213others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-376T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851317 | ||||||
chr11:122851564
|
A | G | 1 | a0002c0002t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.194-129A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851564 | ||||||
chr11:122851592
|
A | T | 31 | a0001c0001t0001g0226a0001c0001t0001g0351a0001c0001t0001g0352others(28): Show | 34 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.194-101A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851592 | ||||||
chr11:122851604
|
C | T | 1 | a0002c0004t0004g0278 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.194-89C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851604 | ||||||
chr11:122851630
|
G | A | 4 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0219others(1): Show | 6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-63G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851630 | ||||||
chr11:122851960
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.346+115G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122851960 | ||||||
chr11:122852076
|
C | T | 2 | a0002c0002t0007g0331a0002c0002t0007g0332 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.346+231C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852076 | ||||||
chr11:122852197
|
G | C | 1 | a0002c0002t0001g0362 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.346+352G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852197 | ||||||
chr11:122852285
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.346+440C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852285 | ||||||
chr11:122852589
|
T | C | 20 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0002g0210others(17): Show | 22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.346+744T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852589 | ||||||
chr11:122852734
|
C | T | 7 | a0001c0001t0001g0345a0002c0002t0005g0153a0002c0002t0005g0213others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+889C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852734 | ||||||
chr11:122852779
|
A | G | 4 | a0008c0013t0011g0232a0008c0013t0011g0234a0008c0013t0011g0235others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+934A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852779 | ||||||
chr11:122852879
|
T | G | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0002g0016 | 5 | HG02071.hp1 NA18950.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1034T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852879 | ||||||
chr11:122852885
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.346+1040C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852885 | ||||||
chr11:122853015
|
C | T | 1 | a0003c0003t0003g0149 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.347-928C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853015 | ||||||
chr11:122853043
|
A | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.347-900A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853043 | ||||||
chr11:122853070
|
C | CT | 82 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0204others(79): Show | 98 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.347-860dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | |||||
chr11:122853070
|
C | CTT | 8 | a0004c0006t0004g0217a0004c0006t0004g0218a0004c0012t0010g0216others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-861_347-860dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | |||||
chr11:122853070
|
C | CTTT | 6 | a0002c0016t0001g0057a0005c0008t0001g0043a0005c0008t0001g0177others(3): Show | 6 | HG00642.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-862_347-860dup others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | |||||
chr11:122853195
|
G | A | 5 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-748G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853195 | ||||||
chr11:122853207
|
A | G | 1 | a0009c0011t0001g0238 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.347-736A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853207 | ||||||
chr11:122853294
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-649T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853294 | ||||||
chr11:122853378
|
C | T | 5 | a0004c0006t0004g0032a0004c0006t0004g0217a0004c0006t0004g0218others(2): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-565C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853378 | ||||||
chr11:122853458
|
C | T | 26 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0002g0050others(23): Show | 28 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-485C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853458 | ||||||
chr11:122853546
|
C | T | 5 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-397C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853546 | ||||||
chr11:122853557
|
A | G | 3 | a0001c0018t0011g0349a0002c0002t0007g0327a0004c0012t0010g0348 | 3 | HG02258.hp1 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-386A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853557 | ||||||
chr11:122853884
|
CT | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.347-56delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853884 | |||||
chr11:122854218
|
G | C | 26 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0002g0050others(23): Show | 28 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+132G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854218 | ||||||
chr11:122854393
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA19077.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.490+307C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854393 | ||||||
chr11:122854471
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.490+385G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854471 | ||||||
chr11:122854486
|
A | G | 9 | a0001c0018t0011g0349a0002c0002t0007g0327a0002c0002t0009g0068others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+400A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854486 | ||||||
chr11:122854516
|
T | TAC | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.490+431_490+432ins others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854516 | |||||
chr11:122854661
|
C | CA | 67 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(64): Show | 73 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.490+589dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854661 | |||||
chr11:122854661
|
C | CAA | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.490+588_490+589dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854661 | |||||
chr11:122854856
|
C | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0002g0050others(28): Show | 34 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.490+770C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854856 | ||||||
chr11:122854865
|
C | T | 1 | a0002c0002t0005g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.490+779C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854865 | ||||||
chr11:122855046
|
C | T | 5 | a0001c0001t0001g0345a0002c0002t0010g0341a0002c0002t0010g0342others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-649C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855046 | ||||||
chr11:122855047
|
G | A | 13 | a0001c0001t0001g0226a0001c0001t0001g0351a0001c0001t0001g0352others(10): Show | 16 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-648G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855047 | ||||||
chr11:122855163
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.491-532C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855163 | ||||||
chr11:122855235
|
C | T | 5 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-460C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855235 | ||||||
chr11:122855275
|
C | T | 3 | a0001c0001t0002g0240a0002c0004t0004g0183a0002c0004t0004g0276 | 3 | HG02257.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.491-420C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855275 | ||||||
chr11:122855407
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-288A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855407 | ||||||
chr11:122855440
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-255A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855440 | ||||||
chr11:122855458
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.491-237T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855458 | ||||||
chr11:122855471
|
A | T | 5 | a0001c0001t0001g0345a0002c0002t0010g0341a0002c0002t0010g0342others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-224A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855471 | ||||||
chr11:122855544
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-151C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855544 | ||||||
chr11:122855545
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-150C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855545 | ||||||
chr11:122855546
|
A | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-149A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855546 | ||||||
chr11:122855550
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-145C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855550 | ||||||
chr11:122855551
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-144C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855551 | ||||||
chr11:122855552
|
A | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-143A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855552 | ||||||
chr11:122855553
|
A | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-142A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855553 | ||||||
chr11:122855554
|
G | A | 1 | a0002c0002t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491-141G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855554 | ||||||
chr11:122855555
|
C | G | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-140C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855555 | ||||||
chr11:122855556
|
C | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-139C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855556 | ||||||
chr11:122855557
|
T | A | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-138T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855557 | ||||||
chr11:122855560
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-135A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855560 | ||||||
chr11:122855561
|
C | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-134C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855561 | ||||||
chr11:122855564
|
G | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-131G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855564 | ||||||
chr11:122855577
|
G | A | 1 | a0001c0001t0001g0346 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.491-118G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855577 | ||||||
chr11:122855623
|
C | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-72C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855623 | ||||||
chr11:122855641
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.491-54C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855641 | ||||||
chr11:122855642
|
C | A | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-53C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855642 | ||||||
chr11:122855644
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-51A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855644 | ||||||
chr11:122855645
|
C | T | 5 | a0005c0010t0007g0228a0005c0010t0007g0237a0005c0010t0015g0230others(2): Show | 5 | HG01109.hp1 HG02630.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-50C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855645 | ||||||
chr11:122855648
|
C | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-47C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855648 | ||||||
chr11:122855657
|
G | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-38G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855657 | ||||||
chr11:122855675
|
C | A | 1 | a0001c0001t0002g0162 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.491-20C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855675 | ||||||
chr11:122855691
|
A | G | 2 | a0002c0002t0007g0331a0002c0002t0007g0332 | 2 | HG02647.hp1 HG02970.hp1 |
splice_region_variant&intron_variant | LOW | c.491-4A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855691 | ||||||
chr11:122855870
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.652+14A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855870 | ||||||
chr11:122855877
|
T | C | 2 | a0002c0002t0007g0062a0002c0002t0007g0227 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.652+21T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855877 | ||||||
chr11:122855955
|
A | T | 1 | a0002c0002t0006g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.652+99A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855955 | ||||||
chr11:122855997
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.652+141C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855997 | ||||||
chr11:122856148
|
G | A | 2 | a0002c0004t0004g0183a0002c0004t0004g0276 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.652+292G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856148 | ||||||
chr11:122856228
|
T | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0163a0001c0001t0002g0181others(1): Show | 5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+372T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856228 | ||||||
chr11:122856361
|
C | T | 41 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0001g0345others(38): Show | 44 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.652+505C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856361 | ||||||
chr11:122856672
|
C | T | 4 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0174others(1): Show | 4 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+816C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856672 | ||||||
chr11:122856869
|
C | T | 93 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0001g0314others(90): Show | 109 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.652+1013C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856869 | ||||||
chr11:122856997
|
C | G | 1 | a0002c0002t0006g0328 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.652+1141C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856997 | ||||||
chr11:122857220
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.652+1364G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857220 | ||||||
chr11:122857232
|
G | A | 13 | a0001c0001t0001g0226a0001c0001t0001g0351a0001c0001t0001g0352others(10): Show | 16 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.652+1376G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857232 | ||||||
chr11:122857244
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 344 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.652+1388A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857244 | ||||||
chr11:122857394
|
G | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0002g0050others(28): Show | 34 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.652+1538G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857394 | ||||||
chr11:122857456
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.652+1600G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857456 | ||||||
chr11:122857464
|
G | A | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.652+1608G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857464 | ||||||
chr11:122857479
|
GAAT | G | 4 | a0005c0010t0007g0237a0005c0010t0015g0230a0009c0011t0001g0229others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+1628_652+1630d others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122857479 | |||||
chr11:122857772
|
G | A | 2 | a0003c0003t0003g0289a0003c0003t0017g0251 | 2 | HG02135.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.652+1916G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857772 | ||||||
chr11:122857946
|
T | C | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.652+2090T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857946 | ||||||
chr11:122858140
|
T | A | 1 | a0003c0003t0003g0290 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.652+2284T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858140 | ||||||
chr11:122858206
|
C | T | 1 | a0002c0002t0006g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.652+2350C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858206 | ||||||
chr11:122858350
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.652+2494G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858350 | ||||||
chr11:122858361
|
G | C | 1 | a0002c0002t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.652+2505G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858361 | ||||||
chr11:122858398
|
A | G | 1 | a0002c0004t0004g0278 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.652+2542A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858398 | ||||||
chr11:122858399
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.652+2543T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858399 | ||||||
chr11:122858440
|
G | GGTCTTGA others(6): Show |
1 | a0001c0001t0002g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.652+2586_652+2598d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122858440 | |||||
chr11:122858560
|
CCTT | C | 11 | a0002c0016t0001g0057a0005c0008t0001g0043a0005c0008t0001g0177others(8): Show | 11 | HG00642.hp2 HG02451.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+2707_652+2709d others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122858560 | |||||
chr11:122858618
|
C | G | 1 | a0005c0008t0014g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652+2762C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858618 | ||||||
chr11:122858693
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.652+2837T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858693 | ||||||
chr11:122858808
|
G | T | 1 | a0003c0003t0003g0315 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.652+2952G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858808 | ||||||
chr11:122858969
|
C | A | 5 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.652+3113C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858969 | ||||||
chr11:122859057
|
G | T | 1 | a0005c0008t0014g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652+3201G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859057 | ||||||
chr11:122859382
|
A | G | 7 | a0002c0002t0007g0327a0002c0002t0009g0068a0002c0002t0009g0150others(4): Show | 7 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-3082A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859382 | ||||||
chr11:122859404
|
T | G | 5 | a0004c0006t0004g0032a0004c0006t0004g0217a0004c0006t0004g0218others(2): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-3060T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859404 | ||||||
chr11:122859431
|
G | GA | 249 | a0001c0001t0001g0012a0001c0001t0001g0054a0001c0001t0001g0063others(246): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.653-3024dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859431 | |||||
chr11:122859431
|
G | GAA | 7 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0219others(4): Show | 9 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.653-3025_653-3024d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859431 | |||||
chr11:122859435
|
A | AC | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.653-3029_653-3028i others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859435 | ||||||
chr11:122859936
|
T | TATCATC | 100 | a0001c0001t0001g0054a0001c0001t0001g0288a0001c0001t0001g0314others(97): Show | 118 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.653-2526_653-2521d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859936 | |||||
chr11:122860011
|
C | T | 1 | a0001c0001t0002g0350 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.653-2453C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860011 | ||||||
chr11:122860046
|
A | C | 4 | a0001c0005t0001g0015a0001c0005t0001g0042a0001c0005t0001g0219others(1): Show | 6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-2418A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860046 | ||||||
chr11:122860092
|
G | C | 2 | a0002c0002t0007g0062a0002c0002t0007g0227 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.653-2372G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860092 | ||||||
chr11:122860153
|
T | C | 5 | a0006c0007t0001g0017a0006c0007t0001g0353a0006c0007t0001g0354others(2): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-2311T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860153 | ||||||
chr11:122860160
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 285 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.653-2304A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860160 | ||||||
chr11:122860273
|
C | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.653-2191C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860273 | ||||||
chr11:122860278
|
G | A | 1 | a0002c0002t0005g0030 | 2 | NA18952.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.653-2186G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860278 | ||||||
chr11:122860454
|
TA | T | 11 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(8): Show | 14 | HG02698.hp1 HG02723.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.653-2009delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860454 | ||||||
chr11:122860633
|
G | A | 44 | a0001c0001t0001g0063a0001c0001t0002g0009a0001c0001t0002g0025others(41): Show | 50 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.653-1831G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860633 | ||||||
chr11:122860684
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.653-1780A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860684 | ||||||
chr11:122860719
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.653-1745T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860719 | ||||||
chr11:122860757
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.653-1707G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860757 | ||||||
chr11:122860772
|
C | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.653-1692C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860772 | ||||||
chr11:122860789
|
G | A | 1 | a0002c0004t0004g0278 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.653-1675G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860789 | ||||||
chr11:122860922
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.653-1542C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860922 | ||||||
chr11:122861023
|
A | G | 1 | a0002c0004t0004g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.653-1441A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861023 | ||||||
chr11:122861024
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.653-1440G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861024 | ||||||
chr11:122861120
|
T | C | 1 | a0002c0004t0004g0255 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.653-1344T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861120 | ||||||
chr11:122861165
|
C | T | 2 | a0002c0002t0007g0331a0002c0002t0007g0332 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.653-1299C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861165 | ||||||
chr11:122861228
|
A | G | 25 | a0001c0001t0001g0226a0001c0001t0001g0351a0001c0001t0001g0352others(22): Show | 30 | HG01167.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.653-1236A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861228 | ||||||
chr11:122861348
|
G | GTA | 11 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG01192.hp2 HG01358.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.653-1103_653-1102d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | |||||
chr11:122861348
|
G | GTATA | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.653-1105_653-1102d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | |||||
chr11:122861348
|
GTA | G | 164 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0204others(161): Show | 186 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.653-1103_653-1102d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | |||||
chr11:122861361
|
T | C | 4 | a0002c0002t0005g0202a0002c0002t0005g0203a0002c0004t0004g0292others(1): Show | 4 | HG00099.hp2 HG02056.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1103T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861361 | ||||||
chr11:122861377
|
T | C | 20 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0018t0011g0349others(17): Show | 22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.653-1087T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861377 | ||||||
chr11:122861386
|
GTATATA | G | 4 | a0002c0002t0005g0153a0002c0002t0005g0213a0002c0002t0007g0359others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1048_653-1043d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(3): Show |
G | 4 | a0001c0001t0001g0074a0001c0001t0001g0122a0002c0002t0007g0332others(1): Show | 4 | HG02970.hp1 HG03540.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1052_653-1043d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(5): Show |
G | 3 | a0001c0001t0001g0103a0001c0001t0001g0226a0001c0001t0002g0104 | 3 | HG00673.hp2 HG01884.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.653-1054_653-1043d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(7): Show |
G | 1 | a0005c0010t0007g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653-1056_653-1043d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(11): Show |
G | 10 | a0001c0001t0001g0209a0002c0002t0005g0030a0002c0002t0005g0031others(7): Show | 12 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.653-1060_653-1043d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(13): Show |
G | 1 | a0002c0004t0004g0274 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.653-1062_653-1043d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861386
|
GTATATAT others(15): Show |
G | 1 | a0002c0004t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.653-1064_653-1043d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | |||||
chr11:122861400
|
ATATATAT others(24): Show |
A | 5 | a0001c0001t0001g0054a0001c0001t0002g0050a0002c0002t0006g0053others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1062_653-1032d others(33): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | |||||
chr11:122861400
|
ATATATAT others(25): Show |
A | 19 | a0001c0001t0001g0288a0002c0002t0001g0049a0002c0002t0001g0362others(16): Show | 21 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.653-1062_653-1031d others(34): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | |||||
chr11:122861400
|
ATATATAT others(26): Show |
A | 1 | a0002c0002t0006g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.653-1062_653-1030d others(35): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | |||||
chr11:122861401
|
TATATATA others(10): Show |
T | 1 | a0002c0002t0005g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.653-1062_653-1046d others(19): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861401 | ||||||
chr11:122861401
|
TATATATA others(12): Show |
T | 1 | a0002c0002t0005g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.653-1062_653-1044d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861401 | ||||||
chr11:122861402
|
ATATATAT others(12): Show |
A | 1 | a0002c0002t0007g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.653-1060_653-1042d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | |||||
chr11:122861402
|
ATATATAT others(13): Show |
A | 1 | a0002c0002t0007g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.653-1060_653-1041d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | |||||
chr11:122861402
|
ATATATAT others(16): Show |
A | 2 | a0005c0010t0015g0230a0009c0011t0001g0231 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.653-1060_653-1038d others(25): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | |||||
chr11:122861402
|
ATATATAT others(17): Show |
A | 1 | a0005c0010t0007g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.653-1060_653-1037d others(26): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | |||||
chr11:122861402
|
ATATATAT others(24): Show |
A | 1 | a0002c0002t0006g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.653-1060_653-1030d others(33): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | |||||
chr11:122861404
|
ATATATAT others(12): Show |
A | 2 | a0003c0003t0003g0073a0003c0003t0003g0289 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.653-1058_653-1040d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | |||||
chr11:122861404
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0002g0313a0003c0003t0003g0326 | 2 | NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.653-1058_653-1038d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | |||||
chr11:122861404
|
ATATATAT others(15): Show |
A | 1 | a0003c0003t0003g0312 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.653-1058_653-1037d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | |||||
chr11:122861405
|
TATATATA others(6): Show |
T | 1 | a0002c0004t0004g0273 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.653-1058_653-1046d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861405 | ||||||
chr11:122861406
|
ATATATAT others(11): Show |
A | 3 | a0002c0004t0003g0284a0003c0003t0003g0040a0003c0003t0003g0311 | 4 | HG03098.hp1 NA18992.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1056_653-1039d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | |||||
chr11:122861406
|
ATATATAT others(12): Show |
A | 30 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0321others(27): Show | 41 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.653-1056_653-1038d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | |||||
chr11:122861406
|
ATATATAT others(13): Show |
A | 8 | a0003c0003t0003g0146a0003c0003t0003g0280a0003c0003t0003g0290others(5): Show | 8 | HG00544.hp1 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-1056_653-1037d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | |||||
chr11:122861407
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0128 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.653-1056_653-1044d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861407 | ||||||
chr11:122861408
|
ATATATAT others(6): Show |
A | 14 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0083others(11): Show | 16 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.653-1054_653-1042d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(7): Show |
A | 6 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0002g0099others(3): Show | 6 | HG00280.hp1 HG00609.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-1054_653-1041d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(8): Show |
A | 3 | a0001c0001t0002g0060a0001c0001t0002g0162a0001c0001t0002g0188 | 3 | HG01123.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.653-1054_653-1040d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0002g0059 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.653-1054_653-1039d others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0314a0003c0003t0003g0038a0003c0003t0003g0140others(3): Show | 7 | HG00735.hp1 HG01261.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.653-1054_653-1037d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(12): Show |
A | 5 | a0003c0003t0003g0293a0003c0003t0003g0319a0003c0003t0003g0320others(2): Show | 5 | HG03669.hp1 NA18946.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1054_653-1036d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(13): Show |
A | 1 | a0002c0002t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653-1054_653-1035d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861408
|
ATATATAT others(14): Show |
A | 1 | a0002c0002t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.653-1054_653-1034d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | |||||
chr11:122861409
|
TATATATA others(4): Show |
T | 3 | a0005c0008t0001g0177a0005c0008t0014g0285a0005c0015t0004g0045 | 3 | HG02895.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.653-1054_653-1044d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861409 | ||||||
chr11:122861410
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0118others(2): Show | 6 | HG00408.hp1 HG03471.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-1052_653-1042d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861410
|
ATATATAT others(5): Show |
A | 12 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0082others(9): Show | 14 | HG00423.hp2 HG01346.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.653-1052_653-1041d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861410
|
ATATATAT others(6): Show |
A | 33 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0024others(30): Show | 39 | HG00438.hp2 HG00735.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.653-1052_653-1040d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861410
|
ATATATAT others(7): Show |
A | 24 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0027others(21): Show | 28 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.653-1052_653-1039d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861410
|
ATATATAT others(8): Show |
A | 7 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0112others(4): Show | 7 | HG00140.hp1 HG01516.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-1052_653-1038d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861410
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.653-1052_653-1032d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | |||||
chr11:122861412
|
ATATATAT others(3): Show |
A | 2 | a0002c0016t0001g0057a0005c0008t0001g0363 | 2 | HG00642.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.653-1050_653-1041d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0087a0010c0020t0005g0233 | 2 | HG02451.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.653-1050_653-1040d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0008g0002a0001c0001t0008g0086 | 5 | HG00738.hp1 HG01258.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1050_653-1039d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(6): Show |
A | 13 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0044others(10): Show | 18 | HG01243.hp2 HG01256.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.653-1050_653-1038d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0123a0001c0001t0002g0166 | 2 | HG02698.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.653-1050_653-1037d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(8): Show |
A | 5 | a0001c0001t0002g0165a0001c0005t0001g0015a0001c0005t0001g0219others(2): Show | 7 | HG01109.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.653-1050_653-1036d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(9): Show |
A | 1 | a0001c0005t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653-1050_653-1035d others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(10): Show |
A | 1 | a0002c0002t0010g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.653-1050_653-1034d others(19): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(13): Show |
A | 5 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1050_653-1031d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861412
|
ATATATAT others(15): Show |
A | 1 | a0008c0013t0011g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.653-1050_653-1029d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | |||||
chr11:122861414
|
ATATATAT others(3): Show |
A | 1 | a0007c0009t0003g0061 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.653-1048_653-1039d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861414 | |||||
chr11:122861414
|
ATATATAT others(11): Show |
A | 1 | a0002c0002t0009g0338 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.653-1048_653-1031d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861414 | |||||
chr11:122861416
|
A | T | 3 | a0002c0002t0005g0153a0002c0002t0005g0206a0002c0002t0005g0213 | 3 | HG02615.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.653-1048A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861416 | ||||||
chr11:122861416
|
ATATATTT others(4): Show |
A | 1 | a0002c0004t0001g0357 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.653-1046_653-1036d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861416 | |||||
chr11:122861418
|
A | AT | 15 | a0001c0001t0001g0248a0001c0001t0001g0317a0001c0001t0002g0077others(12): Show | 16 | HG01106.hp2 HG01261.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.653-1045dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | |||||
chr11:122861418
|
A | ATTT | 3 | a0001c0001t0002g0252a0001c0018t0011g0349a0002c0004t0004g0270 | 3 | HG02738.hp1 HG03209.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.653-1045_653-1044i others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | |||||
chr11:122861418
|
A | T | 13 | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0002g0275others(10): Show | 13 | HG01192.hp2 HG01361.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.653-1046A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861418 | ||||||
chr11:122861418
|
ATATTTTT others(3): Show |
A | 2 | a0004c0006t0004g0032a0004c0006t0004g0218 | 3 | HG01891.hp1 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653-1044_653-1035d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | |||||
chr11:122861418
|
ATATTTTT others(4): Show |
A | 1 | a0004c0012t0009g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.653-1044_653-1034d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | |||||
chr11:122861420
|
A | ATATATAT others(6): Show |
1 | a0002c0004t0004g0256 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.653-1043_653-1042i others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | |||||
chr11:122861420
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0006g0328 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.653-1043_653-1042i others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | |||||
chr11:122861420
|
A | ATT | 10 | a0001c0001t0001g0260a0001c0001t0002g0138a0001c0001t0002g0243others(7): Show | 10 | HG01099.hp1 HG02074.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.653-1015_653-1014d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | |||||
chr11:122861420
|
A | T | 51 | a0001c0001t0001g0209a0001c0001t0001g0248a0001c0001t0001g0317others(48): Show | 58 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.653-1044A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861420 | ||||||
chr11:122861422
|
T | A | 2 | a0002c0004t0003g0034a0002c0004t0004g0292 | 3 | HG00099.hp2 NA18942.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.653-1042T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861422 | ||||||
chr11:122861422
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653-1042T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861422 | ||||||
chr11:122861423
|
T | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG03130.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.653-1041T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861423 | ||||||
chr11:122861426
|
T | A | 2 | a0001c0001t0002g0350a0006c0007t0001g0353 | 2 | HG02818.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.653-1038T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861426 | ||||||
chr11:122861451
|
G | T | 1 | a0002c0002t0005g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.653-1013G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861451 | ||||||
chr11:122861470
|
C | T | 2 | a0002c0002t0009g0185a0002c0002t0010g0184 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.653-994C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861470 | ||||||
chr11:122861475
|
G | A | 6 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-989G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861475 | ||||||
chr11:122861538
|
C | T | 20 | a0001c0001t0001g0288a0002c0002t0001g0049a0002c0002t0001g0362others(17): Show | 22 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.653-926C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861538 | ||||||
chr11:122861592
|
A | G | 1 | a0002c0004t0004g0134 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.653-872A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861592 | ||||||
chr11:122861596
|
C | T | 22 | a0001c0001t0001g0054a0001c0001t0001g0204a0001c0001t0001g0209others(19): Show | 24 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.653-868C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861596 | ||||||
chr11:122861600
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.653-864C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861600 | ||||||
chr11:122861895
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.653-569T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861895 | ||||||
chr11:122861989
|
G | T | 6 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-475G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861989 | ||||||
chr11:122862004
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.653-460A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862004 | ||||||
chr11:122862019
|
G | GA | 43 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(40): Show | 49 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.653-437dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122862019 | |||||
chr11:122862045
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.653-419T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862045 | ||||||
chr11:122862087
|
T | C | 2 | a0001c0018t0011g0349a0004c0012t0010g0348 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.653-377T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862087 | ||||||
chr11:122862164
|
G | T | 48 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(45): Show | 54 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.653-300G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862164 | ||||||
chr11:122862167
|
A | T | 1 | a0002c0002t0006g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.653-297A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862167 | ||||||
chr11:122862191
|
A | G | 2 | a0002c0002t0007g0359a0002c0002t0007g0360 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.653-273A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862191 | ||||||
chr11:122862275
|
A | C | 1 | a0002c0002t0005g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.653-189A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862275 | ||||||
chr11:122862372
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653-92C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862372 | ||||||
chr11:122862721
|
G | A | 5 | a0004c0006t0004g0032a0004c0006t0004g0217a0004c0006t0004g0218others(2): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+177G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862721 | ||||||
chr11:122862816
|
C | A | 1 | a0002c0004t0004g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.733+272C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862816 | ||||||
chr11:122862894
|
TG | T | 54 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(51): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.733+351delG | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862894 | ||||||
chr11:122862937
|
G | T | 1 | a0005c0010t0007g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733+393G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862937 | ||||||
chr11:122862941
|
C | T | 1 | a0002c0004t0004g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.733+397C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862941 | ||||||
chr11:122862950
|
G | C | 5 | a0001c0001t0002g0016a0001c0001t0002g0215a0001c0001t0002g0309others(2): Show | 7 | HG02071.hp1 HG03831.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+406G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862950 | ||||||
chr11:122863109
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.733+565A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863109 | ||||||
chr11:122863228
|
C | CGAAA | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.733+703_733+706dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | |||||
chr11:122863228
|
C | CGAAAGAA others(5): Show |
2 | a0002c0002t0007g0332a0002c0002t0007g0359 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.733+695_733+706dup others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | |||||
chr11:122863228
|
C | CGAAAGAA others(9): Show |
1 | a0002c0002t0007g0331 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.733+691_733+706dup others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | |||||
chr11:122863247
|
A | G | 4 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+703A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863247 | ||||||
chr11:122863251
|
G | A | 5 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+707G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863251 | ||||||
chr11:122863255
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0139 | 4 | NA18973.hp2 NA19000.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+711A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863255 | ||||||
chr11:122863257
|
G | A | 5 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+713G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863257 | ||||||
chr11:122863258
|
A | G | 4 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+714A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863258 | ||||||
chr11:122863262
|
GAAAGAAA others(3): Show |
G | 50 | a0001c0001t0002g0313a0003c0003t0003g0004a0003c0003t0003g0005others(47): Show | 63 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.733+730_733+739del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863262 | |||||
chr11:122863264
|
A | G | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+720A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863264 | ||||||
chr11:122863270
|
G | A | 4 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+726G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863270 | ||||||
chr11:122863272
|
A | AAAAG | 284 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.733+740_733+743dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863272 | |||||
chr11:122863272
|
A | G | 4 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+728A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863272 | ||||||
chr11:122863288
|
A | G | 7 | a0001c0001t0002g0077a0002c0002t0006g0196a0002c0002t0006g0328others(4): Show | 7 | HG01934.hp1 HG02630.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+744A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863288 | ||||||
chr11:122863290
|
G | A | 6 | a0001c0001t0002g0077a0002c0002t0006g0196a0002c0002t0006g0328others(3): Show | 6 | HG01934.hp1 HG02630.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+746G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863290 | ||||||
chr11:122863290
|
G | T | 2 | a0003c0003t0003g0148a0003c0003t0003g0308 | 2 | HG00673.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.733+746G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863290 | ||||||
chr11:122863300
|
G | A | 6 | a0002c0002t0006g0328a0002c0004t0003g0284a0005c0010t0007g0228others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+756G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863300 | ||||||
chr11:122863304
|
A | G | 4 | a0002c0002t0006g0328a0005c0010t0007g0237a0005c0010t0015g0230others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+760A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863304 | ||||||
chr11:122863306
|
GAAAAGAA others(8): Show |
G | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+766_733+780del others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863306 | |||||
chr11:122863310
|
A | G | 4 | a0002c0002t0006g0328a0005c0010t0007g0237a0005c0010t0015g0230others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+766A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863310 | ||||||
chr11:122863311
|
G | A | 4 | a0002c0002t0006g0328a0005c0010t0007g0237a0005c0010t0015g0230others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+767G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863311 | ||||||
chr11:122863311
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0002g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.733+779_733+788del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863311 | |||||
chr11:122863313
|
A | G | 1 | a0002c0002t0006g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.733+769A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863313 | ||||||
chr11:122863321
|
A | AAAAG | 22 | a0001c0001t0001g0087a0001c0001t0001g0129a0001c0001t0001g0142others(19): Show | 23 | HG00609.hp2 HG01106.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.733+805_733+808dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | |||||
chr11:122863321
|
A | AAAAGAAA others(1): Show |
3 | a0001c0001t0002g0111a0001c0001t0002g0340a0001c0001t0008g0096 | 3 | HG01496.hp1 HG01943.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.733+801_733+808dup others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | |||||
chr11:122863321
|
A | AAAAGAAA others(5): Show |
1 | a0001c0001t0002g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.733+797_733+808dup others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | |||||
chr11:122863321
|
AAAAG | A | 19 | a0001c0001t0001g0097a0002c0002t0001g0330a0002c0002t0001g0339others(16): Show | 19 | HG00642.hp2 HG02615.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.733+805_733+808del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | |||||
chr11:122863321
|
AAAAGAAA others(1): Show |
A | 51 | a0001c0001t0002g0313a0002c0002t0007g0332a0003c0003t0003g0004others(48): Show | 64 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.733+801_733+808del others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | |||||
chr11:122863322
|
AAAGAAAG others(8): Show |
A | 4 | a0002c0002t0010g0341a0002c0002t0010g0342a0002c0002t0010g0343others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+781_733+795del others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863322 | |||||
chr11:122863325
|
GAAAGAA | G | 3 | a0005c0010t0007g0237a0005c0010t0015g0230a0009c0011t0001g0231 | 3 | HG02630.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.733+783_733+788del others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863325 | |||||
chr11:122863329
|
GAAAGAAA others(15): Show |
G | 1 | a0001c0001t0002g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.733+805_733+826del others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863329 | |||||
chr11:122863333
|
GAAAGAAA others(11): Show |
G | 2 | a0001c0001t0002g0167a0007c0009t0003g0262 | 2 | HG00140.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+826_733+843del others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863333 | |||||
chr11:122863337
|
GAAAGAAA others(7): Show |
G | 21 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(18): Show | 25 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.733+809_733+822del others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863337 | |||||
chr11:122863341
|
GAAAGAAA others(3): Show |
G | 13 | a0001c0001t0002g0028a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 14 | HG00639.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.733+809_733+818del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863341 | |||||
chr11:122863343
|
AAGAAAGA others(5): Show |
A | 1 | a0002c0004t0004g0255 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.733+801_733+812del others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863343 | |||||
chr11:122863345
|
GAAAGAA | G | 4 | a0001c0001t0002g0060a0001c0001t0002g0162a0001c0001t0002g0166others(1): Show | 4 | HG01123.hp1 HG02698.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+809_733+814del others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863345 | |||||
chr11:122863347
|
AAGAAAAA others(1): Show |
A | 58 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0002g0022others(55): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.733+805_733+812del others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863347 | |||||
chr11:122863349
|
G | A | 2 | a0002c0004t0003g0284a0010c0020t0005g0233 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.733+805G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863349 | ||||||
chr11:122863349
|
GAA | G | 8 | a0001c0001t0002g0059a0001c0001t0002g0175a0001c0001t0007g0164others(5): Show | 8 | HG01070.hp2 HG01175.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+809_733+810del others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863349 | |||||
chr11:122863351
|
A | AAG | 3 | a0001c0001t0002g0029a0002c0002t0005g0283a0002c0004t0004g0256 | 4 | HG01069.hp2 HG01175.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+808_733+809ins others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | |||||
chr11:122863351
|
A | AAGAAAGA others(3): Show |
1 | a0002c0002t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.733+808_733+809ins others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | |||||
chr11:122863351
|
A | AAGAAAGA others(19): Show |
1 | a0002c0002t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.733+808_733+809ins others(26): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | |||||
chr11:122863351
|
A | G | 3 | a0002c0004t0003g0284a0005c0010t0007g0228a0010c0020t0005g0233 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.733+807A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863351 | ||||||
chr11:122863351
|
AAAAG | A | 28 | a0001c0001t0001g0345a0001c0001t0002g0077a0001c0001t0002g0265others(25): Show | 30 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.733+823_733+826del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | |||||
chr11:122863353
|
A | G | 1 | a0002c0002t0006g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733+809A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863353 | ||||||
chr11:122863355
|
G | A | 1 | a0002c0002t0006g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733+811G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863355 | ||||||
chr11:122863477
|
A | G | 1 | a0009c0011t0001g0229 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.733+933A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863477 | ||||||
chr11:122863603
|
C | A | 1 | a0002c0002t0006g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.734-1033C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863603 | ||||||
chr11:122863626
|
GTACCA | G | 6 | a0002c0002t0001g0330a0002c0002t0001g0339a0002c0002t0005g0153others(3): Show | 6 | HG02615.hp1 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-1006_734-1002d others(7): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863626 | |||||
chr11:122863791
|
A | G | 2 | a0002c0004t0004g0003a0002c0004t0004g0105 | 5 | HG01070.hp1 HG01071.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-845A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863791 | ||||||
chr11:122864000
|
C | A | 1 | a0007c0009t0013g0158 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.734-636C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122864000 | ||||||
chr11:122864166
|
C | T | 1 | a0005c0008t0014g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.734-470C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122864166 | ||||||
chr11:122864794
|
G | A | 9 | a0002c0002t0001g0178a0002c0002t0009g0068a0002c0002t0009g0150others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.817+75G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864794 | ||||||
chr11:122864850
|
T | C | 14 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(11): Show | 17 | HG02698.hp1 HG03831.hp2 HG03834.hp2 others(14): Show |
intron_variant | MODIFIER | c.817+131T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864850 | ||||||
chr11:122864925
|
C | T | 1 | a0001c0018t0011g0349 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.817+206C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864925 | ||||||
chr11:122865031
|
T | A | 1 | a0001c0001t0002g0350 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817+312T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865031 | ||||||
chr11:122865045
|
T | A | 19 | a0002c0002t0001g0362a0002c0002t0006g0010a0002c0002t0006g0051others(16): Show | 21 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.817+326T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865045 | ||||||
chr11:122865101
|
A | G | 3 | a0002c0002t0006g0195a0002c0002t0006g0196a0002c0002t0006g0366 | 3 | HG01081.hp2 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.817+382A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865101 | ||||||
chr11:122865188
|
C | G | 3 | a0001c0001t0001g0019a0007c0009t0003g0019a0007c0009t0003g0061 | 3 | HG00408.hp2 NA18961.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.817+469C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865188 | ||||||
chr11:122865241
|
G | T | 8 | a0002c0002t0009g0068a0002c0002t0009g0150a0002c0002t0009g0151others(5): Show | 8 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.817+522G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865241 | ||||||
chr11:122865325
|
G | A | 1 | a0002c0002t0009g0150 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.817+606G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865325 | ||||||
chr11:122865408
|
CT | C | 76 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0022others(73): Show | 86 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.817+690delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865408 | ||||||
chr11:122865454
|
T | C | 3 | a0003c0003t0003g0300a0003c0003t0003g0301a0003c0003t0003g0302 | 3 | NA18956.hp2 NA18974.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.817+735T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865454 | ||||||
chr11:122865499
|
G | A | 86 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0022others(83): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.817+780G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865499 | ||||||
chr11:122865514
|
A | T | 349 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(346): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.817+795A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865514 | ||||||
chr11:122865562
|
A | G | 61 | a0002c0002t0001g0049a0002c0002t0001g0178a0002c0002t0001g0330others(58): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.817+843A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865562 | ||||||
chr11:122865569
|
A | T | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817+850A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865569 | ||||||
chr11:122865580
|
C | T | 1 | a0002c0002t0005g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817+861C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865580 | ||||||
chr11:122865717
|
C | G | 2 | a0002c0002t0005g0153a0002c0002t0005g0213 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.817+998C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865717 | ||||||
chr11:122865718
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.817+999A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865718 | ||||||
chr11:122865738
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.817+1019C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865738 | ||||||
chr11:122865849
|
T | G | 4 | a0001c0001t0002g0252a0001c0001t0002g0257a0001c0001t0002g0266others(1): Show | 4 | HG01106.hp2 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+1130T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865849 | ||||||
chr11:122865863
|
C | T | 86 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0022others(83): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.817+1144C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865863 | ||||||
chr11:122865892
|
C | G | 6 | a0002c0002t0001g0362a0002c0016t0001g0057a0005c0008t0001g0043others(3): Show | 6 | HG00642.hp2 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+1173C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865892 | ||||||
chr11:122866145
|
A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.818-1264A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866145 | ||||||
chr11:122866520
|
CCTT | C | 4 | a0001c0001t0002g0016a0001c0001t0002g0309a0001c0001t0002g0310others(1): Show | 6 | HG02071.hp1 NA18945.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.818-888_818-886del others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866520 | ||||||
chr11:122866607
|
CT | C | 84 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0022others(81): Show | 94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.818-787delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122866607 | |||||
chr11:122866769
|
A | G | 1 | a0002c0002t0006g0194 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.818-640A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866769 | ||||||
chr11:122866774
|
T | A | 29 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0033others(26): Show | 33 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.818-635T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866774 | ||||||
chr11:122866919
|
T | C | 1 | a0002c0004t0003g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.818-490T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866919 | ||||||
chr11:122866997
|
A | G | 50 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0013others(47): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.818-412A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866997 | ||||||
chr11:122867025
|
T | C | 1 | a0002c0002t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.818-384T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867025 | ||||||
chr11:122867057
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.818-352T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867057 | ||||||
chr11:122867102
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.818-307C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867102 | ||||||
chr11:122867225
|
G | C | 2 | a0002c0002t0001g0178a0002c0002t0001g0339 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.818-184G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867225 | ||||||
chr11:122867324
|
GT | G | 8 | a0002c0002t0005g0283a0002c0002t0010g0184a0002c0002t0010g0341others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.818-84delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867324 | ||||||
chr11:122867354
|
CA | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0090others(24): Show | 29 | HG00423.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.818-39delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | |||||
chr11:122867354
|
CAA | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(305): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.818-40_818-39delAA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | |||||
chr11:122867354
|
CAAA | C | 16 | a0001c0001t0002g0259a0002c0002t0001g0049a0002c0002t0001g0178others(13): Show | 17 | HG00642.hp2 HG00741.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.818-41_818-39delAA others(1): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | |||||
chr11:122867592
|
G | A | 6 | a0002c0002t0001g0362a0002c0016t0001g0057a0005c0008t0001g0043others(3): Show | 6 | HG00642.hp2 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+37G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122867592 | ||||||
chr11:122867739
|
C | T | 1 | a0001c0005t0001g0219 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.964+184C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122867739 | ||||||
chr11:122868010
|
T | C | 49 | a0002c0004t0003g0034a0002c0004t0003g0284a0002c0004t0004g0003others(46): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
splice_region_variant&intron_variant | LOW | c.965-3T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122868010 | ||||||
chr11:122868188
|
A | ATG | 28 | a0001c0001t0002g0033a0001c0001t0002g0111a0001c0001t0002g0133others(25): Show | 29 | HG00621.hp2 HG00741.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.1051+137_1051+138d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTG | 21 | a0001c0001t0002g0016a0001c0001t0002g0136a0001c0001t0002g0138others(18): Show | 25 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1051+135_1051+138d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTGTG | 13 | a0001c0001t0002g0077a0001c0001t0002g0137a0001c0001t0002g0257others(10): Show | 13 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1051+133_1051+138d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0002g0253a0002c0002t0001g0178a0002c0002t0001g0339others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+131_1051+138d others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTGTGT others(3): Show |
7 | a0001c0001t0002g0254a0001c0001t0002g0258a0001c0001t0002g0266others(4): Show | 7 | HG01106.hp2 HG01168.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051+129_1051+138d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0224a0011c0019t0009g0176 | 2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1051+127_1051+138d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1051+125_1051+138d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
A | G | 1 | a0001c0001t0002g0321 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1051+89A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868188 | ||||||
chr11:122868188
|
ATG | A | 43 | a0001c0001t0001g0142a0001c0001t0001g0345a0001c0001t0002g0025others(40): Show | 49 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.1051+137_1051+138d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTG | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0114others(69): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1051+135_1051+138d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTGTG | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0075others(32): Show | 43 | HG00558.hp2 HG01099.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1051+133_1051+138d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTGTGT others(1): Show |
A | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0012others(56): Show | 72 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1051+131_1051+138d others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTGTGT others(3): Show |
A | 25 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0067others(22): Show | 30 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1051+129_1051+138d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0113a0009c0011t0001g0238 | 2 | HG01257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1051+127_1051+138d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868188
|
ATGTGTGT others(7): Show |
A | 1 | a0003c0003t0003g0326 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1051+125_1051+138d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | |||||
chr11:122868247
|
G | A | 4 | a0002c0002t0001g0049a0002c0002t0001g0178a0002c0002t0001g0330others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+148G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868247 | ||||||
chr11:122868866
|
G | A | 3 | a0002c0016t0001g0057a0005c0008t0001g0043a0005c0008t0001g0363 | 3 | HG00642.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1051+767G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868866 | ||||||
chr11:122868928
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1051+829G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868928 | ||||||
chr11:122868933
|
C | T | 1 | a0002c0002t0006g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1051+834C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868933 | ||||||
chr11:122868958
|
G | A | 7 | a0002c0002t0007g0062a0002c0002t0007g0227a0002c0002t0007g0327others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+859G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868958 | ||||||
chr11:122868967
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1051+868C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868967 | ||||||
chr11:122869009
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1051+910A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869009 | ||||||
chr11:122869051
|
C | A | 1 | a0002c0002t0005g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1051+952C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869051 | ||||||
chr11:122869375
|
A | C | 20 | a0002c0002t0006g0010a0002c0002t0006g0051a0002c0002t0006g0052others(17): Show | 22 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+1276A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869375 | ||||||
chr11:122869387
|
A | G | 51 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0013others(48): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1051+1288A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869387 | ||||||
chr11:122869493
|
G | A | 3 | a0002c0002t0006g0190a0002c0002t0006g0193a0002c0002t0006g0194 | 3 | HG02602.hp2 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1051+1394G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869493 | ||||||
chr11:122869552
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1051+1453A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869552 | ||||||
chr11:122869704
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1052-1565G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869704 | ||||||
chr11:122869820
|
T | C | 5 | a0003c0003t0003g0089a0003c0003t0003g0296a0003c0003t0003g0298others(2): Show | 5 | HG00544.hp1 NA18957.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1449T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869820 | ||||||
chr11:122869838
|
G | C | 12 | a0002c0002t0001g0049a0002c0002t0001g0178a0002c0002t0001g0286others(9): Show | 12 | HG00642.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052-1431G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869838 | ||||||
chr11:122870005
|
C | T | 1 | a0002c0016t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1052-1264C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870005 | ||||||
chr11:122870149
|
T | C | 2 | a0005c0010t0007g0237a0005c0010t0015g0230 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1052-1120T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870149 | ||||||
chr11:122870152
|
G | T | 12 | a0002c0002t0001g0049a0002c0002t0001g0178a0002c0002t0001g0286others(9): Show | 12 | HG00642.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052-1117G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870152 | ||||||
chr11:122870173
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1052-1096C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870173 | ||||||
chr11:122870174
|
G | A | 1 | a0002c0004t0004g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1052-1095G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870174 | ||||||
chr11:122870187
|
C | T | 5 | a0002c0002t0007g0062a0002c0002t0007g0227a0002c0002t0007g0327others(2): Show | 5 | HG02922.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-1082C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870187 | ||||||
chr11:122870219
|
T | C | 7 | a0002c0002t0007g0062a0002c0002t0007g0227a0002c0002t0007g0327others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052-1050T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870219 | ||||||
chr11:122870229
|
C | T | 1 | a0003c0003t0003g0304 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1052-1040C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870229 | ||||||
chr11:122870291
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0016g0169 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1052-978G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870291 | ||||||
chr11:122870307
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1052-962C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870307 | ||||||
chr11:122870515
|
G | A | 1 | a0002c0002t0005g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1052-754G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870515 | ||||||
chr11:122870628
|
C | A | 2 | a0002c0002t0001g0049a0002c0002t0001g0330 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1052-641C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870628 | ||||||
chr11:122870672
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1052-597A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870672 | ||||||
chr11:122871057
|
T | A | 1 | a0001c0001t0008g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1052-212T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122871057 | ||||||
chr11:122871092
|
G | A | 31 | a0001c0001t0007g0164a0002c0002t0006g0010a0002c0002t0006g0051others(28): Show | 33 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1052-177G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122871092 |