geneid | 285343 |
---|---|
ensemblid | ENSG00000179152.20 |
hgncid | 25241 |
symbol | TCAIM |
name | T cell activation inhibitor, mitochondrial |
refseq_nuc | NM_173826.4 |
refseq_prot | NP_776187.2 |
ensembl_nuc | ENST00000342649.9 |
ensembl_prot | ENSP00000341539.4 |
mane_status | MANE Select |
chr | chr3 |
start | 44338766 |
end | 44409448 |
strand | + |
ver | v1.2 |
region | chr3:44338766-44409448 |
region5000 | chr3:44333766-44414448 |
regionname0 | TCAIM_chr3_44338766_44409448 |
regionname5000 | TCAIM_chr3_44333766_44414448 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1491 | 234 | 84 | 55 | 56 | 11 | 26 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
c0002 | 0/0 | 1491 | 5 | 5 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
c0003 | 0/0 | 1491 | 4 | 3 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
c0004 | 0/0 | 1491 | 4 | 0 | 0 | 4 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
c0005 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1880 | 155 | 45 | 36 | 46 | 8 | 19 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0002 | 1/0 | 1880 | 29 | 20 | 7 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0003 | 0/0 | 1881 | 23 | 4 | 6 | 5 | 3 | 5 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0004 | 0/0 | 1864 | 7 | 7 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0005 | 0/0 | 1880 | 6 | 6 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0006 | 0/0 | 1880 | 5 | 0 | 0 | 5 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0007 | 0/0 | 1881 | 4 | 4 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0008 | 0/0 | 1881 | 4 | 1 | 3 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0009 | 0/0 | 1880 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0010 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0011 | 0/0 | 1880 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0012 | 0/0 | 1881 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0013 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0014 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0015 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0016 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0017 | 0/0 | 1880 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0018 | 0/0 | 1881 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0019 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
t0020 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1491 | 234 | 84 | 55 | 56 | 11 | 26 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0003 | 0/0 | 1491 | 4 | 3 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0004 | 0/0 | 1491 | 4 | 0 | 0 | 4 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0005 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0002c0002 | 0/0 | 1491 | 5 | 5 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3370 | 145 | 37 | 35 | 46 | 7 | 19 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0002 | 1/0 | 3370 | 29 | 20 | 7 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0003 | 0/0 | 3371 | 23 | 4 | 6 | 5 | 3 | 5 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0004 | 0/0 | 3354 | 7 | 7 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0005 | 0/0 | 3370 | 6 | 6 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0006 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0007 | 0/0 | 3371 | 4 | 4 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0008 | 0/0 | 3371 | 4 | 1 | 3 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0009 | 0/0 | 3370 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0010 | 0/0 | 3371 | 2 | 2 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0011 | 0/0 | 3370 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0012 | 0/0 | 3371 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0013 | 0/0 | 3370 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0014 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0015 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0016 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0017 | 0/0 | 3370 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0018 | 0/0 | 3371 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0019 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0001t0020 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0003t0001 | 0/0 | 3370 | 4 | 3 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0004t0006 | 0/0 | 3370 | 4 | 0 | 0 | 4 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0001c0005t0001 | 0/0 | 3370 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
a0002c0002t0001 | 0/0 | 3370 | 5 | 5 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | copy fasta | chr3 | 44333766 | 44414448 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0002g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0011g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0013g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0017g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0019g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0001t0020g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0004t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0004t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0004t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0004t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00558 | hp1 | a0001 | c0004 | t0006 | g0168 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00597 | hp2 | a0001 | c0004 | t0006 | g0170 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00639 | hp2 | a0001 | c0001 | t0008 | g0070 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00673 | hp2 | a0001 | c0004 | t0006 | g0169 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0067 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01167 | hp2 | a0001 | c0001 | t0018 | g0215 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0080 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0064 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0063 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0054 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01934 | hp1 | a0001 | c0005 | t0001 | g0135 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02300 | hp2 | a0001 | c0001 | t0013 | g0039 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02630 | hp1 | a0001 | c0001 | t0020 | g0013 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02698 | hp1 | a0001 | c0001 | t0017 | g0158 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0076 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03486 | hp1 | a0001 | c0001 | t0015 | g0008 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0084 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18947 | hp1 | a0001 | c0001 | t0016 | g0228 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18966 | hp2 | a0001 | c0004 | t0006 | g0175 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18986 | hp1 | a0001 | c0001 | t0011 | g0233 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0045 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19091 | hp1 | a0001 | c0001 | t0019 | g0193 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA19091 | hp2 | a0001 | c0001 | t0011 | g0191 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0068 | AFR | ASW | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0093 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | GIH | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0147 | REF | REF | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44407671
|
G | T | 1 | a0002 | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.1480G>T | p.Ala494Ser | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1593/3370 | 1480/1491 | 494/496 | chr3 | 44407671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44367646
|
T | C | 2 | a0001c0003a0002c0002 | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.510T>C | p.Phe170Phe | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/11 | 623/3370 | 510/1491 | 170/496 | chr3 | 44367646 | ||
chr3:44400367
|
T | C | 1 | a0001c0004 | 4 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(1): Show |
synonymous_variant | LOW | c.898T>C | p.Leu300Leu | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/11 | 1011/3370 | 898/1491 | 300/496 | chr3 | 44400367 | ||
chr3:44400534
|
T | C | 1 | a0001c0005 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1065T>C | p.Ser355Ser | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/11 | 1178/3370 | 1065/1491 | 355/496 | chr3 | 44400534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44338768
|
T | C | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(3): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-111T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/11 | 16015 | chr3 | 44338768 | |||||
chr3:44407879
|
C | T | 1 | a0001c0001t0020 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 197 | chr3 | 44407879 | |||||
chr3:44407880
|
G | A | 2 | a0001c0001t0006a0001c0004t0006 | 5 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*198G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 198 | chr3 | 44407880 | |||||
chr3:44407893
|
T | C | 1 | a0001c0001t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 211 | chr3 | 44407893 | |||||
chr3:44408086
|
C | T | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 404 | chr3 | 44408086 | |||||
chr3:44408090
|
A | G | 1 | a0001c0001t0008 | 4 | HG00639.hp2 HG00741.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*408A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 408 | chr3 | 44408090 | |||||
chr3:44408427
|
C | T | 1 | a0001c0001t0004 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*745C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 745 | chr3 | 44408427 | |||||
chr3:44408485
|
C | T | 1 | a0001c0001t0019 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*803C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 803 | chr3 | 44408485 | |||||
chr3:44408579
|
G | GT | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(3): Show | 35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*903dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 904 | INFO_REALIGN_3_PRIME | chr3 | 44408579 | ||||
chr3:44408619
|
G | C | 1 | a0001c0001t0007 | 4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 937 | chr3 | 44408619 | |||||
chr3:44408734
|
A | C | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1052 | chr3 | 44408734 | |||||
chr3:44408781
|
G | A | 1 | a0001c0001t0015 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1099 | chr3 | 44408781 | |||||
chr3:44408808
|
C | T | 1 | a0001c0001t0011 | 2 | NA18986.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1126C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1126 | chr3 | 44408808 | |||||
chr3:44408923
|
C | T | 1 | a0001c0001t0010 | 2 | HG02922.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1241C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1241 | chr3 | 44408923 | |||||
chr3:44409035
|
AGAAAGGA others(9): Show |
A | 1 | a0001c0001t0004 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1357_*1372delAGGA others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1357 | INFO_REALIGN_3_PRIME | chr3 | 44409035 | ||||
chr3:44409059
|
A | G | 1 | a0001c0001t0017 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1377 | chr3 | 44409059 | |||||
chr3:44409072
|
A | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1390A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1390 | chr3 | 44409072 | |||||
chr3:44409184
|
A | G | 1 | a0001c0001t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1502 | chr3 | 44409184 | |||||
chr3:44409211
|
G | A | 1 | a0001c0001t0016 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1529G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1529 | chr3 | 44409211 | |||||
chr3:44409243
|
T | C | 2 | a0001c0001t0005a0001c0001t0015 | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1561T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1561 | chr3 | 44409243 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44338996
|
A | C | 58 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-45+162A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44338996 | ||||||
chr3:44339107
|
C | CAA | 196 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-45+273_-45+274ins others(2): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339107 | ||||||
chr3:44339253
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-45+419C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339253 | ||||||
chr3:44339292
|
G | A | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+458G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339292 | ||||||
chr3:44339378
|
A | G | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+544A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339378 | ||||||
chr3:44339391
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-45+557C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339391 | ||||||
chr3:44339475
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-45+641A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339475 | ||||||
chr3:44339934
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-45+1100T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339934 | ||||||
chr3:44339988
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-45+1154A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339988 | ||||||
chr3:44340418
|
C | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-45+1584C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340418 | ||||||
chr3:44340504
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-45+1670A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340504 | ||||||
chr3:44340553
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-45+1719T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340553 | ||||||
chr3:44340930
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-45+2096T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340930 | ||||||
chr3:44341430
|
A | AT | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+2602dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44341430 | |||||
chr3:44341564
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-45+2730C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341564 | ||||||
chr3:44341645
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-45+2811G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341645 | ||||||
chr3:44341720
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45+2886G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341720 | ||||||
chr3:44341752
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-45+2918A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341752 | ||||||
chr3:44341906
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+3072G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341906 | ||||||
chr3:44342070
|
T | C | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-45+3236T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342070 | ||||||
chr3:44342217
|
C | A | 1 | a0001c0003t0001g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-45+3383C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342217 | ||||||
chr3:44342327
|
G | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-45+3493G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342327 | ||||||
chr3:44342388
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-45+3554C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342388 | ||||||
chr3:44342414
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+3580A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342414 | ||||||
chr3:44342439
|
C | T | 1 | a0001c0003t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-45+3605C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342439 | ||||||
chr3:44342728
|
TA | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+3897delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44342728 | |||||
chr3:44342888
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-45+4054G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342888 | ||||||
chr3:44342999
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-45+4165C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342999 | ||||||
chr3:44343146
|
AAAG | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(13): Show | 16 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+4318_-45+4320d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44343146 | |||||
chr3:44343237
|
C | T | 84 | a0001c0001t0001g0027a0001c0001t0002g0010a0001c0001t0002g0011others(81): Show | 84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+4403C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343237 | ||||||
chr3:44343284
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.-45+4450A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343284 | ||||||
chr3:44343317
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-45+4483A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343317 | ||||||
chr3:44343398
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-45+4564C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343398 | ||||||
chr3:44343499
|
A | G | 84 | a0001c0001t0001g0027a0001c0001t0002g0010a0001c0001t0002g0011others(81): Show | 84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+4665A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343499 | ||||||
chr3:44343582
|
T | A | 1 | a0001c0001t0004g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-45+4748T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343582 | ||||||
chr3:44343621
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+4787C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343621 | ||||||
chr3:44343902
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+5068G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343902 | ||||||
chr3:44344010
|
T | C | 84 | a0001c0001t0001g0027a0001c0001t0002g0010a0001c0001t0002g0011others(81): Show | 84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+5176T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344010 | ||||||
chr3:44344023
|
C | CT | 70 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0144others(67): Show | 71 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-45+5207dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | |||||
chr3:44344023
|
C | CTT | 5 | a0001c0001t0002g0082a0001c0001t0003g0083a0001c0001t0008g0080others(2): Show | 5 | HG01192.hp2 HG02055.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+5206_-45+5207d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | |||||
chr3:44344023
|
CT | C | 92 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-45+5207delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | |||||
chr3:44344040
|
T | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0011g0191 | 3 | NA18981.hp2 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-45+5206T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344040 | ||||||
chr3:44344041
|
T | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0011g0191 | 3 | NA18981.hp2 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-45+5207T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344041 | ||||||
chr3:44344066
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0019g0193 | 3 | HG02080.hp1 HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-45+5232G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344066 | ||||||
chr3:44344213
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-45+5379T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344213 | ||||||
chr3:44344291
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-45+5457C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344291 | ||||||
chr3:44344322
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.-45+5488G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344322 | ||||||
chr3:44344771
|
G | A | 1 | a0001c0001t0008g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-45+5937G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344771 | ||||||
chr3:44344813
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.-45+5979G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344813 | ||||||
chr3:44344906
|
A | G | 38 | a0001c0001t0001g0027a0001c0001t0003g0047a0001c0001t0003g0048others(35): Show | 38 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.-45+6072A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344906 | ||||||
chr3:44344998
|
C | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+6164C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344998 | ||||||
chr3:44345103
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-45+6269A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345103 | ||||||
chr3:44345122
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-45+6288C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345122 | ||||||
chr3:44345141
|
G | A | 4 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+6307G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345141 | ||||||
chr3:44345154
|
G | A | 5 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+6320G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345154 | ||||||
chr3:44345205
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-45+6371G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345205 | ||||||
chr3:44345282
|
T | C | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-45+6448T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345282 | ||||||
chr3:44345843
|
C | G | 1 | a0001c0001t0002g0046 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-45+7009C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345843 | ||||||
chr3:44346080
|
C | T | 1 | a0001c0001t0003g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-45+7246C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346080 | ||||||
chr3:44346103
|
TAAAAGTA | T | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+7270_-45+7276d others(9): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346103 | ||||||
chr3:44346148
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-45+7314G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346148 | ||||||
chr3:44346292
|
A | G | 1 | a0001c0001t0004g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-45+7458A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346292 | ||||||
chr3:44346350
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-45+7516C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346350 | ||||||
chr3:44346436
|
A | G | 4 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+7602A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346436 | ||||||
chr3:44346609
|
G | A | 4 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+7775G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346609 | ||||||
chr3:44346644
|
C | G | 1 | a0002c0002t0001g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-45+7810C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346644 | ||||||
chr3:44347094
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-44-7645G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347094 | ||||||
chr3:44347164
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-44-7575C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347164 | ||||||
chr3:44347168
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0243 | 2 | HG02056.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-44-7571A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347168 | ||||||
chr3:44347400
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(165): Show | 170 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-44-7339A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347400 | ||||||
chr3:44347448
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-7291G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347448 | ||||||
chr3:44347505
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0146others(33): Show | 37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.-44-7234A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347505 | ||||||
chr3:44347710
|
C | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-7029C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347710 | ||||||
chr3:44348042
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-44-6697A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348042 | ||||||
chr3:44348293
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-6446G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348293 | ||||||
chr3:44348703
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-44-6036G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348703 | ||||||
chr3:44348771
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44-5968C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348771 | ||||||
chr3:44348791
|
G | C | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-5948G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348791 | ||||||
chr3:44348953
|
G | A | 18 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053others(15): Show | 18 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44-5786G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348953 | ||||||
chr3:44349013
|
AG | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 5 | HG01358.hp1 HG01975.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-5725delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349013 | ||||||
chr3:44349127
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-44-5612G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349127 | ||||||
chr3:44349234
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44-5505G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349234 | ||||||
chr3:44349566
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-44-5173A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349566 | ||||||
chr3:44349614
|
A | G | 1 | a0001c0005t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-5125A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349614 | ||||||
chr3:44349693
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG01106.hp1 HG02257.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-5046G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349693 | ||||||
chr3:44349773
|
G | A | 2 | a0001c0001t0003g0051a0001c0001t0003g0083 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-44-4966G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349773 | ||||||
chr3:44349849
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-44-4890G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349849 | ||||||
chr3:44349850
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-44-4889T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349850 | ||||||
chr3:44349937
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-44-4802G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349937 | ||||||
chr3:44350077
|
A | G | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-4662A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350077 | ||||||
chr3:44350161
|
T | C | 2 | a0001c0001t0007g0065a0001c0001t0007g0066 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-44-4578T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350161 | ||||||
chr3:44350200
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-44-4539G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350200 | ||||||
chr3:44350245
|
G | T | 1 | a0001c0001t0001g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-44-4494G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350245 | ||||||
chr3:44350403
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-44-4336C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350403 | ||||||
chr3:44350496
|
G | A | 1 | a0001c0005t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-4243G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350496 | ||||||
chr3:44350815
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0194 | 2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-44-3924G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350815 | ||||||
chr3:44350816
|
A | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0194 | 2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-44-3923A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350816 | ||||||
chr3:44350887
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-44-3852T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350887 | ||||||
chr3:44350908
|
G | T | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44-3831G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350908 | ||||||
chr3:44351066
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-3673G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351066 | ||||||
chr3:44351192
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44-3547T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351192 | ||||||
chr3:44351241
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-44-3498G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351241 | ||||||
chr3:44351258
|
G | T | 1 | a0001c0001t0003g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44-3481G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351258 | ||||||
chr3:44351264
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-44-3475C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351264 | ||||||
chr3:44351293
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-44-3446G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351293 | ||||||
chr3:44351347
|
G | GT | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-3381dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44351347 | |||||
chr3:44351382
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-44-3357T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351382 | ||||||
chr3:44351628
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-44-3111G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351628 | ||||||
chr3:44351629
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-44-3110G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351629 | ||||||
chr3:44351644
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-44-3095A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351644 | ||||||
chr3:44351815
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-2924G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351815 | ||||||
chr3:44352087
|
G | GTA | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-2638_-44-2637d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352087 | |||||
chr3:44352087
|
GTA | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-2638_-44-2637d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352087 | |||||
chr3:44352179
|
C | T | 4 | a0001c0001t0007g0065a0001c0001t0007g0066a0001c0001t0007g0074others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-2560C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352179 | ||||||
chr3:44352419
|
G | A | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-2320G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352419 | ||||||
chr3:44352641
|
A | G | 1 | a0001c0003t0001g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-44-2098A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352641 | ||||||
chr3:44352660
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-44-2079G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352660 | ||||||
chr3:44352923
|
C | CT | 8 | a0001c0001t0002g0011a0001c0001t0004g0086a0001c0001t0004g0087others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-1800dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | |||||
chr3:44352923
|
C | CTTT | 102 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-44-1802_-44-1800d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | |||||
chr3:44352923
|
C | CTTTT | 7 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0127others(4): Show | 8 | HG00741.hp1 HG01099.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-1803_-44-1800d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | |||||
chr3:44352923
|
CT | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0154a0001c0001t0001g0156others(2): Show | 5 | HG02896.hp1 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1800delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | |||||
chr3:44352955
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0020g0013 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-44-1784C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352955 | ||||||
chr3:44352956
|
G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-44-1783G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352956 | ||||||
chr3:44353092
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44-1647G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353092 | ||||||
chr3:44353163
|
C | G | 1 | a0001c0001t0004g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-1576C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353163 | ||||||
chr3:44353233
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44-1506T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353233 | ||||||
chr3:44353237
|
TAGTATC | T | 101 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-44-1501_-44-1496d others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353237 | ||||||
chr3:44353395
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-44-1344T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353395 | ||||||
chr3:44353404
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-44-1335T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353404 | ||||||
chr3:44354044
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049 | 3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-695A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354044 | ||||||
chr3:44354073
|
A | C | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-666A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354073 | ||||||
chr3:44354128
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-44-611G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354128 | ||||||
chr3:44354324
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.-44-415G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354324 | ||||||
chr3:44354420
|
T | C | 1 | a0001c0005t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-319T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354420 | ||||||
chr3:44354915
|
T | C | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.29+104T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44354915 | ||||||
chr3:44355194
|
C | A | 3 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085 | 3 | HG02572.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.29+383C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355194 | ||||||
chr3:44355246
|
TA | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.29+440delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44355246 | |||||
chr3:44355646
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0053 | 2 | HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.29+835G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355646 | ||||||
chr3:44355676
|
G | A | 1 | a0001c0001t0008g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29+865G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355676 | ||||||
chr3:44355732
|
A | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.29+921A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355732 | ||||||
chr3:44355797
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0177 | 2 | NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.29+986A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355797 | ||||||
chr3:44355830
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.29+1019C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355830 | ||||||
chr3:44355878
|
T | C | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.29+1067T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355878 | ||||||
chr3:44355955
|
G | C | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.29+1144G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355955 | ||||||
chr3:44355968
|
G | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.29+1157G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355968 | ||||||
chr3:44356217
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.29+1406G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356217 | ||||||
chr3:44356295
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0145others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.30-1446G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356295 | ||||||
chr3:44356336
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.30-1405G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356336 | ||||||
chr3:44356653
|
G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.30-1088G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356653 | ||||||
chr3:44356693
|
TG | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.30-1046delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44356693 | |||||
chr3:44356736
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0145others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.30-1005C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356736 | ||||||
chr3:44356779
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.30-962A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356779 | ||||||
chr3:44356811
|
C | CA | 23 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(20): Show | 23 | HG00738.hp1 HG01192.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.30-914dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44356811 | |||||
chr3:44356824
|
A | AC | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.30-917_30-916insC | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356824 | ||||||
chr3:44356869
|
G | A | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.30-872G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356869 | ||||||
chr3:44356923
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.30-818G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356923 | ||||||
chr3:44356930
|
A | G | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.30-811A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356930 | ||||||
chr3:44357019
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.30-722A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357019 | ||||||
chr3:44357129
|
G | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(99): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.30-612G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357129 | ||||||
chr3:44357343
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30-398C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357343 | ||||||
chr3:44357393
|
A | AAGAG | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.30-346_30-343dupGA others(2): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44357393 | |||||
chr3:44357434
|
A | G | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30-307A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357434 | ||||||
chr3:44357616
|
A | G | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.30-125A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357616 | ||||||
chr3:44358176
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.165+300T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358176 | ||||||
chr3:44358488
|
A | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.165+612A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358488 | ||||||
chr3:44358669
|
G | C | 1 | a0001c0005t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.165+793G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358669 | ||||||
chr3:44358739
|
A | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.165+863A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358739 | ||||||
chr3:44359155
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.165+1279G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359155 | ||||||
chr3:44359169
|
T | C | 18 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053others(15): Show | 18 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+1293T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359169 | ||||||
chr3:44359763
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(99): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.166-1602C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359763 | ||||||
chr3:44359869
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-1496G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359869 | ||||||
chr3:44360011
|
C | G | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-1354C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360011 | ||||||
chr3:44360153
|
C | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-1212C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360153 | ||||||
chr3:44360440
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.166-925G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360440 | ||||||
chr3:44360571
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.166-794G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360571 | ||||||
chr3:44360761
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.166-604G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360761 | ||||||
chr3:44360772
|
A | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.166-593A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360772 | ||||||
chr3:44360809
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.166-556C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360809 | ||||||
chr3:44360882
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-483A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360882 | ||||||
chr3:44360899
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.166-466C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360899 | ||||||
chr3:44361599
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.319+81T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44361599 | ||||||
chr3:44361875
|
A | G | 2 | a0001c0001t0009g0063a0001c0001t0009g0064 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.319+357A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44361875 | ||||||
chr3:44362200
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.319+682A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362200 | ||||||
chr3:44362259
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319+741C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362259 | ||||||
chr3:44362387
|
C | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+869C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362387 | ||||||
chr3:44362700
|
C | T | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1182C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362700 | ||||||
chr3:44362909
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319+1391A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362909 | ||||||
chr3:44363037
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0178 | 3 | HG02257.hp2 HG04199.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.319+1519C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363037 | ||||||
chr3:44363229
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.319+1711T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363229 | ||||||
chr3:44363563
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.319+2045A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363563 | ||||||
chr3:44363655
|
A | C | 3 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0062 | 3 | HG00423.hp2 HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.319+2137A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363655 | ||||||
chr3:44363920
|
C | CT | 23 | a0001c0001t0001g0027a0001c0001t0002g0016a0001c0001t0002g0025others(20): Show | 23 | HG00423.hp2 HG00741.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+2429dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
C | CTT | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+2428_319+2429d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
C | CTTT | 6 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0177others(3): Show | 6 | HG02258.hp1 HG02698.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+2427_319+2429d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
C | CTTTT | 22 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0148others(19): Show | 23 | HG00558.hp1 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.319+2426_319+2429d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
C | CTTTTT | 14 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 14 | HG00597.hp2 HG00642.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+2425_319+2429d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.319+2420_319+2429d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
CT | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0094a0001c0001t0001g0096others(19): Show | 22 | HG00423.hp1 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.319+2429delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363920
|
CTT | C | 92 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.319+2428_319+2429d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | |||||
chr3:44363951
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(110): Show | 114 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.319+2433A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363951 | ||||||
chr3:44363975
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.319+2457T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363975 | ||||||
chr3:44364118
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2600G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364118 | ||||||
chr3:44364162
|
C | G | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319+2644C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364162 | ||||||
chr3:44364212
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.319+2694C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364212 | ||||||
chr3:44364212
|
C | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2694C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364212 | ||||||
chr3:44364239
|
T | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 9 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+2721T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364239 | ||||||
chr3:44364275
|
T | A | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319+2757T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364275 | ||||||
chr3:44364410
|
T | C | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.319+2892T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364410 | ||||||
chr3:44364627
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.320-2829C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364627 | ||||||
chr3:44364745
|
C | CA | 19 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0159others(16): Show | 19 | HG00597.hp2 HG01109.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-2694dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44364745 | |||||
chr3:44364784
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.320-2672C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364784 | ||||||
chr3:44364913
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.320-2543A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364913 | ||||||
chr3:44365051
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.320-2405T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365051 | ||||||
chr3:44365116
|
TTTTTC | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.320-2337_320-2333d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44365116 | |||||
chr3:44365334
|
C | CT | 6 | a0001c0001t0001g0098a0001c0001t0001g0126a0001c0001t0001g0130others(3): Show | 6 | HG01358.hp1 HG01975.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-2109dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44365334 | |||||
chr3:44365409
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.320-2047A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365409 | ||||||
chr3:44365489
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.320-1967C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365489 | ||||||
chr3:44365618
|
G | T | 5 | a0001c0001t0006g0174a0001c0004t0006g0168a0001c0004t0006g0169others(2): Show | 5 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-1838G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365618 | ||||||
chr3:44365754
|
C | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1702C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365754 | ||||||
chr3:44365917
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.320-1539T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365917 | ||||||
chr3:44365948
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.320-1508C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365948 | ||||||
chr3:44366218
|
AT | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.320-1232delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366218 | |||||
chr3:44366463
|
G | GT | 28 | a0001c0001t0001g0027a0001c0001t0001g0129a0001c0001t0001g0130others(25): Show | 28 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.320-973dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366463 | |||||
chr3:44366463
|
GT | G | 89 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.320-973delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366463 | |||||
chr3:44366472
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.320-984T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366472 | ||||||
chr3:44366529
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.320-927G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366529 | ||||||
chr3:44366605
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-851C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366605 | ||||||
chr3:44366627
|
AT | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(157): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.320-817delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366627 | |||||
chr3:44366709
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.320-747G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366709 | ||||||
chr3:44366763
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.320-693G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366763 | ||||||
chr3:44366802
|
G | A | 4 | a0001c0001t0007g0065a0001c0001t0007g0066a0001c0001t0007g0074others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-654G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366802 | ||||||
chr3:44366905
|
T | G | 100 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.320-551T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366905 | ||||||
chr3:44366978
|
T | C | 1 | a0001c0001t0004g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.320-478T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366978 | ||||||
chr3:44367349
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.320-107C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44367349 | ||||||
chr3:44367372
|
G | GT | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.320-81dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44367372 | |||||
chr3:44367958
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.572+250T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44367958 | ||||||
chr3:44367984
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.572+276T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44367984 | ||||||
chr3:44368097
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+389C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368097 | ||||||
chr3:44368111
|
G | A | 1 | a0001c0001t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.572+403G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368111 | ||||||
chr3:44368154
|
T | C | 37 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(34): Show | 37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+446T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368154 | ||||||
chr3:44368581
|
T | C | 1 | a0001c0001t0011g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.572+873T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368581 | ||||||
chr3:44369015
|
C | T | 1 | a0001c0004t0006g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.572+1307C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369015 | ||||||
chr3:44369374
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0146others(33): Show | 37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+1666G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369374 | ||||||
chr3:44369708
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.572+2000C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369708 | ||||||
chr3:44369942
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+2234G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369942 | ||||||
chr3:44370076
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.572+2368G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370076 | ||||||
chr3:44370083
|
ATTC | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.572+2378_572+2380d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370083 | |||||
chr3:44370287
|
C | G | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.572+2579C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370287 | ||||||
chr3:44370380
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.572+2672G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370380 | ||||||
chr3:44370413
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572+2705G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370413 | ||||||
chr3:44370455
|
C | CA | 71 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0108others(68): Show | 72 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.572+2764dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | |||||
chr3:44370455
|
C | CAA | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(4): Show | 7 | HG00597.hp2 HG01175.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+2763_572+2764d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | |||||
chr3:44370455
|
CA | C | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+2764delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | |||||
chr3:44370618
|
T | C | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+2910T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370618 | ||||||
chr3:44370641
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.572+2933C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370641 | ||||||
chr3:44370669
|
T | TG | 5 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02486.hp2 HG02735.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+2961_572+2962i others(3): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370669 | ||||||
chr3:44370670
|
T | G | 32 | a0001c0001t0001g0194a0001c0001t0003g0050a0001c0001t0003g0051others(29): Show | 32 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.572+2962T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370670 | ||||||
chr3:44370716
|
G | A | 5 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+3008G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370716 | ||||||
chr3:44370750
|
C | CT | 37 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(34): Show | 37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+3045dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370750 | |||||
chr3:44370751
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+3043T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370751 | ||||||
chr3:44370752
|
TTC | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.572+3046_572+3047d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370752 | |||||
chr3:44370753
|
TC | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0130a0001c0001t0001g0145 | 3 | HG02647.hp1 HG02818.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.572+3046delC | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370753 | ||||||
chr3:44370754
|
C | T | 55 | a0001c0001t0001g0027a0001c0001t0002g0037a0001c0001t0003g0047others(52): Show | 55 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.572+3046C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370754 | ||||||
chr3:44370908
|
A | AT | 115 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.572+3220dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | |||||
chr3:44370908
|
A | ATT | 6 | a0001c0001t0001g0095a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+3219_572+3220d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | |||||
chr3:44370908
|
AT | A | 10 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(7): Show | 10 | HG01516.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.572+3220delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | |||||
chr3:44370972
|
C | T | 1 | a0001c0001t0019g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.572+3264C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370972 | ||||||
chr3:44370998
|
G | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0040others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+3290G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370998 | ||||||
chr3:44371062
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.572+3354G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371062 | ||||||
chr3:44371154
|
C | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+3446C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371154 | ||||||
chr3:44371205
|
C | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+3497C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371205 | ||||||
chr3:44372004
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0004g0086a0001c0001t0004g0087others(7): Show | 10 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+4296A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372004 | ||||||
chr3:44372006
|
G | A | 9 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+4298G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372006 | ||||||
chr3:44372009
|
A | AGAAG | 6 | a0001c0001t0002g0011a0001c0001t0002g0023a0001c0001t0002g0033others(3): Show | 6 | HG02300.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+4366_572+4369d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
A | AGAAGGAA others(5): Show |
1 | a0001c0001t0002g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.572+4358_572+4369d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
AGAAG | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0001g0099others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.572+4366_572+4369d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
AGAAGGAA others(1): Show |
A | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(29): Show | 33 | HG00423.hp1 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.572+4362_572+4369d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
AGAAGGAA others(5): Show |
A | 24 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0109others(21): Show | 24 | HG01099.hp2 HG01123.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.572+4358_572+4369d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
AGAAGGAA others(9): Show |
A | 8 | a0001c0001t0001g0108a0001c0001t0001g0129a0001c0001t0001g0190others(5): Show | 8 | HG00738.hp1 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+4354_572+4369d others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372009
|
AGAAGGAA others(13): Show |
A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0004t0006g0169 | 3 | HG00673.hp2 HG02922.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.572+4350_572+4369d others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | |||||
chr3:44372011
|
AAGGAAGG others(7): Show |
A | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+4304_572+4317d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372011 | ||||||
chr3:44372011
|
AAGGAAGG others(11): Show |
A | 1 | a0001c0001t0004g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.572+4304_572+4321d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372011 | ||||||
chr3:44372040
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.572+4332A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372040 | ||||||
chr3:44372053
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.572+4345G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372053 | ||||||
chr3:44372064
|
A | AGGAAGGA others(13): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.572+4369_572+4370i others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | |||||
chr3:44372064
|
A | AGGAAGGA others(9): Show |
1 | a0001c0001t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.572+4369_572+4370i others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | |||||
chr3:44372064
|
A | AGGAAGGA others(5): Show |
7 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0177others(4): Show | 7 | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+4367_572+4368i others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | |||||
chr3:44372064
|
A | AGGAAGGA others(1): Show |
6 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00609.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+4363_572+4364i others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | |||||
chr3:44372064
|
A | AGGAG | 13 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(10): Show | 13 | HG00642.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.572+4359_572+4360i others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | |||||
chr3:44372064
|
A | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0145others(17): Show | 21 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.572+4356A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372064 | ||||||
chr3:44372077
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0027others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.572+4369G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | ||||||
chr3:44372077
|
G | GGAAC | 21 | a0001c0001t0001g0100a0001c0001t0001g0196a0001c0001t0001g0218others(18): Show | 21 | HG01123.hp2 HG01261.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.572+4369_572+4370i others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | ||||||
chr3:44372077
|
G | GGAAGGAA others(9): Show |
1 | a0002c0002t0001g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.572+4369_572+4370i others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | ||||||
chr3:44372120
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.572+4412C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372120 | ||||||
chr3:44372134
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0202 | 2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.572+4426C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372134 | ||||||
chr3:44372197
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.572+4489G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372197 | ||||||
chr3:44372337
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.572+4629A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372337 | ||||||
chr3:44372511
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.572+4803T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372511 | ||||||
chr3:44372566
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.572+4858C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372566 | ||||||
chr3:44372570
|
C | G | 2 | a0001c0003t0001g0026a0001c0003t0001g0085 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.572+4862C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372570 | ||||||
chr3:44372587
|
C | CT | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+4893dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372587 | |||||
chr3:44372632
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+4924C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372632 | ||||||
chr3:44372793
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.572+5085G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372793 | ||||||
chr3:44373115
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+5414_572+5437d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44373115 | |||||
chr3:44373416
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.572+5708G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373416 | ||||||
chr3:44373492
|
TA | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(157): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.572+5797delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44373492 | |||||
chr3:44373609
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+5901G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373609 | ||||||
chr3:44373746
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+6038T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373746 | ||||||
chr3:44374281
|
GCTTT | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0142others(40): Show | 44 | HG00609.hp1 HG00642.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.572+6578_572+6581d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374281 | |||||
chr3:44374282
|
CTTTCT | C | 6 | a0001c0001t0001g0141a0001c0001t0006g0174a0001c0004t0006g0168others(3): Show | 6 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+6578_572+6582d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374282 | |||||
chr3:44374286
|
C | CT | 39 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0134others(36): Show | 39 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.572+6593dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374286 | |||||
chr3:44374286
|
CT | C | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(9): Show | 12 | HG00642.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.572+6593delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374286 | |||||
chr3:44374393
|
G | A | 5 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+6685G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374393 | ||||||
chr3:44374420
|
T | C | 101 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.572+6712T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374420 | ||||||
chr3:44374494
|
A | G | 37 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(34): Show | 37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+6786A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374494 | ||||||
chr3:44374860
|
A | G | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+7152A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374860 | ||||||
chr3:44375015
|
A | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+7307A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375015 | ||||||
chr3:44375373
|
A | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049 | 3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.572+7665A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375373 | ||||||
chr3:44375429
|
G | A | 2 | a0001c0003t0001g0026a0001c0003t0001g0085 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.572+7721G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375429 | ||||||
chr3:44375455
|
A | T | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.572+7747A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375455 | ||||||
chr3:44375535
|
G | C | 101 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.572+7827G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375535 | ||||||
chr3:44375563
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.572+7855T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375563 | ||||||
chr3:44375737
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.572+8029C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375737 | ||||||
chr3:44375745
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.572+8037T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375745 | ||||||
chr3:44375977
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+8269G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375977 | ||||||
chr3:44376024
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.572+8316G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376024 | ||||||
chr3:44376089
|
T | C | 1 | a0001c0001t0007g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572+8381T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376089 | ||||||
chr3:44376242
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.572+8534T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376242 | ||||||
chr3:44376320
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+8612A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376320 | ||||||
chr3:44376498
|
T | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0166 | 2 | HG02135.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.572+8790T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376498 | ||||||
chr3:44376572
|
A | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+8864A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376572 | ||||||
chr3:44376625
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+8917A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376625 | ||||||
chr3:44376870
|
C | T | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+9162C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376870 | ||||||
chr3:44377045
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.572+9337A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377045 | ||||||
chr3:44377161
|
C | T | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+9453C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377161 | ||||||
chr3:44377200
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.572+9492A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377200 | ||||||
chr3:44377342
|
C | G | 5 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+9634C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377342 | ||||||
chr3:44377391
|
T | C | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.572+9683T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377391 | ||||||
chr3:44377404
|
AGAAAGTT others(11): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572+9698_572+9715d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44377404 | |||||
chr3:44377581
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.572+9873G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377581 | ||||||
chr3:44377742
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+10034G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377742 | ||||||
chr3:44378249
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.572+10541C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378249 | ||||||
chr3:44378391
|
C | G | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.572+10683C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378391 | ||||||
chr3:44378459
|
C | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.572+10751C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378459 | ||||||
chr3:44378546
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.572+10838G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378546 | ||||||
chr3:44378586
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.572+10878G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378586 | ||||||
chr3:44378643
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.572+10935C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378643 | ||||||
chr3:44378746
|
G | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0145others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.572+11038G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378746 | ||||||
chr3:44378754
|
T | C | 5 | a0001c0001t0003g0054a0001c0001t0003g0056a0001c0001t0003g0057others(2): Show | 5 | HG00733.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+11046T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378754 | ||||||
chr3:44378760
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.572+11052G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378760 | ||||||
chr3:44378784
|
G | A | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+11076G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378784 | ||||||
chr3:44378796
|
C | CA | 59 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0118others(56): Show | 59 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.572+11103dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44378796 | |||||
chr3:44378796
|
C | CAA | 4 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 5 | HG01358.hp1 HG01975.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+11102_572+1110 others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44378796 | |||||
chr3:44378813
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.572+11105G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378813 | ||||||
chr3:44379206
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11498T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379206 | ||||||
chr3:44379206
|
TAATA | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0172a0001c0001t0001g0176 | 3 | HG01175.hp2 HG02683.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.572+11508_572+1151 others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44379206 | |||||
chr3:44379270
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.572+11562G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379270 | ||||||
chr3:44379274
|
G | C | 1 | a0001c0001t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+11566G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379274 | ||||||
chr3:44379294
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+11586A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379294 | ||||||
chr3:44379482
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+11774A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379482 | ||||||
chr3:44379501
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11793G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379501 | ||||||
chr3:44379618
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11910C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379618 | ||||||
chr3:44379672
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.572+11964T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379672 | ||||||
chr3:44379825
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG01123.hp2 HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.572+12117G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379825 | ||||||
chr3:44379988
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG00438.hp1 HG02040.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.572+12280C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379988 | ||||||
chr3:44380391
|
A | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.573-12464A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380391 | ||||||
chr3:44380430
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.573-12425A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380430 | ||||||
chr3:44380487
|
T | C | 1 | a0001c0005t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.573-12368T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380487 | ||||||
chr3:44381262
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-11593C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381262 | ||||||
chr3:44381744
|
A | G | 1 | a0001c0001t0016g0228 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.573-11111A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381744 | ||||||
chr3:44381924
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.573-10931C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381924 | ||||||
chr3:44381959
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.573-10896A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381959 | ||||||
chr3:44381973
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.573-10882T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381973 | ||||||
chr3:44381976
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573-10879G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381976 | ||||||
chr3:44382179
|
G | A | 11 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0207others(8): Show | 11 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.573-10676G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382179 | ||||||
chr3:44382312
|
C | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.573-10543C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382312 | ||||||
chr3:44382440
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0185 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.573-10415A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382440 | ||||||
chr3:44382536
|
A | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-10319A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382536 | ||||||
chr3:44382566
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0126others(2): Show | 5 | HG00735.hp1 HG01934.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-10289A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382566 | ||||||
chr3:44382692
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.573-10163G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382692 | ||||||
chr3:44382734
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573-10121A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382734 | ||||||
chr3:44382873
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.573-9982A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382873 | ||||||
chr3:44383117
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-9738G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383117 | ||||||
chr3:44383187
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.573-9668C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383187 | ||||||
chr3:44383347
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.573-9508C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383347 | ||||||
chr3:44383475
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573-9380T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383475 | ||||||
chr3:44383536
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.573-9319A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383536 | ||||||
chr3:44383557
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573-9298C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383557 | ||||||
chr3:44383641
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.573-9214A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383641 | ||||||
chr3:44383685
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.573-9170G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383685 | ||||||
chr3:44383690
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-9165G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383690 | ||||||
chr3:44383809
|
C | CA | 5 | a0001c0001t0002g0023a0001c0001t0002g0036a0001c0001t0005g0004others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-9021dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | |||||
chr3:44383809
|
C | CAAAA | 6 | a0001c0001t0020g0013a0001c0003t0001g0014a0002c0002t0001g0028others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-9024_573-9021d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | |||||
chr3:44383809
|
CA | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0109others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-9021delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | |||||
chr3:44383809
|
CAA | C | 96 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.573-9022_573-9021d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | |||||
chr3:44383809
|
CAAAAA | C | 35 | a0001c0001t0001g0027a0001c0001t0003g0047a0001c0001t0003g0048others(32): Show | 35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.573-9025_573-9021d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | |||||
chr3:44383935
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.573-8920G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383935 | ||||||
chr3:44383947
|
A | G | 1 | a0001c0001t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.573-8908A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383947 | ||||||
chr3:44384343
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-8512G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384343 | ||||||
chr3:44384499
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(111): Show | 115 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.573-8356C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384499 | ||||||
chr3:44384546
|
G | C | 1 | a0001c0001t0018g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.573-8309G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384546 | ||||||
chr3:44384587
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-8268A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384587 | ||||||
chr3:44384634
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.573-8221C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384634 | ||||||
chr3:44384808
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-8047A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384808 | ||||||
chr3:44385542
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.573-7313C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385542 | ||||||
chr3:44385544
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-7311G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385544 | ||||||
chr3:44385600
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-7255G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385600 | ||||||
chr3:44386209
|
C | CA | 76 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0096others(73): Show | 77 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.573-6623dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | |||||
chr3:44386209
|
C | CAA | 39 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0140others(36): Show | 39 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.573-6624_573-6623d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | |||||
chr3:44386209
|
C | CAAA | 9 | a0001c0001t0001g0002a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 10 | HG01106.hp1 HG01175.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.573-6625_573-6623d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | |||||
chr3:44386479
|
C | T | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-6376C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386479 | ||||||
chr3:44386621
|
G | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0224 | 2 | HG01261.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.573-6234G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386621 | ||||||
chr3:44386641
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0121a0001c0001t0001g0132 | 3 | HG00642.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.573-6214C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386641 | ||||||
chr3:44386724
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.573-6131C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386724 | ||||||
chr3:44386738
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(99): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.573-6117T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386738 | ||||||
chr3:44386929
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-5926G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386929 | ||||||
chr3:44386945
|
C | T | 100 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.573-5910C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386945 | ||||||
chr3:44386954
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(99): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.573-5901G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386954 | ||||||
chr3:44386955
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.573-5900T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386955 | ||||||
chr3:44386993
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.573-5862C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386993 | ||||||
chr3:44386994
|
G | A | 6 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0040others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-5861G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386994 | ||||||
chr3:44387319
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0145others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.573-5536C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387319 | ||||||
chr3:44387430
|
AG | A | 6 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-5422delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44387430 | |||||
chr3:44387643
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573-5212C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387643 | ||||||
chr3:44387953
|
T | G | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573-4902T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387953 | ||||||
chr3:44387968
|
A | T | 1 | a0001c0003t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573-4887A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387968 | ||||||
chr3:44388022
|
A | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0173a0001c0001t0001g0207others(2): Show | 5 | HG00597.hp2 HG02148.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-4833A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388022 | ||||||
chr3:44388200
|
T | C | 2 | a0001c0001t0007g0065a0001c0001t0007g0066 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.573-4655T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388200 | ||||||
chr3:44388441
|
TAGAGTC | T | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-4408_573-4403d others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44388441 | |||||
chr3:44388694
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.573-4161G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388694 | ||||||
chr3:44388840
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0146others(39): Show | 43 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.573-4015G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388840 | ||||||
chr3:44388998
|
T | G | 1 | a0001c0001t0015g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.573-3857T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388998 | ||||||
chr3:44389029
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573-3826C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389029 | ||||||
chr3:44389042
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-3813G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389042 | ||||||
chr3:44389222
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-3633G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389222 | ||||||
chr3:44389503
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.573-3352G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389503 | ||||||
chr3:44389688
|
G | A | 4 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-3167G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389688 | ||||||
chr3:44389746
|
T | TA | 108 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.573-3097dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44389746 | |||||
chr3:44390069
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0132 | 2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.573-2786A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390069 | ||||||
chr3:44390148
|
A | G | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.573-2707A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390148 | ||||||
chr3:44390707
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.573-2148A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390707 | ||||||
chr3:44390737
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0146others(33): Show | 37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.573-2118G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390737 | ||||||
chr3:44390878
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-1977C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390878 | ||||||
chr3:44390891
|
A | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0172a0001c0001t0001g0176others(1): Show | 4 | HG01175.hp2 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-1964A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390891 | ||||||
chr3:44391113
|
G | A | 1 | a0001c0001t0004g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.573-1742G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391113 | ||||||
chr3:44391218
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-1637G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391218 | ||||||
chr3:44391274
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.573-1581C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391274 | ||||||
chr3:44391338
|
G | A | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-1517G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391338 | ||||||
chr3:44391339
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.573-1516C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391339 | ||||||
chr3:44391345
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.573-1510C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391345 | ||||||
chr3:44391358
|
T | A | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573-1497T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391358 | ||||||
chr3:44391394
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.573-1461A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391394 | ||||||
chr3:44391748
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.573-1107A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391748 | ||||||
chr3:44391990
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573-865A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391990 | ||||||
chr3:44392075
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.573-780T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392075 | ||||||
chr3:44392145
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG02818.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.573-710A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392145 | ||||||
chr3:44392282
|
G | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.573-573G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392282 | ||||||
chr3:44392418
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.573-437C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392418 | ||||||
chr3:44392766
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573-89G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392766 | ||||||
chr3:44392819
|
G | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0033a0001c0001t0002g0035others(5): Show | 8 | HG01123.hp1 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.573-36G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392819 | ||||||
chr3:44393182
|
G | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.695+205G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393182 | ||||||
chr3:44393183
|
C | T | 36 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(33): Show | 36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.695+206C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393183 | ||||||
chr3:44393348
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695+371C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393348 | ||||||
chr3:44393618
|
C | T | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+641C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393618 | ||||||
chr3:44393743
|
C | T | 2 | a0001c0001t0003g0072a0001c0001t0003g0077 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.695+766C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393743 | ||||||
chr3:44393788
|
A | G | 101 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.695+811A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393788 | ||||||
chr3:44394066
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.695+1089T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394066 | ||||||
chr3:44394110
|
CT | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.695+1141delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394110 | |||||
chr3:44394185
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.695+1208G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394185 | ||||||
chr3:44394346
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+1369A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394346 | ||||||
chr3:44394365
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.695+1388A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394365 | ||||||
chr3:44394401
|
G | A | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+1424G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394401 | ||||||
chr3:44394419
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.695+1442G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394419 | ||||||
chr3:44394557
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695+1580A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394557 | ||||||
chr3:44394618
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+1641G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394618 | ||||||
chr3:44394666
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.695+1689C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394666 | ||||||
chr3:44394835
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.696-1565A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394835 | ||||||
chr3:44394836
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.696-1564G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394836 | ||||||
chr3:44394864
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG02818.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.696-1536G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394864 | ||||||
chr3:44394908
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0001g0200 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.696-1490_696-1470d others(23): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394908 | |||||
chr3:44394909
|
AAAAAAAA others(13): Show |
A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0138 | 3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.696-1489_696-1470d others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394909 | |||||
chr3:44394915
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0219 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.696-1483_696-1474d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394915 | |||||
chr3:44394915
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.696-1483_696-1470d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394915 | |||||
chr3:44394916
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0003g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.696-1482_696-1468d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394916 | |||||
chr3:44394917
|
AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0181 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.696-1481_696-1470d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394917 | |||||
chr3:44394917
|
AAAAAATA others(9): Show |
A | 2 | a0001c0001t0001g0145a0001c0001t0003g0052 | 2 | HG02040.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.696-1481_696-1466d others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394917 | |||||
chr3:44394918
|
AAAAATAT others(4): Show |
A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG00733.hp2 HG03471.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1480_696-1470d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | |||||
chr3:44394918
|
AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0007g0075 | 3 | HG03098.hp2 HG04199.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1468d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | |||||
chr3:44394918
|
AAAAATAT others(8): Show |
A | 3 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0007g0074 | 3 | HG01975.hp1 HG03041.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1466d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | |||||
chr3:44394918
|
AAAAATAT others(16): Show |
A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1458d others(25): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | |||||
chr3:44394918
|
AAAAATAT others(18): Show |
A | 2 | a0002c0002t0001g0028a0002c0002t0001g0081 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.696-1480_696-1456d others(27): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | |||||
chr3:44394919
|
AAAATATA others(1): Show |
A | 5 | a0001c0001t0001g0096a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-1479_696-1472d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | |||||
chr3:44394919
|
AAAATATA others(3): Show |
A | 2 | a0001c0001t0001g0131a0001c0001t0011g0233 | 2 | HG02965.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.696-1479_696-1470d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | |||||
chr3:44394919
|
AAAATATA others(5): Show |
A | 3 | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0180 | 3 | HG01891.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.696-1479_696-1468d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | |||||
chr3:44394919
|
AAAATATA others(7): Show |
A | 8 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0156others(5): Show | 9 | HG02523.hp2 HG02896.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1479_696-1466d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | |||||
chr3:44394920
|
AAATATAT others(2): Show |
A | 14 | a0001c0001t0001g0190a0001c0001t0001g0198a0001c0001t0001g0202others(11): Show | 14 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-1478_696-1470d others(11): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | |||||
chr3:44394920
|
AAATATAT others(4): Show |
A | 13 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0110others(10): Show | 13 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-1478_696-1468d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | |||||
chr3:44394920
|
AAATATAT others(6): Show |
A | 8 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0172others(5): Show | 8 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1478_696-1466d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | |||||
chr3:44394920
|
AAATATAT others(8): Show |
A | 6 | a0001c0001t0001g0155a0001c0001t0001g0179a0001c0001t0003g0061others(3): Show | 6 | HG02148.hp2 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1478_696-1464d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | |||||
chr3:44394920
|
AAATATAT others(16): Show |
A | 1 | a0002c0002t0001g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.696-1478_696-1456d others(25): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | |||||
chr3:44394921
|
A | T | 4 | a0001c0001t0001g0129a0001c0001t0002g0016a0001c0001t0002g0019others(1): Show | 4 | HG01192.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-1479A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394921 | ||||||
chr3:44394921
|
AAT | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0002g0036others(3): Show | 6 | HG01515.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1442_696-1441d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(1): Show |
A | 11 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0189others(8): Show | 11 | HG00597.hp1 HG00735.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-1448_696-1441d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(3): Show |
A | 8 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0101others(5): Show | 8 | HG01167.hp2 HG02683.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1450_696-1441d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(5): Show |
A | 6 | a0001c0001t0001g0111a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG02486.hp1 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1452_696-1441d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(7): Show |
A | 27 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0157others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.696-1454_696-1441d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.696-1458_696-1441d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394921
|
AATATATA others(17): Show |
A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696-1464_696-1441d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | |||||
chr3:44394922
|
AT | A | 3 | a0001c0001t0002g0035a0001c0001t0002g0042a0001c0001t0002g0079 | 3 | HG01346.hp1 HG01361.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1477delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATAT | A | 6 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0004g0086others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1477_696-1475d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATATATAT | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0204a0001c0001t0001g0214others(2): Show | 5 | HG02004.hp1 HG02572.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-1477_696-1471d others(9): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATATATAT others(2): Show |
A | 23 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0001g0122others(20): Show | 23 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.696-1477_696-1469d others(11): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATATATAT others(4): Show |
A | 10 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0112others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-1477_696-1467d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATATATAT others(6): Show |
A | 9 | a0001c0001t0001g0143a0001c0001t0001g0151a0001c0001t0003g0047others(6): Show | 9 | HG00673.hp2 HG01106.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1477_696-1465d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394922
|
ATATATAT others(8): Show |
A | 7 | a0001c0001t0001g0166a0001c0001t0003g0049a0001c0001t0003g0071others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-1477_696-1463d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | ||||||
chr3:44394923
|
T | A | 5 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0024others(2): Show | 5 | HG01243.hp2 HG01952.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-1477T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394923 | ||||||
chr3:44394925
|
T | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0018a0001c0001t0002g0032others(5): Show | 8 | HG01515.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1475T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394925 | ||||||
chr3:44394927
|
T | A | 12 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0040others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.696-1473T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394927 | ||||||
chr3:44394929
|
T | A | 3 | a0001c0001t0001g0209a0001c0001t0002g0011a0001c0001t0002g0044 | 3 | HG02572.hp2 HG02886.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.696-1471T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394929 | ||||||
chr3:44394931
|
T | A | 8 | a0001c0001t0001g0102a0001c0001t0001g0185a0001c0001t0001g0205others(5): Show | 8 | HG00597.hp1 HG02004.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1469T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394931 | ||||||
chr3:44394933
|
T | A | 16 | a0001c0001t0001g0095a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.696-1467T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394933 | ||||||
chr3:44394935
|
T | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0137a0001c0001t0001g0163others(5): Show | 8 | HG00438.hp1 HG00735.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1465T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394935 | ||||||
chr3:44394936
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.696-1456_696-1433d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394936 | |||||
chr3:44394937
|
T | A | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG00597.hp2 HG01106.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-1463T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394937 | ||||||
chr3:44394939
|
T | A | 9 | a0001c0001t0003g0048a0001c0001t0003g0073a0001c0001t0005g0003others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-1461T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394939 | ||||||
chr3:44394941
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.696-1459T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394941 | ||||||
chr3:44394948
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696-1452A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394948 | ||||||
chr3:44394958
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.696-1442A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394958 | ||||||
chr3:44395021
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.696-1379C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395021 | ||||||
chr3:44395396
|
A | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.696-1004A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395396 | ||||||
chr3:44395445
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.696-955A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395445 | ||||||
chr3:44395592
|
G | T | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.696-808G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395592 | ||||||
chr3:44395673
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.696-727T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395673 | ||||||
chr3:44395756
|
G | A | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.696-644G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395756 | ||||||
chr3:44395892
|
T | C | 4 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-508T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395892 | ||||||
chr3:44395935
|
C | T | 59 | a0001c0001t0001g0094a0001c0001t0001g0189a0001c0001t0001g0190others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.696-465C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395935 | ||||||
chr3:44395945
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-455C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395945 | ||||||
chr3:44395965
|
C | T | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049 | 3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.696-435C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395965 | ||||||
chr3:44396178
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.696-222A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396178 | ||||||
chr3:44396220
|
C | T | 4 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0058others(1): Show | 4 | HG00423.hp2 HG02040.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-180C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396220 | ||||||
chr3:44396289
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0145others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.696-111G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396289 | ||||||
chr3:44396378
|
A | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.696-22A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396378 | ||||||
chr3:44396569
|
C | CCAAATAA others(31): Show |
1 | a0001c0001t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793+109_793+110ins others(38): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 44396569 | |||||
chr3:44396627
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.794-116T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | chr3 | 44396627 | ||||||
chr3:44396631
|
A | C | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-112A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | chr3 | 44396631 | ||||||
chr3:44396873
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.885+39C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44396873 | ||||||
chr3:44397002
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.885+168A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397002 | ||||||
chr3:44397356
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.885+522T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397356 | ||||||
chr3:44397396
|
A | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.885+562A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397396 | ||||||
chr3:44397421
|
C | G | 34 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(31): Show | 34 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.885+587C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397421 | ||||||
chr3:44397576
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.885+742A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397576 | ||||||
chr3:44397675
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.885+841G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397675 | ||||||
chr3:44397752
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.885+918A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397752 | ||||||
chr3:44397856
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.885+1022C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397856 | ||||||
chr3:44397857
|
G | A | 2 | a0001c0001t0010g0068a0001c0001t0010g0076 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.885+1023G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397857 | ||||||
chr3:44397909
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.885+1075T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397909 | ||||||
chr3:44398056
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.885+1222C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398056 | ||||||
chr3:44398066
|
C | A | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.885+1232C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398066 | ||||||
chr3:44398249
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.885+1415C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398249 | ||||||
chr3:44398250
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0009g0063a0001c0001t0009g0064 | 3 | HG01257.hp2 HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.885+1416G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398250 | ||||||
chr3:44398279
|
A | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.885+1445A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398279 | ||||||
chr3:44398355
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.885+1521G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398355 | ||||||
chr3:44398360
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.885+1526A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398360 | ||||||
chr3:44398420
|
ACT | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.885+1587_885+1588d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398420 | ||||||
chr3:44398445
|
T | TTAGA | 28 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0102others(25): Show | 29 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.885+1662_885+1665d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398445
|
T | TTAGATAG others(1): Show |
9 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0149others(6): Show | 9 | HG01975.hp1 HG02615.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1658_885+1665d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398445
|
T | TTAGATAG others(5): Show |
5 | a0001c0001t0001g0129a0001c0001t0001g0140a0001c0001t0003g0054others(2): Show | 5 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+1654_885+1665d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398445
|
TTAGA | T | 54 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0108others(51): Show | 54 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.885+1662_885+1665d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398445
|
TTAGATAG others(1): Show |
T | 47 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0115others(44): Show | 48 | HG00140.hp1 HG00423.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.885+1658_885+1665d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398445
|
TTAGATAG others(5): Show |
T | 13 | a0001c0001t0001g0182a0001c0001t0001g0204a0001c0001t0001g0211others(10): Show | 13 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.885+1654_885+1665d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | |||||
chr3:44398511
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.885+1677C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398511 | ||||||
chr3:44398679
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.886-1676A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398679 | ||||||
chr3:44398697
|
C | A | 1 | a0001c0001t0020g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.886-1658C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398697 | ||||||
chr3:44399010
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886-1345G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399010 | ||||||
chr3:44399071
|
T | G | 1 | a0001c0001t0019g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.886-1284T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399071 | ||||||
chr3:44399386
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.886-969G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399386 | ||||||
chr3:44399808
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.886-547G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399808 | ||||||
chr3:44399903
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.886-452C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399903 | ||||||
chr3:44400840
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1118+253A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44400840 | ||||||
chr3:44400868
|
T | A | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1118+281T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44400868 | ||||||
chr3:44401179
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1119-24C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44401179 | ||||||
chr3:44401735
|
C | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+401C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44401735 | ||||||
chr3:44402037
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1250+703T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402037 | ||||||
chr3:44402074
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1250+740T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402074 | ||||||
chr3:44402284
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+950G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402284 | ||||||
chr3:44402420
|
ATG | A | 35 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0049others(32): Show | 35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1250+1088_1250+108 others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44402420 | |||||
chr3:44402610
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1250+1276C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402610 | ||||||
chr3:44402831
|
G | A | 5 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+1497G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402831 | ||||||
chr3:44403162
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1250+1828G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403162 | ||||||
chr3:44403162
|
G | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0146others(33): Show | 37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1250+1828G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403162 | ||||||
chr3:44403255
|
C | T | 9 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+1921C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403255 | ||||||
chr3:44403415
|
C | G | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+2081C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403415 | ||||||
chr3:44403580
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1250+2246G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403580 | ||||||
chr3:44403641
|
G | T | 1 | a0001c0001t0003g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1250+2307G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403641 | ||||||
chr3:44403717
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1250+2383G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403717 | ||||||
chr3:44403849
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1250+2515C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403849 | ||||||
chr3:44403860
|
GATGGCCT others(3): Show |
G | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1250+2527_1250+253 others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403860 | ||||||
chr3:44404011
|
C | G | 4 | a0001c0003t0001g0014a0001c0003t0001g0026a0001c0003t0001g0085others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+2677C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404011 | ||||||
chr3:44404368
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+3034C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404368 | ||||||
chr3:44404736
|
T | C | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-2706T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404736 | ||||||
chr3:44404808
|
AT | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 46 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1251-2627delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44404808 | |||||
chr3:44405109
|
C | CCAGCCTG others(10): Show |
1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2332_1251-233 others(21): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405109 | |||||
chr3:44405117
|
C | G | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2325C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405117 | ||||||
chr3:44405122
|
G | T | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2320G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405122 | ||||||
chr3:44405131
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2311G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405131 | ||||||
chr3:44405132
|
A | G | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2310A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405132 | ||||||
chr3:44405143
|
C | A | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2299C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405143 | ||||||
chr3:44405151
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2291T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405151 | ||||||
chr3:44405163
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1251-2279G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405163 | ||||||
chr3:44405198
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-2244C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405198 | ||||||
chr3:44405345
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0088others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-2097G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405345 | ||||||
chr3:44405570
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-1872A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405570 | ||||||
chr3:44405605
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-1837C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405605 | ||||||
chr3:44405844
|
TG | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1251-1595delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405844 | |||||
chr3:44405909
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0177 | 2 | NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1251-1533G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405909 | ||||||
chr3:44405951
|
C | CA | 41 | a0001c0001t0002g0035a0001c0001t0002g0046a0001c0001t0002g0079others(38): Show | 41 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1251-1470dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405951 | |||||
chr3:44405951
|
CA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(161): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1251-1470delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405951 | |||||
chr3:44406044
|
G | T | 1 | a0001c0001t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-1398G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406044 | ||||||
chr3:44406392
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1251-1050C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406392 | ||||||
chr3:44406482
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-960T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406482 | ||||||
chr3:44406483
|
A | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-959A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406483 | ||||||
chr3:44406484
|
T | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-958T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406484 | ||||||
chr3:44406486
|
C | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-956C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406486 | ||||||
chr3:44406489
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-953A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406489 | ||||||
chr3:44406490
|
GTA | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-951_1251-950d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406490 | ||||||
chr3:44406493
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(212): Show | 217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1251-949A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406493 | ||||||
chr3:44406599
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1251-843T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406599 | ||||||
chr3:44406623
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1251-819T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406623 | ||||||
chr3:44406628
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-814G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406628 | ||||||
chr3:44406810
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0240 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1251-632C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406810 | ||||||
chr3:44407161
|
T | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0172 | 2 | HG02683.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1251-281T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44407161 |