geneid | 10491 |
---|---|
ensemblid | ENSG00000170275.15 |
hgncid | 2379 |
symbol | CRTAP |
name | cartilage associated protein |
refseq_nuc | NM_006371.5 |
refseq_prot | NP_006362.1 |
ensembl_nuc | ENST00000320954.11 |
ensembl_prot | ENSP00000323696.5 |
mane_status | MANE Select |
chr | chr3 |
start | 33114014 |
end | 33147773 |
strand | + |
ver | v1.2 |
region | chr3:33114014-33147773 |
region5000 | chr3:33109014-33152773 |
regionname0 | CRTAP_chr3_33114014_33147773 |
regionname5000 | CRTAP_chr3_33109014_33152773 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 401 | 401 | 87 | 78 | 177 | 12 | 45 | 135 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0002 | 0/0 | 401 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0003 | 0/0 | 401 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0004 | 0/0 | 401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0005 | 0/0 | 401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1206 | 155 | 23 | 46 | 57 | 7 | 20 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0002 | 0/0 | 1206 | 107 | 12 | 5 | 81 | 1 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0003 | 0/0 | 1206 | 84 | 17 | 21 | 26 | 4 | 16 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0004 | 0/0 | 1206 | 24 | 12 | 2 | 9 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0005 | 0/0 | 1206 | 11 | 11 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0006 | 0/0 | 1206 | 11 | 6 | 1 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0007 | 0/0 | 1206 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0008 | 0/0 | 1206 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0009 | 0/0 | 1206 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0010 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0011 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0012 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0013 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0014 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0015 | 0/0 | 1206 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
c0016 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5390 | 84 | 4 | 10 | 58 | 0 | 12 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0002 | 0/0 | 5396 | 73 | 12 | 27 | 19 | 6 | 9 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0003 | 0/0 | 5390 | 64 | 3 | 11 | 38 | 1 | 11 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0004 | 0/0 | 5390 | 18 | 0 | 8 | 10 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0005 | 0/0 | 5389 | 17 | 10 | 1 | 6 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0006 | 0/0 | 5390 | 9 | 5 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0007 | 0/0 | 5390 | 8 | 8 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0008 | 0/0 | 5391 | 8 | 5 | 3 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0009 | 0/0 | 5390 | 8 | 0 | 0 | 7 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0010 | 0/0 | 5390 | 6 | 0 | 3 | 0 | 2 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0011 | 0/0 | 5390 | 5 | 0 | 0 | 5 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0012 | 0/0 | 5391 | 4 | 0 | 1 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0013 | 0/0 | 5390 | 4 | 1 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0014 | 0/0 | 5396 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0015 | 0/0 | 5396 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0016 | 0/0 | 5396 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0017 | 0/0 | 5389 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0018 | 0/0 | 5389 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0019 | 0/0 | 5390 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0020 | 0/0 | 5396 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0021 | 0/0 | 5397 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0022 | 0/0 | 5396 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0023 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0024 | 0/0 | 5396 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0025 | 0/0 | 5389 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0026 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0027 | 0/0 | 5390 | 2 | 0 | 0 | 1 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0028 | 0/0 | 5389 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0029 | 0/1 | 5390 | 2 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0030 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0031 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0032 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0033 | 0/0 | 5390 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0034 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0035 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0036 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0037 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0038 | 0/0 | 5395 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0039 | 0/0 | 5396 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0040 | 0/0 | 5396 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0041 | 0/0 | 5396 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0042 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0043 | 0/0 | 5396 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0044 | 0/0 | 5396 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0045 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0046 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0047 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0048 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0049 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0050 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0051 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0052 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0053 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0054 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0055 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0056 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0057 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0058 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0059 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0060 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0061 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0062 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0063 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0064 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0065 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0066 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0067 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0068 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0069 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0070 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0071 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0072 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0073 | 0/0 | 5389 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0074 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0075 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0076 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0077 | 0/0 | 5389 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0078 | 1/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0079 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0080 | 0/0 | 5407 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0081 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0082 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0083 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0084 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0085 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
t0086 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 0 | 2 | 16 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0002 | 0/0 | 10 | 1 | 2 | 4 | 1 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0006 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0042 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1206 | 155 | 23 | 46 | 57 | 7 | 20 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002 | 0/0 | 1206 | 107 | 12 | 5 | 81 | 1 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003 | 0/0 | 1206 | 84 | 17 | 21 | 26 | 4 | 16 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004 | 0/0 | 1206 | 24 | 12 | 2 | 9 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005 | 0/0 | 1206 | 11 | 11 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0006 | 0/0 | 1206 | 11 | 6 | 1 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0007 | 0/0 | 1206 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0010 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0011 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0012 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0013 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0014 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0002c0008 | 0/0 | 1206 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0003c0009 | 0/0 | 1206 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0004c0016 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0005c0015 | 0/0 | 1206 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6595 | 11 | 1 | 5 | 2 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0002 | 0/0 | 6601 | 12 | 0 | 10 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0003 | 0/0 | 6595 | 55 | 3 | 10 | 33 | 1 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0004 | 0/0 | 6595 | 17 | 0 | 8 | 9 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0006 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0007 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0008 | 0/0 | 6596 | 4 | 2 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0010 | 0/0 | 6595 | 6 | 0 | 3 | 0 | 2 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0011 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0012 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0013 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0017 | 0/0 | 6594 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0020 | 0/0 | 6601 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0022 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0025 | 0/0 | 6594 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0027 | 0/0 | 6595 | 2 | 0 | 0 | 1 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0028 | 0/0 | 6594 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0029 | 0/1 | 6595 | 2 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0030 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0031 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0033 | 0/0 | 6595 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0034 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0041 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0043 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0045 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0046 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0054 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0056 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0057 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0058 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0059 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0060 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0061 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0062 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0064 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0065 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0066 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0069 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0071 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0078 | 1/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0080 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0085 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0001t0086 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0001 | 0/0 | 6595 | 70 | 3 | 5 | 54 | 0 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0003 | 0/0 | 6595 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0004 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0005 | 0/0 | 6594 | 2 | 1 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0007 | 0/0 | 6595 | 4 | 4 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0008 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0009 | 0/0 | 6595 | 8 | 0 | 0 | 7 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0011 | 0/0 | 6595 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0012 | 0/0 | 6596 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0037 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0047 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0048 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0049 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0050 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0051 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0052 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0053 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0063 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0068 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0002t0081 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0002 | 0/0 | 6601 | 57 | 10 | 15 | 19 | 4 | 9 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0003 | 0/0 | 6595 | 6 | 0 | 1 | 2 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0014 | 0/0 | 6601 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0015 | 0/0 | 6601 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0016 | 0/0 | 6601 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0021 | 0/0 | 6602 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0022 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0023 | 0/0 | 6600 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0024 | 0/0 | 6601 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0038 | 0/0 | 6600 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0039 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0040 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0044 | 0/0 | 6601 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0003t0055 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0001 | 0/0 | 6595 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0005 | 0/0 | 6594 | 13 | 8 | 1 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0070 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0072 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0073 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0074 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0075 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0076 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0004t0077 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0007 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0008 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0026 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0035 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0036 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0082 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0083 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0005t0084 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0006t0006 | 0/0 | 6595 | 8 | 4 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0006t0008 | 0/0 | 6596 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0006t0079 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0007t0018 | 0/0 | 6594 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0010t0002 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0010t0042 | 0/0 | 6600 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0011t0002 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0012t0067 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0013t0002 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0001c0014t0002 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0002c0008t0013 | 0/0 | 6595 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0003c0009t0032 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0004c0016t0005 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
a0005c0015t0005 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | copy fasta | chr3 | 33109014 | 33152773 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0001 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0008g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0012g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0017g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0019g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0020g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0020g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0025g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0027g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0027g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0028g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0028g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0029g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0029g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0030g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0030g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0031g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0033g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0034g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0041g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0043g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0045g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0046g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0054g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0056g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0057g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0058g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0059g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0060g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0061g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0062g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0064g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0065g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0066g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0069g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0071g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0078g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0080g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0085g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0086g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0006 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0012g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0012g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0037g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0047g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0048g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0049g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0050g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0051g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0052g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0053g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0063g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0068g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0081g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0002 | 0/0 | 10 | 1 | 2 | 4 | 1 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0022g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0023g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0024g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0038g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0039g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0040g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0044g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0055g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0070g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0072g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0073g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0074g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0075g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0076g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0077g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0026g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0035g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0036g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0082g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0083g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0084g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0079g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0007t0018g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0007t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0007t0018g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0010t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0010t0042g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0011t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0012t0067g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0013t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0014t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0003c0009t0032g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0004c0016t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0005c0015t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0002 | g0140 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00099 | hp2 | a0001 | c0001 | t0085 | g0003 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00140 | hp1 | a0001 | c0001 | t0027 | g0182 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00280 | hp1 | a0001 | c0002 | t0009 | g0222 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0141 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00408 | hp2 | a0001 | c0003 | t0002 | g0113 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00438 | hp1 | a0001 | c0004 | t0072 | g0074 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00544 | hp1 | a0001 | c0001 | t0064 | g0098 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00544 | hp2 | a0001 | c0006 | t0006 | g0054 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00558 | hp1 | a0001 | c0003 | t0021 | g0164 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0234 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00609 | hp1 | a0001 | c0001 | t0058 | g0084 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00639 | hp2 | a0001 | c0007 | t0018 | g0201 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0135 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00673 | hp1 | a0001 | c0002 | t0009 | g0231 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00735 | hp1 | a0001 | c0001 | t0012 | g0100 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0010 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01069 | hp2 | a0001 | c0003 | t0040 | g0130 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0023 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01074 | hp2 | a0001 | c0003 | t0015 | g0271 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0149 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0125 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0023 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01106 | hp1 | a0001 | c0003 | t0039 | g0011 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01106 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01109 | hp1 | a0001 | c0003 | t0055 | g0027 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01109 | hp2 | a0001 | c0004 | t0077 | g0075 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0151 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01168 | hp2 | a0001 | c0013 | t0002 | g0212 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0180 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01243 | hp2 | a0001 | c0004 | t0005 | g0067 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01255 | hp2 | a0001 | c0006 | t0008 | g0178 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01261 | hp2 | a0001 | c0003 | t0014 | g0173 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0010 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01433 | hp1 | a0001 | c0001 | t0033 | g0022 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01433 | hp2 | a0001 | c0001 | t0043 | g0307 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01515 | hp1 | a0003 | c0009 | t0032 | g0045 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0118 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01516 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0003 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01517 | hp1 | a0001 | c0001 | t0010 | g0183 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01517 | hp2 | a0003 | c0009 | t0032 | g0045 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01891 | hp1 | a0001 | c0001 | t0031 | g0019 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01891 | hp2 | a0001 | c0004 | t0005 | g0058 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01934 | hp1 | a0001 | c0001 | t0060 | g0001 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01934 | hp2 | a0001 | c0011 | t0002 | g0252 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0288 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01978 | hp1 | a0001 | c0001 | t0054 | g0004 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0110 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0122 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02015 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02055 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02056 | hp1 | a0001 | c0002 | t0051 | g0015 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02074 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02083 | hp1 | a0001 | c0003 | t0016 | g0127 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02129 | hp1 | a0001 | c0001 | t0028 | g0081 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02135 | hp1 | a0001 | c0002 | t0011 | g0259 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02145 | hp1 | a0001 | c0001 | t0020 | g0046 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02145 | hp2 | a0001 | c0006 | t0006 | g0177 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02148 | hp2 | a0001 | c0001 | t0029 | g0080 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02155 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02165 | hp1 | a0001 | c0003 | t0003 | g0160 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0111 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02257 | hp2 | a0001 | c0010 | t0042 | g0066 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02258 | hp1 | a0001 | c0005 | t0026 | g0280 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0244 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0028 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02280 | hp2 | a0001 | c0004 | t0005 | g0008 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02300 | hp1 | a0001 | c0001 | t0020 | g0308 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02451 | hp1 | a0001 | c0003 | t0022 | g0012 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02451 | hp2 | a0001 | c0005 | t0007 | g0274 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0161 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0263 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02572 | hp1 | a0001 | c0003 | t0015 | g0273 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0172 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02615 | hp1 | a0001 | c0001 | t0065 | g0311 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0166 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02622 | hp2 | a0001 | c0005 | t0026 | g0279 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02630 | hp1 | a0001 | c0001 | t0086 | g0270 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02630 | hp2 | a0001 | c0014 | t0002 | g0281 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02647 | hp1 | a0001 | c0002 | t0008 | g0203 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02647 | hp2 | a0001 | c0004 | t0005 | g0071 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02698 | hp1 | a0001 | c0001 | t0034 | g0038 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02717 | hp1 | a0001 | c0006 | t0006 | g0179 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0301 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02735 | hp1 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02735 | hp2 | a0001 | c0003 | t0003 | g0026 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02738 | hp1 | a0001 | c0003 | t0002 | g0025 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02809 | hp1 | a0001 | c0007 | t0018 | g0202 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02809 | hp2 | a0001 | c0004 | t0005 | g0076 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0210 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02886 | hp2 | a0001 | c0006 | t0079 | g0056 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02895 | hp1 | a0001 | c0005 | t0019 | g0197 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02896 | hp1 | a0001 | c0006 | t0006 | g0175 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02896 | hp2 | a0001 | c0002 | t0037 | g0221 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02897 | hp1 | a0001 | c0006 | t0006 | g0174 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02922 | hp1 | a0001 | c0001 | t0019 | g0159 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0068 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0028 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02970 | hp2 | a0001 | c0003 | t0024 | g0037 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02976 | hp1 | a0001 | c0005 | t0035 | g0313 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03017 | hp1 | a0001 | c0003 | t0002 | g0156 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03017 | hp2 | a0002 | c0008 | t0013 | g0050 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0069 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03098 | hp1 | a0001 | c0004 | t0070 | g0265 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03098 | hp2 | a0001 | c0001 | t0022 | g0167 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0171 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0302 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03139 | hp1 | a0001 | c0005 | t0083 | g0192 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0291 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0243 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03209 | hp1 | a0001 | c0005 | t0008 | g0193 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03209 | hp2 | a0001 | c0004 | t0005 | g0008 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03225 | hp1 | a0001 | c0002 | t0050 | g0242 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03225 | hp2 | a0001 | c0002 | t0052 | g0211 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03453 | hp2 | a0001 | c0006 | t0008 | g0176 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03490 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0133 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03492 | hp1 | a0001 | c0003 | t0003 | g0026 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03516 | hp1 | a0001 | c0001 | t0071 | g0188 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03516 | hp2 | a0001 | c0001 | t0066 | g0051 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03540 | hp2 | a0004 | c0016 | t0005 | g0008 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03579 | hp1 | a0001 | c0001 | t0046 | g0298 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0303 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03654 | hp1 | a0001 | c0001 | t0069 | g0086 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03669 | hp1 | a0001 | c0001 | t0025 | g0029 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0025 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03688 | hp1 | a0001 | c0003 | t0002 | g0137 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03688 | hp2 | a0001 | c0003 | t0016 | g0283 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03704 | hp1 | a0001 | c0001 | t0025 | g0029 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0184 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03927 | hp1 | a0001 | c0001 | t0045 | g0105 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0121 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03942 | hp1 | a0001 | c0001 | t0030 | g0282 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03942 | hp2 | a0001 | c0001 | t0034 | g0038 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04115 | hp2 | a0001 | c0003 | t0044 | g0126 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0304 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04184 | hp2 | a0001 | c0003 | t0014 | g0061 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04199 | hp1 | a0002 | c0008 | t0013 | g0049 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04199 | hp2 | a0001 | c0003 | t0002 | g0128 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04204 | hp2 | a0002 | c0008 | t0013 | g0191 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18522 | hp1 | a0001 | c0004 | t0019 | g0070 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18522 | hp2 | a0001 | c0005 | t0082 | g0194 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | CHB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18906 | hp1 | a0001 | c0003 | t0023 | g0168 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18906 | hp2 | a0001 | c0001 | t0031 | g0019 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18939 | hp1 | a0001 | c0002 | t0011 | g0262 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18943 | hp1 | a0001 | c0003 | t0016 | g0299 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18943 | hp2 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18944 | hp2 | a0001 | c0002 | t0053 | g0226 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18946 | hp1 | a0001 | c0002 | t0009 | g0048 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18946 | hp2 | a0001 | c0002 | t0011 | g0036 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18949 | hp2 | a0001 | c0006 | t0006 | g0055 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18950 | hp1 | a0001 | c0006 | t0006 | g0057 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18960 | hp1 | a0005 | c0015 | t0005 | g0073 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18962 | hp1 | a0001 | c0004 | t0005 | g0009 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18962 | hp2 | a0001 | c0001 | t0062 | g0091 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18965 | hp2 | a0001 | c0004 | t0005 | g0278 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18966 | hp2 | a0001 | c0002 | t0081 | g0227 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18969 | hp2 | a0001 | c0002 | t0012 | g0268 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18970 | hp1 | a0001 | c0004 | t0005 | g0009 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18971 | hp1 | a0001 | c0001 | t0027 | g0162 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18974 | hp2 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0120 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18978 | hp2 | a0001 | c0002 | t0063 | g0239 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18981 | hp1 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18986 | hp1 | a0001 | c0002 | t0012 | g0017 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18988 | hp1 | a0001 | c0001 | t0028 | g0082 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18988 | hp2 | a0001 | c0002 | t0012 | g0017 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18989 | hp1 | a0001 | c0001 | t0059 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18990 | hp2 | a0001 | c0002 | t0005 | g0256 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18991 | hp2 | a0001 | c0001 | t0080 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18997 | hp2 | a0001 | c0002 | t0009 | g0228 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18999 | hp1 | a0001 | c0002 | t0011 | g0036 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0223 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19001 | hp1 | a0001 | c0001 | t0061 | g0099 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19002 | hp1 | a0001 | c0003 | t0002 | g0115 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19002 | hp2 | a0001 | c0004 | t0005 | g0009 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19005 | hp1 | a0001 | c0004 | t0076 | g0062 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19010 | hp1 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19030 | hp1 | a0001 | c0010 | t0002 | g0063 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19030 | hp2 | a0001 | c0004 | t0074 | g0064 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19043 | hp1 | a0001 | c0001 | t0017 | g0042 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19043 | hp2 | a0001 | c0012 | t0067 | g0199 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19054 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19054 | hp2 | a0001 | c0002 | t0009 | g0235 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19055 | hp1 | a0001 | c0002 | t0009 | g0218 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19055 | hp2 | a0001 | c0003 | t0002 | g0142 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19058 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19058 | hp2 | a0001 | c0002 | t0049 | g0200 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19062 | hp1 | a0001 | c0003 | t0002 | g0109 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19063 | hp2 | a0001 | c0003 | t0038 | g0123 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19065 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19067 | hp2 | a0001 | c0002 | t0068 | g0196 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19068 | hp1 | a0001 | c0001 | t0011 | g0078 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19075 | hp1 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19075 | hp2 | a0001 | c0002 | t0009 | g0207 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19076 | hp2 | a0001 | c0002 | t0048 | g0277 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19080 | hp1 | a0001 | c0004 | t0073 | g0072 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19080 | hp2 | a0001 | c0004 | t0001 | g0157 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19082 | hp2 | a0001 | c0001 | t0057 | g0083 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19084 | hp2 | a0001 | c0006 | t0006 | g0053 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19085 | hp1 | a0001 | c0003 | t0021 | g0163 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19085 | hp2 | a0001 | c0002 | t0047 | g0017 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19087 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19088 | hp2 | a0001 | c0001 | t0056 | g0150 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19240 | hp1 | a0001 | c0005 | t0084 | g0275 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19240 | hp2 | a0001 | c0004 | t0005 | g0059 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20129 | hp1 | a0001 | c0003 | t0023 | g0195 | AFR | ASW | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | GIH | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20905 | hp2 | a0001 | c0003 | t0014 | g0116 | SAS | GIH | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01123 | hp1 | a0001 | c0001 | t0041 | g0310 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01123 | hp2 | a0001 | c0003 | t0002 | g0138 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02109 | hp1 | a0001 | c0003 | t0002 | g0002 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0170 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02486 | hp1 | a0001 | c0003 | t0024 | g0037 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02486 | hp2 | a0001 | c0003 | t0015 | g0272 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02559 | hp1 | a0001 | c0005 | t0036 | g0312 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03471 | hp1 | a0001 | c0002 | t0007 | g0245 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03471 | hp2 | a0001 | c0005 | t0007 | g0276 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG06807 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG06807 | hp2 | a0001 | c0004 | t0075 | g0065 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0190 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20300 | hp2 | a0001 | c0007 | t0018 | g0266 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0029 | g0090 | REF | REF | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0078 | g0042 | REF | REF | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114372
|
G | T | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.295G>T | p.Gly99Cys | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/7 | 359/6595 | 295/1206 | 99/401 | chr3 | 33114372 | ||
chr3:33124427
|
T | C | 1 | a0002 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.641T>C | p.Val214Ala | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/7 | 705/6595 | 641/1206 | 214/401 | chr3 | 33124427 | ||
chr3:33132608
|
C | G | 1 | a0005 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.976C>G | p.Gln326Glu | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1040/6595 | 976/1206 | 326/401 | chr3 | 33132608 | ||
chr3:33134242
|
G | A | 1 | a0003 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.1129G>A | p.Glu377Lys | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/7 | 1193/6595 | 1129/1206 | 377/401 | chr3 | 33134242 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114290
|
G | A | 6 | a0001c0002a0001c0005a0001c0007others(3): Show | 124 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(121): Show |
synonymous_variant | LOW | c.213G>A | p.Leu71Leu | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/7 | 277/6595 | 213/1206 | 71/401 | chr3 | 33114290 | ||
chr3:33120406
|
C | T | 7 | a0001c0002a0001c0004a0001c0007others(4): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
synonymous_variant | LOW | c.534C>T | p.Asp178Asp | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/7 | 598/6595 | 534/1206 | 178/401 | chr3 | 33120406 | ||
chr3:33120430
|
A | G | 3 | a0001c0006a0001c0012a0001c0014 | 13 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
synonymous_variant | LOW | c.558A>G | p.Ala186Ala | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/7 | 622/6595 | 558/1206 | 186/401 | chr3 | 33120430 | ||
chr3:33130033
|
C | T | 2 | a0001c0007a0001c0012 | 4 | HG00639.hp2 HG02809.hp1 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.888C>T | p.Thr296Thr | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/7 | 952/6595 | 888/1206 | 296/401 | chr3 | 33130033 | ||
chr3:33132664
|
T | G | 5 | a0001c0003a0001c0010a0001c0011others(2): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.1032T>G | p.Thr344Thr | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1096/6595 | 1032/1206 | 344/401 | chr3 | 33132664 | ||
chr3:33132676
|
G | A | 5 | a0001c0003a0001c0010a0001c0011others(2): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.1044G>A | p.Ser348Ser | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1108/6595 | 1044/1206 | 348/401 | chr3 | 33132676 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33142479
|
C | T | 1 | a0001c0001t0086 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 31 | chr3 | 33142479 | |||||
chr3:33142717
|
C | T | 2 | a0001c0001t0010a0001c0001t0085 | 7 | HG00099.hp2 HG01106.hp2 HG01243.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 269 | chr3 | 33142717 | |||||
chr3:33142736
|
C | T | 4 | a0001c0001t0019a0001c0004t0019a0001c0005t0019others(1): Show | 4 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*288C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 288 | chr3 | 33142736 | |||||
chr3:33143225
|
C | A | 2 | a0001c0005t0035a0001c0005t0036 | 2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 777 | chr3 | 33143225 | |||||
chr3:33143430
|
A | G | 1 | a0001c0002t0009 | 8 | HG00280.hp1 HG00558.hp2 HG00673.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*982A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 982 | chr3 | 33143430 | |||||
chr3:33143489
|
C | T | 2 | a0001c0005t0082a0001c0005t0083 | 2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1041 | chr3 | 33143489 | |||||
chr3:33143502
|
T | C | 1 | a0001c0002t0037 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1054 | chr3 | 33143502 | |||||
chr3:33143535
|
G | GGAACTA | 22 | a0001c0001t0002a0001c0001t0020a0001c0001t0022others(19): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1090_*1095dupACTA others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1096 | INFO_REALIGN_3_PRIME | chr3 | 33143535 | ||||
chr3:33143572
|
C | A | 1 | a0001c0001t0025 | 2 | HG03669.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1124 | chr3 | 33143572 | |||||
chr3:33143623
|
A | C | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1175A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1175 | chr3 | 33143623 | |||||
chr3:33143649
|
A | ATGTAGTG others(10): Show |
1 | a0001c0001t0080 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1204_*1220dupTAGT others(13): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1221 | INFO_REALIGN_3_PRIME | chr3 | 33143649 | ||||
chr3:33143651
|
G | T | 1 | a0001c0002t0081 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1203G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1203 | chr3 | 33143651 | |||||
chr3:33143656
|
G | T | 1 | a0001c0002t0081 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1208G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1208 | chr3 | 33143656 | |||||
chr3:33143809
|
G | A | 1 | a0001c0001t0045 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1361G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1361 | chr3 | 33143809 | |||||
chr3:33143915
|
G | A | 29 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(26): Show | 126 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1467G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1467 | chr3 | 33143915 | |||||
chr3:33144030
|
C | A | 22 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(19): Show | 94 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1582C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1582 | chr3 | 33144030 | |||||
chr3:33144306
|
T | A | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*1858T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1858 | chr3 | 33144306 | |||||
chr3:33144309
|
A | G | 1 | a0001c0003t0044 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1861A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1861 | chr3 | 33144309 | |||||
chr3:33144367
|
A | G | 12 | a0001c0001t0025a0001c0001t0064a0001c0002t0005others(9): Show | 26 | HG00438.hp1 HG00544.hp1 HG01109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1919A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1919 | chr3 | 33144367 | |||||
chr3:33144595
|
A | G | 26 | a0001c0001t0003a0001c0001t0010a0001c0001t0025others(23): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2147A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2147 | chr3 | 33144595 | |||||
chr3:33144864
|
T | C | 36 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(33): Show | 153 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2416T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2416 | chr3 | 33144864 | |||||
chr3:33144922
|
T | G | 2 | a0001c0001t0020a0001c0001t0043 | 3 | HG01433.hp2 HG02145.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2474T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2474 | chr3 | 33144922 | |||||
chr3:33145076
|
G | A | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2628G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2628 | chr3 | 33145076 | |||||
chr3:33145136
|
G | A | 3 | a0001c0001t0019a0001c0004t0019a0001c0005t0019 | 3 | HG02895.hp1 HG02922.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2688G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2688 | chr3 | 33145136 | |||||
chr3:33145324
|
C | T | 2 | a0001c0004t0077a0001c0005t0036 | 2 | HG01109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2876C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2876 | chr3 | 33145324 | |||||
chr3:33145349
|
G | C | 15 | a0001c0001t0025a0001c0001t0028a0001c0001t0031others(12): Show | 31 | HG00438.hp1 HG00609.hp1 HG01243.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2901G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2901 | chr3 | 33145349 | |||||
chr3:33145391
|
A | G | 2 | a0001c0002t0050a0001c0003t0055 | 2 | HG01109.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2943A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2943 | chr3 | 33145391 | |||||
chr3:33145453
|
G | A | 5 | a0001c0001t0007a0001c0001t0046a0001c0002t0007others(2): Show | 10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3005G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3005 | chr3 | 33145453 | |||||
chr3:33145572
|
G | A | 1 | a0001c0004t0072 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3124G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3124 | chr3 | 33145572 | |||||
chr3:33145578
|
A | G | 1 | a0001c0005t0035 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3130A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3130 | chr3 | 33145578 | |||||
chr3:33145590
|
G | A | 19 | a0001c0001t0003a0001c0001t0010a0001c0001t0029others(16): Show | 90 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3142G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3142 | chr3 | 33145590 | |||||
chr3:33145593
|
A | G | 5 | a0001c0001t0007a0001c0001t0046a0001c0002t0007others(2): Show | 10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3145A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3145 | chr3 | 33145593 | |||||
chr3:33145691
|
A | C | 5 | a0001c0001t0007a0001c0001t0046a0001c0002t0007others(2): Show | 10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3243A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3243 | chr3 | 33145691 | |||||
chr3:33145817
|
G | A | 1 | a0001c0001t0059 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3369G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3369 | chr3 | 33145817 | |||||
chr3:33145902
|
C | T | 1 | a0001c0001t0071 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3454C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3454 | chr3 | 33145902 | |||||
chr3:33145912
|
A | C | 1 | a0001c0005t0082 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3464A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3464 | chr3 | 33145912 | |||||
chr3:33145933
|
G | A | 20 | a0001c0001t0002a0001c0001t0020a0001c0001t0022others(17): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3485G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3485 | chr3 | 33145933 | |||||
chr3:33146028
|
T | TA | 5 | a0001c0001t0012a0001c0001t0057a0001c0002t0012others(2): Show | 8 | HG00558.hp1 HG00735.hp1 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3592dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3593 | INFO_REALIGN_3_PRIME | chr3 | 33146028 | ||||
chr3:33146035
|
A | C | 1 | a0001c0001t0085 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3587A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3587 | chr3 | 33146035 | |||||
chr3:33146040
|
AC | A | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3593delC | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3593 | chr3 | 33146040 | |||||
chr3:33146183
|
C | T | 1 | a0001c0012t0067 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3735C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3735 | chr3 | 33146183 | |||||
chr3:33146241
|
C | T | 16 | a0001c0001t0025a0001c0001t0028a0001c0001t0031others(13): Show | 32 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3793C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3793 | chr3 | 33146241 | |||||
chr3:33146320
|
T | C | 1 | a0001c0004t0073 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3872T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3872 | chr3 | 33146320 | |||||
chr3:33146339
|
C | A | 2 | a0001c0001t0022a0001c0003t0022 | 2 | HG02451.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3891C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3891 | chr3 | 33146339 | |||||
chr3:33146339
|
C | T | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(22): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3891C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3891 | chr3 | 33146339 | |||||
chr3:33146361
|
C | T | 1 | a0001c0004t0074 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3913 | chr3 | 33146361 | |||||
chr3:33146397
|
C | T | 16 | a0001c0001t0025a0001c0001t0028a0001c0001t0031others(13): Show | 32 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3949C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3949 | chr3 | 33146397 | |||||
chr3:33146572
|
G | A | 1 | a0001c0003t0039 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4124G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4124 | chr3 | 33146572 | |||||
chr3:33146577
|
T | C | 1 | a0001c0001t0031 | 2 | HG01891.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4129T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4129 | chr3 | 33146577 | |||||
chr3:33146592
|
A | G | 2 | a0001c0001t0062a0001c0001t0064 | 2 | HG00544.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4144A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4144 | chr3 | 33146592 | |||||
chr3:33146638
|
C | T | 1 | a0001c0001t0061 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4190C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4190 | chr3 | 33146638 | |||||
chr3:33146699
|
G | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4251G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4251 | chr3 | 33146699 | |||||
chr3:33146704
|
A | G | 17 | a0001c0001t0025a0001c0001t0028a0001c0001t0031others(14): Show | 33 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4256 | chr3 | 33146704 | |||||
chr3:33146892
|
T | TA | 5 | a0001c0001t0008a0001c0002t0008a0001c0005t0008others(2): Show | 9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4457dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4458 | INFO_REALIGN_3_PRIME | chr3 | 33146892 | ||||
chr3:33146892
|
TA | T | 23 | a0001c0001t0017a0001c0001t0025a0001c0001t0028others(20): Show | 41 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4457delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4457 | INFO_REALIGN_3_PRIME | chr3 | 33146892 | ||||
chr3:33147071
|
A | C | 1 | a0001c0001t0041 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4623A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4623 | chr3 | 33147071 | |||||
chr3:33147153
|
G | T | 1 | a0001c0005t0036 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4705G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4705 | chr3 | 33147153 | |||||
chr3:33147199
|
T | C | 1 | a0001c0003t0040 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4751T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4751 | chr3 | 33147199 | |||||
chr3:33147222
|
C | T | 10 | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(7): Show | 26 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4774C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4774 | chr3 | 33147222 | |||||
chr3:33147453
|
G | T | 1 | a0001c0004t0070 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5005G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5005 | chr3 | 33147453 | |||||
chr3:33147482
|
C | T | 1 | a0001c0010t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5034C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5034 | chr3 | 33147482 | |||||
chr3:33147488
|
A | G | 1 | a0001c0006t0079 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5040A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5040 | chr3 | 33147488 | |||||
chr3:33147718
|
A | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5270A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5270 | chr3 | 33147718 | |||||
chr3:33147719
|
A | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5271 | chr3 | 33147719 | |||||
chr3:33147723
|
A | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5275A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5275 | chr3 | 33147723 | |||||
chr3:33147724
|
A | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5276A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5276 | chr3 | 33147724 | |||||
chr3:33147726
|
G | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5278G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5278 | chr3 | 33147726 | |||||
chr3:33147728
|
T | A | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5280T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5280 | chr3 | 33147728 | |||||
chr3:33147730
|
T | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5282T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5282 | chr3 | 33147730 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114624
|
G | T | 1 | a0001c0001t0003g0316 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471+76G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114624 | ||||||
chr3:33114643
|
C | T | 1 | a0001c0001t0003g0315 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.471+95C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114643 | ||||||
chr3:33114643
|
CTCCAGTT others(8): Show |
C | 1 | a0001c0002t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.471+96_471+110delT others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114643 | ||||||
chr3:33114664
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+116C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114664 | ||||||
chr3:33114675
|
G | T | 2 | a0001c0005t0035g0313a0001c0005t0036g0312 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.471+127G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114675 | ||||||
chr3:33114704
|
T | C | 293 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(290): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.471+156T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114704 | ||||||
chr3:33114718
|
T | C | 1 | a0001c0002t0009g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.471+170T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114718 | ||||||
chr3:33114722
|
C | G | 1 | a0001c0014t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+174C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114722 | ||||||
chr3:33114777
|
C | G | 1 | a0001c0014t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+229C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114777 | ||||||
chr3:33114799
|
C | A | 1 | a0001c0014t0002g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+251C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114799 | ||||||
chr3:33114802
|
C | T | 2 | a0001c0005t0026g0279a0001c0005t0026g0280 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.471+254C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114802 | ||||||
chr3:33114813
|
C | T | 1 | a0001c0004t0005g0278 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+265C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114813 | ||||||
chr3:33114843
|
A | G | 111 | a0001c0001t0086g0270a0001c0002t0001g0006a0001c0002t0001g0007others(108): Show | 132 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.471+295A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114843 | ||||||
chr3:33114866
|
C | T | 1 | a0002c0008t0013g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.471+318C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114866 | ||||||
chr3:33114955
|
T | G | 1 | a0001c0001t0003g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.471+407T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114955 | ||||||
chr3:33114974
|
C | T | 11 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0046others(8): Show | 14 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.471+426C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114974 | ||||||
chr3:33115008
|
A | G | 2 | a0001c0005t0026g0279a0001c0005t0026g0280 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.471+460A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115008 | ||||||
chr3:33115553
|
C | G | 1 | a0001c0002t0048g0277 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.471+1005C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115553 | ||||||
chr3:33115656
|
A | T | 1 | a0001c0001t0003g0305 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+1108A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115656 | ||||||
chr3:33115661
|
T | A | 2 | a0002c0008t0013g0049a0002c0008t0013g0050 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.471+1113T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115661 | ||||||
chr3:33115758
|
T | G | 1 | a0001c0001t0003g0316 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471+1210T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115758 | ||||||
chr3:33115779
|
A | G | 3 | a0001c0005t0007g0274a0001c0005t0007g0276a0001c0005t0084g0275 | 3 | HG02451.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.471+1231A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115779 | ||||||
chr3:33115877
|
C | T | 5 | a0001c0001t0086g0270a0001c0003t0015g0271a0001c0003t0015g0272others(2): Show | 6 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+1329C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115877 | ||||||
chr3:33115923
|
T | TA | 16 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(13): Show | 18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1384dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33115923 | |||||
chr3:33115968
|
A | C | 16 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(13): Show | 18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1420A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115968 | ||||||
chr3:33116024
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0306 | 3 | HG00140.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.471+1476T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116024 | ||||||
chr3:33116179
|
A | T | 4 | a0001c0002t0001g0269a0001c0002t0012g0017a0001c0002t0012g0268others(1): Show | 5 | NA18969.hp2 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+1631A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116179 | ||||||
chr3:33116360
|
A | G | 21 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0003g0003others(18): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.471+1812A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116360 | ||||||
chr3:33116384
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.471+1836A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116384 | ||||||
chr3:33116451
|
A | G | 16 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(13): Show | 18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1903A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116451 | ||||||
chr3:33116655
|
A | G | 16 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(13): Show | 18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+2107A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116655 | ||||||
chr3:33116661
|
G | A | 1 | a0001c0002t0001g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+2113G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116661 | ||||||
chr3:33116727
|
C | T | 1 | a0001c0007t0018g0266 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471+2179C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116727 | ||||||
chr3:33116791
|
T | C | 17 | a0001c0001t0003g0052a0001c0001t0031g0019a0001c0001t0066g0051others(14): Show | 19 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+2243T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116791 | ||||||
chr3:33116827
|
T | C | 22 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(19): Show | 24 | HG00544.hp2 HG01074.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.471+2279T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116827 | ||||||
chr3:33116831
|
C | T | 1 | a0001c0003t0014g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.471+2283C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116831 | ||||||
chr3:33117107
|
C | CA | 17 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0001t0086g0270others(14): Show | 19 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+2567dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117107 | |||||
chr3:33117127
|
G | A | 23 | a0001c0001t0002g0060a0001c0003t0014g0061a0001c0004t0005g0008others(20): Show | 26 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.471+2579G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117127 | ||||||
chr3:33117177
|
A | G | 1 | a0001c0004t0070g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.471+2629A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117177 | ||||||
chr3:33117178
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.471+2630T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117178 | ||||||
chr3:33117256
|
T | C | 6 | a0001c0006t0006g0174a0001c0006t0006g0175a0001c0006t0006g0177others(3): Show | 6 | HG01255.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+2708T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117256 | ||||||
chr3:33117420
|
G | A | 282 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(279): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.471+2872G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117420 | ||||||
chr3:33117425
|
A | G | 1 | a0001c0002t0001g0264 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.471+2877A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117425 | ||||||
chr3:33117459
|
C | A | 3 | a0001c0001t0086g0270a0001c0003t0015g0271a0001c0003t0015g0272 | 3 | HG01074.hp2 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.472-2885C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117459 | ||||||
chr3:33117711
|
C | T | 12 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0255others(9): Show | 13 | HG02027.hp1 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.472-2633C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117711 | ||||||
chr3:33117774
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(114): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.472-2570A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117774 | ||||||
chr3:33117861
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.472-2483C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117861 | ||||||
chr3:33117948
|
A | ATTCC | 2 | a0001c0001t0031g0019a0001c0001t0066g0051 | 3 | HG01891.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.472-2393_472-2390d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117948 | |||||
chr3:33117951
|
C | CCTTT | 9 | a0001c0001t0011g0078a0001c0002t0068g0196a0001c0004t0005g0058others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-2372_472-2369d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117951 | |||||
chr3:33118255
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.472-2089G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118255 | ||||||
chr3:33118304
|
A | G | 6 | a0001c0001t0001g0165a0001c0001t0027g0162a0001c0003t0003g0160others(3): Show | 6 | HG00408.hp1 HG00558.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-2040A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118304 | ||||||
chr3:33118311
|
C | T | 3 | a0001c0001t0031g0019a0001c0001t0066g0051a0001c0004t0070g0265 | 4 | HG01891.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-2033C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118311 | ||||||
chr3:33118320
|
G | A | 1 | a0001c0002t0012g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-2024G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118320 | ||||||
chr3:33118455
|
A | C | 3 | a0001c0001t0019g0159a0001c0005t0026g0279a0001c0005t0026g0280 | 3 | HG02258.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.472-1889A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118455 | ||||||
chr3:33118574
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.472-1770A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118574 | ||||||
chr3:33118884
|
G | A | 5 | a0001c0001t0086g0270a0001c0003t0015g0271a0001c0003t0015g0272others(2): Show | 6 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-1460G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118884 | ||||||
chr3:33118915
|
G | A | 231 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.472-1429G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118915 | ||||||
chr3:33118943
|
G | A | 1 | a0001c0005t0007g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.472-1401G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118943 | ||||||
chr3:33118944
|
G | A | 1 | a0001c0005t0007g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.472-1400G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118944 | ||||||
chr3:33119062
|
T | C | 2 | a0001c0002t0001g0198a0001c0002t0001g0267 | 2 | HG00621.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.472-1282T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119062 | ||||||
chr3:33119213
|
A | G | 1 | a0001c0001t0003g0154 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472-1131A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119213 | ||||||
chr3:33119246
|
A | G | 2 | a0002c0008t0013g0049a0002c0008t0013g0050 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.472-1098A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119246 | ||||||
chr3:33119251
|
T | C | 6 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(3): Show | 6 | HG00544.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-1093T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119251 | ||||||
chr3:33119311
|
A | C | 1 | a0001c0001t0065g0311 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.472-1033A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119311 | ||||||
chr3:33119403
|
A | G | 8 | a0001c0002t0001g0007a0001c0002t0001g0246a0001c0002t0001g0247others(5): Show | 11 | HG00609.hp2 HG02027.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-941A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119403 | ||||||
chr3:33119498
|
A | AT | 19 | a0001c0001t0007g0190a0001c0003t0015g0271a0001c0003t0015g0272others(16): Show | 20 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.472-837dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119498 | |||||
chr3:33119498
|
A | ATTT | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-839_472-837dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119498 | |||||
chr3:33119520
|
ATTG | A | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-821_472-819del others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119520 | |||||
chr3:33119606
|
T | C | 1 | a0001c0004t0076g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.472-738T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119606 | ||||||
chr3:33119614
|
T | C | 1 | a0001c0002t0001g0253 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.472-730T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119614 | ||||||
chr3:33119621
|
T | C | 2 | a0001c0003t0023g0195a0001c0011t0002g0252 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.472-723T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119621 | ||||||
chr3:33119661
|
A | C | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-683A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119661 | ||||||
chr3:33119673
|
G | T | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-671G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119673 | ||||||
chr3:33119766
|
A | G | 6 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(3): Show | 6 | HG00544.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-578A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119766 | ||||||
chr3:33119777
|
A | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0153 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.472-567A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119777 | ||||||
chr3:33119862
|
C | T | 1 | a0001c0003t0002g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.472-482C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119862 | ||||||
chr3:33119863
|
G | A | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-481G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119863 | ||||||
chr3:33119882
|
T | C | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.472-462T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119882 | ||||||
chr3:33119912
|
T | C | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-432T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119912 | ||||||
chr3:33119942
|
G | A | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-402G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119942 | ||||||
chr3:33120087
|
G | A | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-257G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120087 | ||||||
chr3:33120208
|
C | A | 7 | a0001c0005t0007g0276a0001c0005t0008g0193a0001c0005t0035g0313others(4): Show | 7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-136C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120208 | ||||||
chr3:33120210
|
T | G | 1 | a0001c0002t0049g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.472-134T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120210 | ||||||
chr3:33120237
|
A | G | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-107A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120237 | ||||||
chr3:33120253
|
A | G | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-91A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120253 | ||||||
chr3:33120591
|
T | C | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.621+98T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120591 | ||||||
chr3:33120679
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0027g0162a0001c0003t0021g0163others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+186C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120679 | ||||||
chr3:33120681
|
G | A | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.621+188G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120681 | ||||||
chr3:33120757
|
A | C | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+264A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120757 | ||||||
chr3:33120821
|
A | G | 2 | a0001c0003t0023g0195a0001c0011t0002g0252 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.621+328A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120821 | ||||||
chr3:33120871
|
T | A | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+378T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120871 | ||||||
chr3:33120884
|
C | T | 1 | a0001c0001t0056g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.621+391C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120884 | ||||||
chr3:33120972
|
A | T | 2 | a0002c0008t0013g0049a0002c0008t0013g0050 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.621+479A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120972 | ||||||
chr3:33120998
|
G | A | 10 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0003g0003others(7): Show | 12 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+505G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120998 | ||||||
chr3:33121040
|
A | C | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+547A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121040 | ||||||
chr3:33121130
|
T | C | 116 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(113): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+637T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121130 | ||||||
chr3:33121175
|
G | A | 1 | a0001c0004t0070g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+682G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121175 | ||||||
chr3:33121254
|
C | T | 1 | a0001c0003t0002g0149 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.621+761C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121254 | ||||||
chr3:33121256
|
A | G | 90 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0013others(87): Show | 110 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.621+763A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121256 | ||||||
chr3:33121270
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(140): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.621+777G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121270 | ||||||
chr3:33121344
|
A | G | 26 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(23): Show | 29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+851A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121344 | ||||||
chr3:33121354
|
A | G | 26 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(23): Show | 29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+861A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121354 | ||||||
chr3:33121369
|
G | A | 1 | a0001c0001t0028g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.621+876G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121369 | ||||||
chr3:33121380
|
C | T | 26 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(23): Show | 29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+887C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121380 | ||||||
chr3:33121385
|
C | G | 1 | a0001c0004t0005g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+892C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121385 | ||||||
chr3:33121410
|
T | C | 4 | a0001c0001t0028g0081a0001c0001t0028g0082a0001c0001t0057g0083others(1): Show | 4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+917T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121410 | ||||||
chr3:33121411
|
C | CAAAAAAA others(8): Show |
20 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(17): Show | 23 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.621+926_621+927ins others(15): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | |||||
chr3:33121411
|
C | CAAAAAAA others(9): Show |
3 | a0001c0004t0070g0265a0001c0004t0074g0064a0001c0010t0002g0063 | 3 | HG03098.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.621+926_621+927ins others(16): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | |||||
chr3:33121411
|
C | CAAAAAAA others(10): Show |
3 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.621+926_621+927ins others(17): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | |||||
chr3:33121487
|
G | A | 7 | a0001c0005t0007g0276a0001c0005t0008g0193a0001c0005t0035g0313others(4): Show | 7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+994G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121487 | ||||||
chr3:33121495
|
TAG | T | 26 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(23): Show | 29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+1005_621+1006d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121495 | |||||
chr3:33121529
|
G | A | 26 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(23): Show | 29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+1036G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121529 | ||||||
chr3:33121602
|
C | T | 1 | a0001c0001t0003g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.621+1109C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121602 | ||||||
chr3:33121761
|
T | C | 1 | a0001c0002t0001g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.621+1268T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121761 | ||||||
chr3:33121791
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.621+1298A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121791 | ||||||
chr3:33121861
|
G | A | 4 | a0001c0001t0019g0159a0001c0005t0019g0197a0001c0005t0026g0279others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1368G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121861 | ||||||
chr3:33121865
|
C | T | 1 | a0001c0004t0070g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+1372C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121865 | ||||||
chr3:33121956
|
G | A | 3 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.621+1463G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121956 | ||||||
chr3:33122019
|
C | T | 1 | a0001c0004t0005g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+1526C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122019 | ||||||
chr3:33122289
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+1796C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122289 | ||||||
chr3:33122290
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+1797C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122290 | ||||||
chr3:33122292
|
C | T | 5 | a0001c0002t0007g0243a0001c0002t0007g0244a0001c0002t0007g0245others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1799C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122292 | ||||||
chr3:33122310
|
A | G | 1 | a0001c0005t0082g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.621+1817A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122310 | ||||||
chr3:33122328
|
A | G | 2 | a0001c0005t0026g0279a0001c0005t0026g0280 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.621+1835A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122328 | ||||||
chr3:33122399
|
G | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(169): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.621+1906G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122399 | ||||||
chr3:33122429
|
G | A | 1 | a0001c0001t0028g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.621+1936G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122429 | ||||||
chr3:33122437
|
C | T | 17 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(14): Show | 18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.621+1944C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122437 | ||||||
chr3:33122490
|
C | T | 1 | a0001c0005t0026g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622-1918C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122490 | ||||||
chr3:33122545
|
A | G | 1 | a0001c0002t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-1863A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122545 | ||||||
chr3:33122587
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.622-1821T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122587 | ||||||
chr3:33122600
|
T | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(113): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.622-1808T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122600 | ||||||
chr3:33122679
|
G | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(278): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.622-1729G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122679 | ||||||
chr3:33122709
|
C | CA | 80 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0043g0307others(77): Show | 100 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.622-1676dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
C | CAA | 9 | a0001c0002t0001g0205a0001c0002t0001g0208a0001c0002t0001g0209others(6): Show | 9 | HG02738.hp2 HG04184.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-1677_622-1676d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
C | CAAAA | 13 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(10): Show | 13 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.622-1679_622-1676d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
CAA | C | 8 | a0001c0001t0019g0159a0001c0004t0074g0064a0001c0004t0075g0065others(5): Show | 8 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-1677_622-1676d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
CAAA | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(150): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.622-1678_622-1676d others(5): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
CAAAA | C | 7 | a0001c0003t0002g0139a0001c0003t0002g0140a0001c0003t0002g0141others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-1679_622-1676d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122709
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-1687_622-1676d others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | |||||
chr3:33122730
|
A | G | 9 | a0001c0001t0001g0185a0001c0001t0002g0181a0001c0001t0003g0003others(6): Show | 11 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-1678A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122730 | ||||||
chr3:33122898
|
G | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(164): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.622-1510G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122898 | ||||||
chr3:33122995
|
G | C | 1 | a0001c0001t0013g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.622-1413G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122995 | ||||||
chr3:33123046
|
C | T | 1 | a0001c0004t0075g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-1362C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123046 | ||||||
chr3:33123137
|
TG | T | 6 | a0001c0002t0007g0210a0001c0002t0007g0243a0001c0002t0007g0244others(3): Show | 6 | HG02258.hp2 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1270delG | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123137 | ||||||
chr3:33123159
|
G | A | 5 | a0001c0002t0001g0013a0001c0002t0001g0205a0001c0002t0001g0213others(2): Show | 7 | HG01168.hp2 HG02055.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-1249G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123159 | ||||||
chr3:33123219
|
G | T | 1 | a0001c0004t0005g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.622-1189G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123219 | ||||||
chr3:33123244
|
C | T | 23 | a0001c0002t0008g0203a0001c0004t0005g0008a0001c0004t0005g0009others(20): Show | 26 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.622-1164C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123244 | ||||||
chr3:33123335
|
T | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(166): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.622-1073T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123335 | ||||||
chr3:33123366
|
G | A | 1 | a0001c0003t0002g0109 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.622-1042G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123366 | ||||||
chr3:33123457
|
C | CTCTT | 169 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(166): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.622-950_622-947dup others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123457 | |||||
chr3:33123488
|
C | T | 276 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(273): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.622-920C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123488 | ||||||
chr3:33123625
|
G | GT | 52 | a0001c0001t0002g0046a0001c0001t0002g0309a0001c0001t0003g0040others(49): Show | 58 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.622-759dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
G | GTT | 10 | a0001c0002t0001g0035a0001c0006t0006g0053a0001c0006t0006g0054others(7): Show | 11 | HG00544.hp2 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-760_622-759dup others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
G | GTTT | 6 | a0001c0001t0007g0190a0001c0003t0015g0272a0001c0003t0015g0273others(3): Show | 7 | HG01255.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-761_622-759dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
GTTTT | G | 16 | a0001c0001t0001g0185a0001c0001t0003g0022a0001c0001t0003g0077others(13): Show | 16 | HG00438.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-762_622-759del others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
GTTTTT | G | 92 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(89): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.622-763_622-759del others(5): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
GTTTTTT | G | 52 | a0001c0001t0001g0117a0001c0001t0001g0165a0001c0001t0003g0114others(49): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.622-764_622-759del others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123625
|
GTTTTTTT | G | 7 | a0001c0001t0001g0024a0001c0001t0065g0311a0001c0003t0002g0023others(4): Show | 9 | HG01074.hp1 HG01099.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-765_622-759del others(7): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | |||||
chr3:33123660
|
C | T | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-748C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123660 | ||||||
chr3:33123716
|
G | A | 1 | a0001c0001t0034g0038 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.622-692G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123716 | ||||||
chr3:33123759
|
A | C | 1 | a0001c0002t0001g0232 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.622-649A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123759 | ||||||
chr3:33123811
|
C | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(166): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.622-597C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123811 | ||||||
chr3:33123830
|
T | C | 3 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.622-578T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123830 | ||||||
chr3:33123926
|
C | A | 1 | a0001c0005t0083g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.622-482C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123926 | ||||||
chr3:33123944
|
T | A | 281 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(278): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.622-464T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123944 | ||||||
chr3:33124019
|
C | G | 1 | a0001c0003t0040g0130 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.622-389C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124019 | ||||||
chr3:33124040
|
A | G | 3 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.622-368A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124040 | ||||||
chr3:33124128
|
T | C | 2 | a0001c0001t0007g0190a0001c0005t0007g0274 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-280T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124128 | ||||||
chr3:33124327
|
G | A | 2 | a0001c0010t0002g0063a0001c0010t0042g0066 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.622-81G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124327 | ||||||
chr3:33124757
|
G | A | 1 | a0001c0003t0002g0112 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.793+178G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124757 | ||||||
chr3:33124864
|
T | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(68): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.793+285T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124864 | ||||||
chr3:33124935
|
A | G | 1 | a0001c0003t0021g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.793+356A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124935 | ||||||
chr3:33124940
|
T | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(278): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.793+361T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124940 | ||||||
chr3:33125491
|
G | GT | 87 | a0001c0001t0001g0004a0001c0001t0001g0155a0001c0001t0002g0046others(84): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.793+936dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | |||||
chr3:33125491
|
G | GTT | 131 | a0001c0001t0001g0024a0001c0001t0001g0101a0001c0001t0001g0117others(128): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.793+935_793+936dup others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | |||||
chr3:33125491
|
G | GTTT | 36 | a0001c0001t0065g0311a0001c0002t0001g0033a0001c0002t0001g0034others(33): Show | 41 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.793+934_793+936dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | |||||
chr3:33125491
|
GT | G | 8 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(5): Show | 9 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+936delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | |||||
chr3:33125683
|
C | T | 3 | a0001c0002t0009g0228a0001c0002t0009g0231a0001c0002t0009g0235 | 3 | HG00673.hp1 NA18997.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.793+1104C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125683 | ||||||
chr3:33125764
|
A | G | 58 | a0001c0001t0001g0024a0001c0001t0001g0117a0001c0001t0003g0114others(55): Show | 75 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.793+1185A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125764 | ||||||
chr3:33125973
|
G | A | 1 | a0001c0001t0004g0286 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.793+1394G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125973 | ||||||
chr3:33126008
|
A | C | 23 | a0001c0002t0008g0203a0001c0003t0002g0125a0001c0004t0005g0008others(20): Show | 26 | HG00438.hp1 HG01081.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.793+1429A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126008 | ||||||
chr3:33126008
|
A | G | 1 | a0001c0003t0002g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.793+1429A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126008 | ||||||
chr3:33126111
|
C | T | 2 | a0001c0005t0007g0276a0001c0005t0084g0275 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.793+1532C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126111 | ||||||
chr3:33126137
|
C | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(128): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.793+1558C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126137 | ||||||
chr3:33126155
|
C | G | 2 | a0001c0003t0015g0271a0001c0003t0015g0272 | 2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.793+1576C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126155 | ||||||
chr3:33126217
|
C | G | 1 | a0001c0002t0081g0227 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.793+1638C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126217 | ||||||
chr3:33126309
|
G | A | 91 | a0001c0001t0001g0165a0001c0002t0001g0006a0001c0002t0001g0007others(88): Show | 111 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.793+1730G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126309 | ||||||
chr3:33126330
|
G | A | 10 | a0001c0005t0007g0276a0001c0005t0008g0193a0001c0005t0035g0313others(7): Show | 10 | HG00639.hp2 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+1751G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126330 | ||||||
chr3:33126361
|
T | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(278): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.793+1782T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126361 | ||||||
chr3:33126379
|
T | C | 1 | a0001c0001t0071g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.793+1800T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126379 | ||||||
chr3:33126410
|
T | G | 7 | a0001c0005t0007g0276a0001c0005t0008g0193a0001c0005t0035g0313others(4): Show | 7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+1831T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126410 | ||||||
chr3:33126456
|
A | G | 2 | a0001c0003t0003g0026a0001c0003t0003g0133 | 3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.793+1877A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126456 | ||||||
chr3:33126509
|
A | C | 1 | a0001c0006t0006g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+1930A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126509 | ||||||
chr3:33126615
|
A | G | 1 | a0005c0015t0005g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+2036A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126615 | ||||||
chr3:33126631
|
A | G | 1 | a0001c0003t0002g0124 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.793+2052A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126631 | ||||||
chr3:33126651
|
C | T | 1 | a0001c0002t0012g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.793+2072C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126651 | ||||||
chr3:33126988
|
G | A | 1 | a0001c0002t0011g0259 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.793+2409G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126988 | ||||||
chr3:33127099
|
CT | C | 251 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(248): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.793+2537delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127099 | |||||
chr3:33127099
|
CTT | C | 9 | a0001c0001t0003g0104a0001c0001t0061g0099a0001c0002t0001g0233others(6): Show | 10 | HG01070.hp1 HG01074.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2536_793+2537d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127099 | |||||
chr3:33127116
|
T | A | 1 | a0001c0003t0024g0037 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.793+2537T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127116 | ||||||
chr3:33127116
|
TA | T | 4 | a0001c0002t0001g0255a0002c0008t0013g0049a0002c0008t0013g0050others(1): Show | 4 | HG03017.hp2 HG04199.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+2540delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127116 | |||||
chr3:33127335
|
C | G | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-2604C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127335 | ||||||
chr3:33127351
|
A | G | 17 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(14): Show | 18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2588A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127351 | ||||||
chr3:33127377
|
G | T | 17 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(14): Show | 18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2562G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127377 | ||||||
chr3:33127435
|
A | G | 3 | a0002c0008t0013g0049a0002c0008t0013g0050a0002c0008t0013g0191 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-2504A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127435 | ||||||
chr3:33127439
|
TTTTATTT others(5): Show |
T | 89 | a0001c0001t0001g0165a0001c0002t0001g0006a0001c0002t0001g0007others(86): Show | 109 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.794-2488_794-2477d others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127439 | |||||
chr3:33127509
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794-2430G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127509 | ||||||
chr3:33127640
|
G | C | 3 | a0002c0008t0013g0049a0002c0008t0013g0050a0002c0008t0013g0191 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-2299G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127640 | ||||||
chr3:33127681
|
C | A | 1 | a0001c0002t0001g0225 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.794-2258C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127681 | ||||||
chr3:33128007
|
C | G | 8 | a0001c0004t0005g0008a0001c0004t0005g0058a0001c0004t0005g0059others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-1932C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128007 | ||||||
chr3:33128345
|
C | A | 2 | a0001c0003t0003g0026a0001c0003t0003g0133 | 3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.794-1594C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128345 | ||||||
chr3:33128543
|
T | A | 1 | a0001c0002t0048g0277 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.794-1396T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128543 | ||||||
chr3:33128761
|
C | T | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-1178C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128761 | ||||||
chr3:33128780
|
A | C | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-1159A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128780 | ||||||
chr3:33128913
|
A | G | 1 | a0001c0002t0001g0258 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.794-1026A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128913 | ||||||
chr3:33129005
|
T | C | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-934T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129005 | ||||||
chr3:33129040
|
T | C | 4 | a0001c0002t0001g0229a0001c0002t0001g0233a0001c0002t0001g0240others(1): Show | 4 | NA18959.hp2 NA18974.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-899T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129040 | ||||||
chr3:33129041
|
G | A | 1 | a0001c0003t0002g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.794-898G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129041 | ||||||
chr3:33129048
|
A | G | 1 | a0001c0002t0052g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.794-891A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129048 | ||||||
chr3:33129385
|
C | T | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-554C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129385 | ||||||
chr3:33129447
|
A | G | 1 | a0001c0012t0067g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.794-492A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129447 | ||||||
chr3:33129459
|
T | G | 3 | a0001c0003t0002g0138a0001c0003t0002g0140a0001c0003t0002g0151 | 3 | HG00099.hp1 HG01123.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.794-480T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129459 | ||||||
chr3:33129529
|
C | A | 1 | a0001c0001t0029g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.794-410C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129529 | ||||||
chr3:33129535
|
C | CT | 65 | a0001c0001t0001g0024a0001c0001t0001g0117a0001c0001t0003g0103others(62): Show | 82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.794-385dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33129535 | |||||
chr3:33129535
|
CT | C | 6 | a0001c0001t0002g0043a0001c0001t0062g0091a0001c0002t0001g0232others(3): Show | 7 | HG00140.hp2 HG01168.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-385delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33129535 | |||||
chr3:33129539
|
T | C | 4 | a0001c0001t0028g0081a0001c0001t0028g0082a0001c0001t0057g0083others(1): Show | 4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-400T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129539 | ||||||
chr3:33129540
|
T | C | 1 | a0001c0001t0019g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794-399T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129540 | ||||||
chr3:33129541
|
T | C | 1 | a0001c0002t0001g0217 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.794-398T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129541 | ||||||
chr3:33129606
|
C | T | 1 | a0001c0001t0043g0307 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.794-333C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129606 | ||||||
chr3:33129639
|
G | A | 2 | a0001c0002t0001g0229a0001c0002t0001g0240 | 2 | NA18974.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.794-300G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129639 | ||||||
chr3:33129648
|
C | T | 13 | a0001c0002t0001g0264a0001c0006t0006g0053a0001c0006t0006g0054others(10): Show | 13 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-291C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129648 | ||||||
chr3:33129676
|
C | T | 6 | a0001c0003t0002g0129a0001c0003t0002g0136a0001c0003t0002g0142others(3): Show | 6 | NA18943.hp1 NA19010.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-263C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129676 | ||||||
chr3:33129687
|
A | G | 2 | a0001c0001t0066g0051a0001c0004t0073g0072 | 2 | HG03516.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.794-252A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129687 | ||||||
chr3:33129691
|
C | T | 2 | a0001c0002t0009g0207a0001c0002t0009g0234 | 2 | HG00558.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.794-248C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129691 | ||||||
chr3:33129699
|
A | G | 2 | a0001c0005t0082g0194a0001c0005t0083g0192 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-240A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129699 | ||||||
chr3:33129744
|
A | G | 3 | a0001c0001t0004g0292a0001c0002t0001g0031a0001c0002t0003g0031 | 3 | HG01496.hp2 NA18612.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.794-195A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129744 | ||||||
chr3:33129758
|
G | A | 2 | a0001c0003t0002g0025a0001c0003t0044g0126 | 3 | HG02738.hp1 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.794-181G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129758 | ||||||
chr3:33129784
|
G | A | 1 | a0001c0004t0073g0072 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.794-155G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129784 | ||||||
chr3:33129826
|
C | A | 1 | a0001c0002t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.794-113C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129826 | ||||||
chr3:33129828
|
C | T | 1 | a0001c0002t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.794-111C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129828 | ||||||
chr3:33129936
|
C | T | 1 | a0001c0004t0019g0070 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.794-3C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129936 | ||||||
chr3:33130167
|
A | G | 296 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(293): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.922+100A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130167 | ||||||
chr3:33130220
|
T | C | 2 | a0001c0002t0001g0246a0001c0002t0001g0250 | 2 | NA18984.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.922+153T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130220 | ||||||
chr3:33130525
|
CT | C | 140 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0020others(137): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.922+483delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | |||||
chr3:33130525
|
CTT | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(118): Show | 147 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.922+482_922+483del others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | |||||
chr3:33130525
|
CTTT | C | 10 | a0001c0001t0001g0165a0001c0001t0007g0291a0001c0001t0046g0298others(7): Show | 11 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.922+481_922+483del others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | |||||
chr3:33130527
|
T | C | 1 | a0001c0002t0001g0217 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.922+460T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130527 | ||||||
chr3:33130531
|
T | C | 3 | a0001c0005t0019g0197a0001c0005t0026g0279a0001c0005t0026g0280 | 3 | HG02258.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.922+464T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130531 | ||||||
chr3:33130532
|
T | C | 5 | a0001c0001t0019g0159a0001c0003t0002g0134a0002c0008t0013g0049others(2): Show | 5 | HG01261.hp1 HG02922.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+465T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130532 | ||||||
chr3:33130734
|
A | G | 1 | a0001c0002t0037g0221 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.922+667A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130734 | ||||||
chr3:33130967
|
C | T | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+900C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130967 | ||||||
chr3:33130968
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.922+901G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130968 | ||||||
chr3:33130971
|
T | C | 5 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(2): Show | 5 | HG00544.hp2 HG02886.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+904T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130971 | ||||||
chr3:33131117
|
C | T | 1 | a0001c0001t0029g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.922+1050C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131117 | ||||||
chr3:33131148
|
C | T | 11 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(8): Show | 11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.922+1081C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131148 | ||||||
chr3:33131200
|
G | A | 1 | a0002c0008t0013g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.922+1133G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131200 | ||||||
chr3:33131211
|
G | A | 2 | a0001c0005t0035g0313a0001c0005t0036g0312 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.922+1144G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131211 | ||||||
chr3:33131253
|
G | GT | 22 | a0001c0001t0013g0166a0001c0001t0031g0019a0001c0001t0086g0270others(19): Show | 23 | HG00544.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.922+1196dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33131253 | |||||
chr3:33131284
|
A | G | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+1217A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131284 | ||||||
chr3:33131308
|
A | T | 22 | a0001c0001t0025g0029a0001c0002t0005g0216a0001c0002t0068g0196others(19): Show | 26 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.922+1241A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131308 | ||||||
chr3:33131525
|
A | G | 2 | a0001c0002t0001g0258a0001c0002t0001g0261 | 2 | NA18947.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.923-1030A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131525 | ||||||
chr3:33131667
|
G | A | 1 | a0001c0012t0067g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.923-888G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131667 | ||||||
chr3:33131695
|
ATGCTAC | A | 4 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-859_923-854del others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131695 | ||||||
chr3:33131702
|
A | C | 4 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-853A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131702 | ||||||
chr3:33131703
|
T | C | 4 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-852T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131703 | ||||||
chr3:33132126
|
G | A | 6 | a0001c0004t0005g0009a0001c0004t0005g0278a0001c0004t0072g0074others(3): Show | 8 | HG00438.hp1 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.923-429G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132126 | ||||||
chr3:33132370
|
G | A | 1 | a0001c0001t0045g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.923-185G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132370 | ||||||
chr3:33132384
|
G | A | 1 | a0001c0005t0084g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923-171G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132384 | ||||||
chr3:33132436
|
C | A | 1 | a0001c0001t0006g0301 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.923-119C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132436 | ||||||
chr3:33132804
|
G | A | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1068+104G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33132804 | ||||||
chr3:33132861
|
T | C | 4 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+161T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33132861 | ||||||
chr3:33133003
|
A | G | 291 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(288): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1068+303A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133003 | ||||||
chr3:33133005
|
G | GA | 291 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(288): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1068+305_1068+306i others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133005 | ||||||
chr3:33133261
|
CT | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(214): Show | 260 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1068+576delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133261 | |||||
chr3:33133382
|
C | G | 1 | a0001c0012t0067g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+682C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133382 | ||||||
chr3:33133384
|
G | A | 10 | a0001c0001t0004g0039a0001c0001t0004g0041a0001c0001t0004g0148others(7): Show | 12 | HG00735.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1068+684G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133384 | ||||||
chr3:33133466
|
T | G | 5 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(2): Show | 5 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-716T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133466 | ||||||
chr3:33133521
|
AT | A | 291 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(288): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1069-658delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133521 | |||||
chr3:33133567
|
C | A | 1 | a0001c0005t0084g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1069-615C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133567 | ||||||
chr3:33133667
|
A | ACTTT | 269 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(266): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1069-514_1069-511d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133667 | |||||
chr3:33133691
|
G | C | 1 | a0001c0004t0005g0278 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1069-491G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133691 | ||||||
chr3:33133936
|
C | A | 9 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0046others(6): Show | 11 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-246C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133936 | ||||||
chr3:33133980
|
A | G | 1 | a0001c0005t0084g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1069-202A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133980 | ||||||
chr3:33134023
|
G | A | 3 | a0002c0008t0013g0049a0002c0008t0013g0050a0002c0008t0013g0191 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1069-159G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33134023 | ||||||
chr3:33134058
|
A | G | 1 | a0001c0002t0053g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1069-124A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33134058 | ||||||
chr3:33134301
|
C | A | 296 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(293): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1152+36C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134301 | ||||||
chr3:33134362
|
A | G | 71 | a0001c0003t0002g0002a0001c0003t0002g0010a0001c0003t0002g0011others(68): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1152+97A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134362 | ||||||
chr3:33134440
|
G | A | 2 | a0001c0001t0007g0190a0001c0005t0007g0276 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1152+175G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134440 | ||||||
chr3:33134453
|
A | G | 2 | a0001c0002t0001g0253a0001c0002t0001g0257 | 2 | HG02027.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1152+188A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134453 | ||||||
chr3:33134673
|
G | A | 1 | a0001c0001t0028g0082 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1152+408G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134673 | ||||||
chr3:33134743
|
C | T | 5 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(2): Show | 5 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152+478C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134743 | ||||||
chr3:33134761
|
T | A | 1 | a0001c0001t0004g0286 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1152+496T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134761 | ||||||
chr3:33134803
|
G | A | 3 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1152+538G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134803 | ||||||
chr3:33134884
|
G | A | 2 | a0001c0003t0015g0271a0001c0003t0015g0272 | 2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1152+619G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134884 | ||||||
chr3:33134958
|
G | A | 1 | a0001c0005t0084g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1152+693G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134958 | ||||||
chr3:33135022
|
G | C | 1 | a0001c0001t0002g0044 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1152+757G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135022 | ||||||
chr3:33135332
|
A | G | 296 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(293): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1152+1067A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135332 | ||||||
chr3:33135487
|
G | A | 1 | a0001c0001t0065g0311 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1152+1222G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135487 | ||||||
chr3:33135505
|
C | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(65): Show | 88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1152+1240C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135505 | ||||||
chr3:33135510
|
T | C | 9 | a0001c0003t0002g0115a0001c0003t0002g0119a0001c0003t0002g0120others(6): Show | 9 | NA18943.hp1 NA18975.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1152+1245T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135510 | ||||||
chr3:33135581
|
C | T | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+1316C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135581 | ||||||
chr3:33135705
|
G | T | 21 | a0001c0001t0025g0029a0001c0002t0005g0216a0001c0002t0068g0196others(18): Show | 25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+1440G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135705 | ||||||
chr3:33135706
|
T | A | 21 | a0001c0001t0025g0029a0001c0002t0005g0216a0001c0002t0068g0196others(18): Show | 25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+1441T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135706 | ||||||
chr3:33136103
|
T | G | 1 | a0001c0001t0002g0309 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1152+1838T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136103 | ||||||
chr3:33136508
|
T | C | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1152+2243T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136508 | ||||||
chr3:33136550
|
C | T | 295 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(292): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1152+2285C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136550 | ||||||
chr3:33136856
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0093 | 2 | NA18986.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1152+2591G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136856 | ||||||
chr3:33137069
|
C | CT | 66 | a0001c0003t0002g0002a0001c0003t0002g0010a0001c0003t0002g0011others(63): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1152+2814dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33137069 | |||||
chr3:33137114
|
T | C | 1 | a0001c0003t0021g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1152+2849T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137114 | ||||||
chr3:33137204
|
G | A | 72 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(69): Show | 92 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1152+2939G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137204 | ||||||
chr3:33137227
|
G | A | 11 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(8): Show | 11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1152+2962G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137227 | ||||||
chr3:33137262
|
T | C | 295 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(292): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1152+2997T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137262 | ||||||
chr3:33137365
|
T | G | 1 | a0001c0003t0002g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1152+3100T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137365 | ||||||
chr3:33137388
|
G | A | 1 | a0002c0008t0013g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1152+3123G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137388 | ||||||
chr3:33137416
|
C | T | 71 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(68): Show | 91 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1152+3151C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137416 | ||||||
chr3:33137417
|
A | G | 1 | a0001c0004t0073g0072 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1152+3152A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137417 | ||||||
chr3:33137421
|
G | A | 1 | a0001c0003t0002g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1152+3156G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137421 | ||||||
chr3:33137522
|
A | G | 1 | a0001c0003t0014g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1152+3257A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137522 | ||||||
chr3:33137618
|
T | C | 4 | a0001c0001t0028g0081a0001c0001t0028g0082a0001c0001t0057g0083others(1): Show | 4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3353T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137618 | ||||||
chr3:33137832
|
C | T | 1 | a0001c0013t0002g0212 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1152+3567C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137832 | ||||||
chr3:33137982
|
T | G | 4 | a0001c0007t0018g0201a0001c0007t0018g0202a0001c0007t0018g0266others(1): Show | 4 | HG00639.hp2 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+3717T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137982 | ||||||
chr3:33138053
|
G | T | 2 | a0001c0001t0013g0166a0001c0001t0031g0019 | 3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1152+3788G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138053 | ||||||
chr3:33138084
|
T | C | 1 | a0001c0001t0071g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1152+3819T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138084 | ||||||
chr3:33138099
|
C | CT | 17 | a0001c0001t0007g0190a0001c0002t0001g0269a0001c0002t0007g0210others(14): Show | 19 | HG01074.hp2 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1152+3845dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33138099 | |||||
chr3:33138117
|
C | T | 2 | a0001c0005t0026g0279a0001c0005t0026g0280 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1152+3852C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138117 | ||||||
chr3:33138459
|
C | A | 69 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(66): Show | 89 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1153-3936C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138459 | ||||||
chr3:33138491
|
A | T | 72 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(69): Show | 92 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1153-3904A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138491 | ||||||
chr3:33138712
|
A | G | 1 | a0001c0001t0003g0096 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1153-3683A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138712 | ||||||
chr3:33138713
|
G | A | 2 | a0001c0003t0002g0115a0001c0003t0002g0119 | 2 | NA18981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1153-3682G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138713 | ||||||
chr3:33138765
|
G | C | 86 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(83): Show | 106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1153-3630G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138765 | ||||||
chr3:33138932
|
C | T | 2 | a0001c0005t0035g0313a0001c0005t0036g0312 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1153-3463C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138932 | ||||||
chr3:33139059
|
G | A | 4 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(1): Show | 4 | HG00544.hp2 NA18949.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-3336G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139059 | ||||||
chr3:33139093
|
G | A | 1 | a0001c0007t0018g0266 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1153-3302G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139093 | ||||||
chr3:33139152
|
A | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0101others(2): Show | 7 | HG01255.hp1 HG01358.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153-3243A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139152 | ||||||
chr3:33139349
|
C | G | 1 | a0001c0001t0031g0019 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-3046C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139349 | ||||||
chr3:33139378
|
C | T | 4 | a0001c0002t0008g0203a0001c0005t0008g0193a0001c0005t0082g0194others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-3017C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139378 | ||||||
chr3:33139414
|
C | T | 1 | a0002c0008t0013g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1153-2981C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139414 | ||||||
chr3:33139475
|
A | AT | 54 | a0001c0001t0003g0003a0001c0001t0003g0094a0001c0001t0003g0095others(51): Show | 61 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1153-2902dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33139475 | |||||
chr3:33139475
|
AT | A | 7 | a0001c0001t0003g0154a0001c0001t0004g0293a0001c0002t0001g0240others(4): Show | 8 | HG01074.hp1 HG01099.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153-2902delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33139475 | |||||
chr3:33139632
|
A | T | 2 | a0001c0001t0013g0166a0001c0001t0031g0019 | 3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-2763A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139632 | ||||||
chr3:33139639
|
G | C | 2 | a0001c0001t0003g0315a0001c0001t0061g0099 | 2 | NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1153-2756G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139639 | ||||||
chr3:33139677
|
C | T | 1 | a0001c0003t0002g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1153-2718C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139677 | ||||||
chr3:33139693
|
G | A | 1 | a0001c0001t0031g0019 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-2702G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139693 | ||||||
chr3:33139705
|
T | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(83): Show | 108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1153-2690T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139705 | ||||||
chr3:33139768
|
G | A | 1 | a0001c0005t0084g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1153-2627G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139768 | ||||||
chr3:33139848
|
A | G | 93 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(90): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1153-2547A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139848 | ||||||
chr3:33139990
|
T | A | 11 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(8): Show | 11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-2405T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139990 | ||||||
chr3:33140328
|
G | A | 1 | a0005c0015t0005g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1153-2067G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140328 | ||||||
chr3:33140414
|
C | T | 1 | a0001c0001t0086g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153-1981C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140414 | ||||||
chr3:33140560
|
A | C | 87 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0018others(84): Show | 107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1153-1835A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140560 | ||||||
chr3:33140563
|
T | C | 1 | a0001c0002t0001g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1153-1832T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140563 | ||||||
chr3:33140661
|
CA | C | 21 | a0001c0001t0025g0029a0001c0002t0005g0216a0001c0002t0068g0196others(18): Show | 25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1153-1733delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140661 | ||||||
chr3:33140677
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1153-1718T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140677 | ||||||
chr3:33140688
|
T | G | 1 | a0001c0001t0006g0301 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1153-1707T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140688 | ||||||
chr3:33140841
|
G | A | 1 | a0001c0001t0008g0005 | 4 | HG01069.hp1 HG01071.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1554G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140841 | ||||||
chr3:33140863
|
C | T | 1 | a0001c0003t0002g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1153-1532C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140863 | ||||||
chr3:33141002
|
GT | G | 294 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0087others(291): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1153-1384delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33141002 | |||||
chr3:33141037
|
G | A | 2 | a0001c0001t0013g0166a0001c0001t0031g0019 | 3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-1358G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141037 | ||||||
chr3:33141095
|
T | G | 1 | a0001c0006t0006g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153-1300T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141095 | ||||||
chr3:33141240
|
G | C | 6 | a0001c0001t0003g0020a0001c0001t0003g0092a0001c0001t0003g0094others(3): Show | 7 | HG00544.hp1 HG00673.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-1155G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141240 | ||||||
chr3:33141324
|
T | C | 5 | a0001c0001t0019g0159a0001c0004t0019g0070a0001c0005t0019g0197others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-1071T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141324 | ||||||
chr3:33141347
|
A | G | 21 | a0001c0001t0025g0029a0001c0002t0005g0216a0001c0002t0068g0196others(18): Show | 25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1153-1048A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141347 | ||||||
chr3:33141415
|
T | C | 3 | a0002c0008t0013g0049a0002c0008t0013g0050a0002c0008t0013g0191 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1153-980T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141415 | ||||||
chr3:33141456
|
T | C | 1 | a0001c0003t0002g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1153-939T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141456 | ||||||
chr3:33141504
|
A | G | 11 | a0001c0006t0006g0053a0001c0006t0006g0054a0001c0006t0006g0055others(8): Show | 11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-891A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141504 | ||||||
chr3:33141823
|
G | A | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-572G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141823 | ||||||
chr3:33141861
|
C | T | 4 | a0001c0003t0015g0271a0001c0003t0015g0272a0001c0003t0015g0273others(1): Show | 5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-534C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141861 | ||||||
chr3:33142231
|
T | A | 2 | a0002c0008t0013g0049a0002c0008t0013g0050 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1153-164T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33142231 | ||||||
chr3:33142317
|
G | A | 1 | a0002c0008t0013g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1153-78G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33142317 |