geneid | 10043 |
---|---|
ensemblid | ENSG00000100284.22 |
hgncid | 11982 |
symbol | TOM1 |
name | target of myb1 membrane trafficking protein |
refseq_nuc | NM_005488.3 |
refseq_prot | NP_005479.1 |
ensembl_nuc | ENST00000449058.7 |
ensembl_prot | ENSP00000394466.2 |
mane_status | MANE Select |
chr | chr22 |
start | 35299894 |
end | 35347973 |
strand | + |
ver | v1.2 |
region | chr22:35299894-35347973 |
region5000 | chr22:35294894-35352973 |
regionname0 | TOM1_chr22_35299894_35347973 |
regionname5000 | TOM1_chr22_35294894_35352973 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 492 | 353 | 84 | 68 | 156 | 10 | 33 | 116 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0002 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0003 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0004 | 0/0 | 492 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0005 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0006 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1479 | 229 | 24 | 46 | 128 | 6 | 24 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0002 | 0/1 | 1479 | 111 | 52 | 20 | 25 | 4 | 9 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0003 | 0/0 | 1479 | 6 | 4 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0004 | 0/0 | 1479 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0005 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0006 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0007 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0008 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0009 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0010 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0011 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0012 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0013 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
c0014 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 800 | 348 | 79 | 70 | 153 | 10 | 34 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
t0002 | 0/0 | 800 | 7 | 5 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
t0003 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
t0004 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
t0005 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0003 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0291 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1479 | 229 | 24 | 46 | 128 | 6 | 24 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0002 | 0/1 | 1479 | 111 | 52 | 20 | 25 | 4 | 9 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0003 | 0/0 | 1479 | 6 | 4 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0004 | 0/0 | 1479 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0006 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0007 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0010 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0013 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0014 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0002c0005 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0003c0009 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0004c0011 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0005c0012 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0006c0008 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2278 | 225 | 22 | 46 | 126 | 6 | 24 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0001t0002 | 0/0 | 2278 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0001t0004 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0001t0005 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0002t0001 | 0/1 | 2278 | 108 | 51 | 18 | 25 | 4 | 9 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0002t0002 | 0/0 | 2278 | 3 | 1 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0003t0001 | 0/0 | 2278 | 3 | 2 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0003t0002 | 0/0 | 2278 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0003t0003 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0004t0001 | 0/0 | 2278 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0006t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0007t0001 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0010t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0013t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0001c0014t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0002c0005t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0003c0009t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0004c0011t0001 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0005c0012t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
a0006c0008t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | copy fasta | chr22 | 35294894 | 35352973 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0291 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0010t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0013t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0001c0014t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0002c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0003c0009t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0004c0011t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0005c0012t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
a0006c0008t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0061 | EUR | GBR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0087 | EUR | FIN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0298 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01081 | hp2 | a0003 | c0009 | t0001 | g0104 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0245 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01255 | hp2 | a0001 | c0010 | t0001 | g0219 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01261 | hp1 | a0002 | c0005 | t0001 | g0080 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01496 | hp2 | a0005 | c0012 | t0001 | g0229 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0062 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01978 | hp1 | a0006 | c0008 | t0001 | g0163 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02055 | hp2 | a0001 | c0014 | t0001 | g0309 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0300 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0301 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0307 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0189 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04228 | hp1 | a0004 | c0011 | t0001 | g0188 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18943 | hp2 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18969 | hp2 | a0001 | c0007 | t0001 | g0165 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19063 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19240 | hp1 | a0001 | c0013 | t0001 | g0308 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ASW | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ASW | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0215 | EUR | TSI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | USA | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | USA | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0123 | REF | REF | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0291 | REF | REF | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35330471
|
G | A | 1 | a0002 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.890G>A | p.Arg297His | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/15 | 925/2278 | 890/1479 | 297/492 | chr22 | 35330471 | ||
chr22:35338744
|
G | A | 1 | a0006 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1180G>A | p.Gly394Ser | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/15 | 1215/2278 | 1180/1479 | 394/492 | chr22 | 35338744 | ||
chr22:35346940
|
C | T | 1 | a0005 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1295C>T | p.Ala432Val | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 14/15 | 1330/2278 | 1295/1479 | 432/492 | chr22 | 35346940 | ||
chr22:35347097
|
G | A | 1 | a0003 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1367G>A | p.Arg456Gln | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1402/2278 | 1367/1479 | 456/492 | chr22 | 35347097 | ||
chr22:35347136
|
C | T | 1 | a0004 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1406C>T | p.Pro469Leu | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1441/2278 | 1406/1479 | 469/492 | chr22 | 35347136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35317938
|
C | T | 2 | a0001c0013a0001c0014 | 2 | HG02055.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.114C>T | p.Asp38Asp | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/15 | 149/2278 | 114/1479 | 38/492 | chr22 | 35317938 | ||
chr22:35327327
|
G | A | 1 | a0001c0004 | 2 | HG01099.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.705G>A | p.Ser235Ser | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/15 | 740/2278 | 705/1479 | 235/492 | chr22 | 35327327 | ||
chr22:35333424
|
G | A | 1 | a0001c0006 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.954G>A | p.Pro318Pro | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/15 | 989/2278 | 954/1479 | 318/492 | chr22 | 35333424 | ||
chr22:35334410
|
G | A | 1 | a0001c0007 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.1110G>A | p.Ala370Ala | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/15 | 1145/2278 | 1110/1479 | 370/492 | chr22 | 35334410 | ||
chr22:35346932
|
T | G | 5 | a0001c0002a0001c0003a0001c0013others(2): Show | 120 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
splice_region_variant&synonymous_variant | LOW | c.1287T>G | p.Gly429Gly | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 14/15 | 1322/2278 | 1287/1479 | 429/492 | chr22 | 35346932 | ||
chr22:35347131
|
G | C | 3 | a0001c0002a0001c0013a0006c0008 | 113 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(110): Show |
synonymous_variant | LOW | c.1401G>C | p.Gly467Gly | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1436/2278 | 1401/1479 | 467/492 | chr22 | 35347131 | ||
chr22:35347185
|
T | C | 1 | a0001c0010 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1455T>C | p.Asp485Asp | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1490/2278 | 1455/1479 | 485/492 | chr22 | 35347185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35299901
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0003t0002 | 7 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/15 | 28 | chr22 | 35299901 | |||||
chr22:35347210
|
G | C | 1 | a0001c0003t0003 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1 | chr22 | 35347210 | |||||
chr22:35347342
|
C | T | 1 | a0001c0001t0005 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 133 | chr22 | 35347342 | |||||
chr22:35347886
|
G | T | 1 | a0001c0001t0004 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 677 | chr22 | 35347886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35300021
|
C | G | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+41C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300021 | ||||||
chr22:35300084
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(22): Show | 29 | HG01168.hp1 HG01169.hp2 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.52+104G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300084 | ||||||
chr22:35300084
|
G | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+104G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300084 | ||||||
chr22:35300099
|
G | T | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.52+119G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300099 | ||||||
chr22:35300148
|
G | A | 1 | a0001c0002t0001g0170 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.52+168G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300148 | ||||||
chr22:35300287
|
G | T | 1 | a0001c0002t0001g0306 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.52+307G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300287 | ||||||
chr22:35300322
|
G | A | 4 | a0001c0001t0001g0171a0001c0002t0001g0009a0001c0002t0001g0172others(1): Show | 6 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+342G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300322 | ||||||
chr22:35300511
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+531G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300511 | ||||||
chr22:35300515
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0305 | 6 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+535C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300515 | ||||||
chr22:35300737
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.52+757A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300737 | ||||||
chr22:35300905
|
AC | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+926delC | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300905 | ||||||
chr22:35300938
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(165): Show | 191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.52+958A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300938 | ||||||
chr22:35301048
|
C | CA | 55 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0031others(52): Show | 59 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.52+1089dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | |||||
chr22:35301048
|
CA | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0295a0001c0002t0001g0005others(2): Show | 7 | HG00099.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1089delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | |||||
chr22:35301048
|
CAAAAA | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 145 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.52+1085_52+1089del others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | |||||
chr22:35301267
|
T | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.52+1287T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301267 | ||||||
chr22:35301273
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.52+1293A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301273 | ||||||
chr22:35301312
|
ATATATAT | A | 4 | a0001c0001t0001g0052a0001c0002t0001g0005a0001c0002t0001g0050others(1): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+1338_52+1344del others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301312 | |||||
chr22:35301314
|
ATATAT | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+1340_52+1344del others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301314 | |||||
chr22:35301370
|
A | G | 9 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0002t0001g0302others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1390A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301370 | ||||||
chr22:35301399
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+1419A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301399 | ||||||
chr22:35301523
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.52+1543T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301523 | ||||||
chr22:35301527
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.52+1547C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301527 | ||||||
chr22:35301619
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.52+1639G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301619 | ||||||
chr22:35301697
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+1717C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301697 | ||||||
chr22:35301702
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.52+1722T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301702 | ||||||
chr22:35301811
|
C | CT | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+1831_52+1832ins others(1): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301811 | ||||||
chr22:35301978
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+1998C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301978 | ||||||
chr22:35302037
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+2057A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302037 | ||||||
chr22:35302056
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+2076C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302056 | ||||||
chr22:35302069
|
G | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2089G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302069 | ||||||
chr22:35302074
|
G | A | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.52+2094G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302074 | ||||||
chr22:35302255
|
A | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2275A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302255 | ||||||
chr22:35302306
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+2326T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302306 | ||||||
chr22:35302330
|
CT | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.52+2372delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | |||||
chr22:35302330
|
CTT | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0034others(23): Show | 30 | HG01257.hp2 HG02027.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.52+2371_52+2372del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | |||||
chr22:35302330
|
CTTT | C | 16 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0002g0297others(13): Show | 18 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+2370_52+2372del others(3): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | |||||
chr22:35302330
|
CTTTT | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0037others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+2369_52+2372del others(4): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | |||||
chr22:35302336
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.52+2356T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302336 | ||||||
chr22:35302337
|
T | C | 3 | a0001c0002t0001g0002a0001c0002t0001g0212a0001c0002t0001g0305 | 7 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+2357T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302337 | ||||||
chr22:35302358
|
T | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+2378T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302358 | ||||||
chr22:35302422
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.52+2442G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302422 | ||||||
chr22:35302462
|
AG | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.52+2484delG | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302462 | |||||
chr22:35302484
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.52+2504G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302484 | ||||||
chr22:35302489
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.52+2509G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302489 | ||||||
chr22:35302498
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+2518G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302498 | ||||||
chr22:35302600
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+2620G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302600 | ||||||
chr22:35302620
|
C | T | 2 | a0001c0002t0001g0154a0001c0002t0001g0155 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.52+2640C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302620 | ||||||
chr22:35302697
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.52+2717T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302697 | ||||||
chr22:35302896
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+2916C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302896 | ||||||
chr22:35302993
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.52+3013C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302993 | ||||||
chr22:35303052
|
A | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3072A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303052 | ||||||
chr22:35303110
|
T | G | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | HG00099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.52+3130T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303110 | ||||||
chr22:35303111
|
T | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+3131T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303111 | ||||||
chr22:35303131
|
A | AACACACA others(3): Show |
141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(138): Show | 164 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.52+3160_52+3169dup others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | |||||
chr22:35303131
|
A | AACACACA others(5): Show |
6 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0064others(3): Show | 6 | HG02735.hp1 HG03017.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+3158_52+3169dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | |||||
chr22:35303131
|
A | AACACACA others(11): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+3152_52+3169dup others(18): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | |||||
chr22:35303202
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.52+3222C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303202 | ||||||
chr22:35303272
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+3292C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303272 | ||||||
chr22:35303379
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.52+3399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303379 | ||||||
chr22:35303460
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3480A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303460 | ||||||
chr22:35303504
|
C | CT | 14 | a0001c0001t0001g0036a0001c0001t0001g0149a0001c0001t0001g0150others(11): Show | 14 | HG01175.hp1 HG02135.hp2 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.52+3542dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303504 | |||||
chr22:35303504
|
CT | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0177others(5): Show | 8 | HG01069.hp1 HG01123.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+3542delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303504 | |||||
chr22:35303589
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3609C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303589 | ||||||
chr22:35303620
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3640C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303620 | ||||||
chr22:35303670
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3690G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303670 | ||||||
chr22:35303766
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3786G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303766 | ||||||
chr22:35303772
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3792G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303772 | ||||||
chr22:35303823
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3843A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303823 | ||||||
chr22:35303826
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3846C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303826 | ||||||
chr22:35303831
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0176others(25): Show | 32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.52+3851A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303831 | ||||||
chr22:35303864
|
T | C | 2 | a0001c0001t0001g0069a0001c0002t0001g0070 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.52+3884T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303864 | ||||||
chr22:35303890
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+3910C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303890 | ||||||
chr22:35303937
|
T | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+3957T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303937 | ||||||
chr22:35303990
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 13 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+4010C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303990 | ||||||
chr22:35304183
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 8 | HG00438.hp2 HG02056.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+4203C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304183 | ||||||
chr22:35304262
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4282A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304262 | ||||||
chr22:35304419
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.52+4439G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304419 | ||||||
chr22:35304474
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4494G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304474 | ||||||
chr22:35304495
|
A | C | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.52+4515A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304495 | ||||||
chr22:35304495
|
A | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.52+4515A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304495 | ||||||
chr22:35304526
|
G | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4546G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304526 | ||||||
chr22:35304624
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(195): Show | 225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.52+4644A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304624 | ||||||
chr22:35304730
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.52+4750G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304730 | ||||||
chr22:35304770
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4790A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304770 | ||||||
chr22:35304774
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4794G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304774 | ||||||
chr22:35304811
|
A | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+4831A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304811 | ||||||
chr22:35305170
|
C | T | 1 | a0001c0002t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.52+5190C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305170 | ||||||
chr22:35305230
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5250G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305230 | ||||||
chr22:35305261
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5281G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305261 | ||||||
chr22:35305433
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5453G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305433 | ||||||
chr22:35305457
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(292): Show | 342 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.52+5477T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305457 | ||||||
chr22:35305464
|
A | G | 32 | a0001c0001t0001g0012a0001c0001t0001g0171a0001c0001t0001g0191others(29): Show | 36 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+5484A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305464 | ||||||
chr22:35305580
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5600A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305580 | ||||||
chr22:35305616
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5636C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305616 | ||||||
chr22:35305658
|
CAA | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5693_52+5694del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35305658 | |||||
chr22:35305729
|
T | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5749T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305729 | ||||||
chr22:35305730
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5750G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305730 | ||||||
chr22:35305859
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0142others(1): Show | 6 | HG02293.hp2 NA18974.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+5879C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305859 | ||||||
chr22:35305860
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+5880G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305860 | ||||||
chr22:35305905
|
A | AGAGTG | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+5927_52+5928ins others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35305905 | |||||
chr22:35305967
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.52+5987C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305967 | ||||||
chr22:35306057
|
G | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030 | 3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.52+6077G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306057 | ||||||
chr22:35306075
|
A | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(196): Show | 226 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.52+6095A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306075 | ||||||
chr22:35306088
|
A | G | 1 | a0001c0002t0001g0306 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.52+6108A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306088 | ||||||
chr22:35306144
|
CT | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.52+6174delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35306144 | |||||
chr22:35306154
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.52+6174T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306154 | ||||||
chr22:35306181
|
A | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+6201A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306181 | ||||||
chr22:35306303
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+6323G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306303 | ||||||
chr22:35306379
|
T | G | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+6399T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306379 | ||||||
chr22:35306446
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+6466G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306446 | ||||||
chr22:35306711
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.52+6731G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306711 | ||||||
chr22:35306748
|
A | AC | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+6771dupC | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35306748 | |||||
chr22:35306958
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.52+6978T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306958 | ||||||
chr22:35307041
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+7061A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307041 | ||||||
chr22:35307135
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.52+7155T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307135 | ||||||
chr22:35307235
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+7255T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307235 | ||||||
chr22:35307288
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+7308A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307288 | ||||||
chr22:35307323
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+7343G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307323 | ||||||
chr22:35307329
|
T | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+7349T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307329 | ||||||
chr22:35307373
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+7393T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307373 | ||||||
chr22:35307462
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0141a0001c0001t0001g0284others(1): Show | 5 | HG00099.hp1 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+7482G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307462 | ||||||
chr22:35307464
|
A | T | 1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.52+7484A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307464 | ||||||
chr22:35307558
|
T | A | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 332 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.52+7578T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307558 | ||||||
chr22:35307661
|
T | C | 8 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0002t0002g0296others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+7681T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307661 | ||||||
chr22:35308087
|
C | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG00733.hp1 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+8107C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308087 | ||||||
chr22:35308155
|
T | C | 1 | a0001c0010t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.52+8175T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308155 | ||||||
chr22:35308189
|
A | G | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+8209A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308189 | ||||||
chr22:35308199
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0050a0001c0002t0001g0051 | 5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+8219C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308199 | ||||||
chr22:35308217
|
T | C | 3 | a0001c0002t0001g0002a0001c0002t0001g0212a0001c0002t0001g0305 | 7 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+8237T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308217 | ||||||
chr22:35308228
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.52+8248G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308228 | ||||||
chr22:35308275
|
CT | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.52+8310delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308275 | |||||
chr22:35308290
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+8310T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308290 | ||||||
chr22:35308291
|
C | CT | 23 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0039others(20): Show | 25 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+8321dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308291 | |||||
chr22:35308291
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+8311C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308291 | ||||||
chr22:35308355
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+8375C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308355 | ||||||
chr22:35308421
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.52+8441C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308421 | ||||||
chr22:35308441
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0176others(24): Show | 31 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.52+8461A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308441 | ||||||
chr22:35308602
|
TCCCTGAC others(5): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.52+8624_52+8635del others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308602 | |||||
chr22:35308619
|
G | C | 179 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(176): Show | 209 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.52+8639G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308619 | ||||||
chr22:35308654
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.52+8674A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308654 | ||||||
chr22:35309239
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-8638G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309239 | ||||||
chr22:35309366
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.53-8511A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309366 | ||||||
chr22:35309476
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.53-8401T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309476 | ||||||
chr22:35309523
|
A | G | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.53-8354A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309523 | ||||||
chr22:35309568
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.53-8309G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309568 | ||||||
chr22:35309636
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.53-8241T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309636 | ||||||
chr22:35309643
|
C | CA | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-8217dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35309643 | |||||
chr22:35309643
|
CA | C | 6 | a0001c0001t0001g0216a0001c0001t0001g0271a0001c0002t0001g0236others(3): Show | 6 | HG02723.hp2 HG02735.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-8217delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35309643 | |||||
chr22:35309659
|
A | G | 8 | a0001c0001t0001g0216a0001c0001t0001g0238a0001c0002t0001g0026others(5): Show | 10 | HG00544.hp1 NA18939.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.53-8218A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309659 | ||||||
chr22:35309738
|
A | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0002t0001g0180 | 3 | HG02257.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53-8139A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309738 | ||||||
chr22:35309875
|
C | A | 1 | a0001c0002t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-8002C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309875 | ||||||
chr22:35309878
|
G | C | 1 | a0001c0002t0001g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53-7999G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309878 | ||||||
chr22:35309949
|
G | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-7928G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309949 | ||||||
chr22:35310040
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0137 | 3 | HG03704.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.53-7837C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310040 | ||||||
chr22:35310261
|
T | TTAAAAGT others(311): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-7604_53-7603ins others(318): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35310261 | |||||
chr22:35310537
|
G | C | 1 | a0001c0002t0001g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.53-7340G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310537 | ||||||
chr22:35310577
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0252a0001c0001t0001g0259others(12): Show | 17 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-7300G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310577 | ||||||
chr22:35310586
|
A | G | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-7291A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310586 | ||||||
chr22:35310670
|
A | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-7207A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310670 | ||||||
chr22:35310727
|
G | GGTACTGC others(5): Show |
1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.53-7149_53-7138dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35310727 | |||||
chr22:35310743
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-7134C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310743 | ||||||
chr22:35310959
|
G | A | 4 | a0001c0001t0001g0052a0001c0002t0001g0005a0001c0002t0001g0050others(1): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-6918G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310959 | ||||||
chr22:35311243
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 207 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.53-6634G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311243 | ||||||
chr22:35311258
|
C | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-6619C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311258 | ||||||
chr22:35311280
|
G | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-6597G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311280 | ||||||
chr22:35311335
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-6542A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311335 | ||||||
chr22:35311358
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.53-6519C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311358 | ||||||
chr22:35311424
|
G | A | 6 | a0001c0001t0001g0187a0001c0001t0001g0277a0001c0002t0001g0186others(3): Show | 6 | HG01123.hp2 HG01358.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-6453G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311424 | ||||||
chr22:35311430
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53-6447T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311430 | ||||||
chr22:35311431
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53-6446C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311431 | ||||||
chr22:35311510
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.53-6367G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311510 | ||||||
chr22:35311595
|
C | T | 10 | a0001c0001t0001g0187a0001c0001t0001g0277a0001c0002t0001g0186others(7): Show | 10 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-6282C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311595 | ||||||
chr22:35311604
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-6273G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311604 | ||||||
chr22:35311841
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.53-6036A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311841 | ||||||
chr22:35311869
|
G | A | 1 | a0001c0002t0001g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.53-6008G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311869 | ||||||
chr22:35312176
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-5701G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312176 | ||||||
chr22:35312243
|
CA | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(23): Show | 28 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.53-5618delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35312243 | |||||
chr22:35312243
|
CAA | C | 116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 139 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.53-5619_53-5618del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35312243 | |||||
chr22:35312369
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.53-5508G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312369 | ||||||
chr22:35312438
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-5439C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312438 | ||||||
chr22:35312529
|
G | A | 4 | a0001c0001t0001g0052a0001c0002t0001g0005a0001c0002t0001g0050others(1): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5348G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312529 | ||||||
chr22:35312576
|
A | G | 10 | a0001c0001t0001g0133a0001c0002t0001g0061a0001c0002t0001g0062others(7): Show | 10 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-5301A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312576 | ||||||
chr22:35312797
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.53-5080C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312797 | ||||||
chr22:35312806
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-5071G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312806 | ||||||
chr22:35312815
|
A | G | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-5062A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312815 | ||||||
chr22:35312828
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-5049T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312828 | ||||||
chr22:35312843
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.53-5034C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312843 | ||||||
chr22:35313072
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-4805G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313072 | ||||||
chr22:35313117
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-4760C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313117 | ||||||
chr22:35313144
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG00438.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.53-4733C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313144 | ||||||
chr22:35313228
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.53-4649T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313228 | ||||||
chr22:35313240
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-4637G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313240 | ||||||
chr22:35313261
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-4616C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313261 | ||||||
chr22:35313313
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.53-4564C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313313 | ||||||
chr22:35313344
|
C | CA | 5 | a0001c0001t0001g0052a0001c0001t0001g0088a0001c0002t0001g0005others(2): Show | 7 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-4521dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35313344 | |||||
chr22:35313416
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-4461G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313416 | ||||||
chr22:35313551
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.53-4326A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313551 | ||||||
chr22:35313772
|
C | T | 10 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0002t0001g0302others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-4105C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313772 | ||||||
chr22:35313867
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-4010C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313867 | ||||||
chr22:35313908
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3969G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313908 | ||||||
chr22:35314141
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.53-3736A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314141 | ||||||
chr22:35314180
|
G | A | 3 | a0001c0002t0001g0213a0001c0002t0001g0224a0001c0002t0001g0279 | 3 | NA18977.hp2 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.53-3697G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314180 | ||||||
chr22:35314217
|
A | ATG | 132 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.53-3658_53-3657dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314217 | |||||
chr22:35314224
|
A | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0154a0001c0002t0001g0155 | 4 | HG01070.hp1 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-3653A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314224 | ||||||
chr22:35314238
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 29 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.53-3639G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314238 | ||||||
chr22:35314324
|
C | T | 10 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0002t0001g0302others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3553C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314324 | ||||||
chr22:35314363
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044 | 5 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-3514A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314363 | ||||||
chr22:35314456
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.53-3421C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314456 | ||||||
chr22:35314456
|
CG | C | 15 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0041others(12): Show | 16 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.53-3415delG | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314456 | |||||
chr22:35314712
|
C | T | 2 | a0001c0003t0002g0300a0001c0003t0002g0301 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.53-3165C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314712 | ||||||
chr22:35314879
|
C | CTCATGAG others(1): Show |
10 | a0001c0001t0001g0038a0001c0001t0001g0220a0001c0001t0001g0294others(7): Show | 11 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-2996_53-2989dup others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314879 | |||||
chr22:35315097
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-2780C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315097 | ||||||
chr22:35315105
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.53-2772A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315105 | ||||||
chr22:35315196
|
A | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0002g0299others(4): Show | 9 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-2681A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315196 | ||||||
chr22:35315260
|
G | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 9 | HG02027.hp2 HG02132.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-2617G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315260 | ||||||
chr22:35315328
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.53-2549G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315328 | ||||||
chr22:35315393
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.53-2484G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315393 | ||||||
chr22:35315451
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53-2426C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315451 | ||||||
chr22:35315452
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53-2425C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315452 | ||||||
chr22:35315550
|
A | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(23): Show | 29 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.53-2327A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315550 | ||||||
chr22:35315718
|
C | A | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53-2159C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315718 | ||||||
chr22:35315820
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-2057G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315820 | ||||||
chr22:35315895
|
A | G | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.53-1982A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315895 | ||||||
chr22:35315938
|
G | A | 1 | a0001c0002t0001g0224 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.53-1939G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315938 | ||||||
chr22:35315948
|
C | T | 2 | a0001c0002t0001g0190a0001c0002t0001g0215 | 2 | HG01106.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.53-1929C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315948 | ||||||
chr22:35315975
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0064 | 2 | HG03471.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.53-1902G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315975 | ||||||
chr22:35316139
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-1738C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316139 | ||||||
chr22:35316184
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-1693C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316184 | ||||||
chr22:35316498
|
T | C | 10 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0002t0001g0302others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1379T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316498 | ||||||
chr22:35316560
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.53-1317A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316560 | ||||||
chr22:35316585
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.53-1292G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316585 | ||||||
chr22:35316621
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-1256C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316621 | ||||||
chr22:35316622
|
G | A | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.53-1255G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316622 | ||||||
chr22:35316629
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-1248G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316629 | ||||||
chr22:35317000
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0187a0001c0002t0001g0186others(2): Show | 5 | HG01123.hp2 HG01358.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-877C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317000 | ||||||
chr22:35317091
|
G | A | 1 | a0001c0001t0005g0090 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.53-786G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317091 | ||||||
chr22:35317206
|
G | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0125others(2): Show | 7 | HG00597.hp2 NA18970.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-671G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317206 | ||||||
chr22:35317353
|
C | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.53-524C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317353 | ||||||
chr22:35317468
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-409G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317468 | ||||||
chr22:35317523
|
A | G | 3 | a0001c0002t0001g0213a0001c0002t0001g0224a0001c0002t0001g0279 | 3 | NA18977.hp2 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.53-354A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317523 | ||||||
chr22:35317581
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.53-296G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317581 | ||||||
chr22:35317839
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.53-38A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317839 | ||||||
chr22:35318011
|
C | T | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.137+50C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318011 | ||||||
chr22:35318052
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.137+91G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318052 | ||||||
chr22:35318214
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.137+253C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318214 | ||||||
chr22:35318318
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030 | 3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+357G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318318 | ||||||
chr22:35318466
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.137+505G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318466 | ||||||
chr22:35318645
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.137+684C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318645 | ||||||
chr22:35318657
|
G | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030 | 3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+696G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318657 | ||||||
chr22:35318747
|
G | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.137+786G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318747 | ||||||
chr22:35318760
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.137+799G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318760 | ||||||
chr22:35318986
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 14 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.137+1025T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318986 | ||||||
chr22:35319271
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.137+1310C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319271 | ||||||
chr22:35319275
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137+1314G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319275 | ||||||
chr22:35319392
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG00733.hp1 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1431G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319392 | ||||||
chr22:35319816
|
G | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0176others(24): Show | 31 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.137+1855G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319816 | ||||||
chr22:35319848
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.137+1887T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319848 | ||||||
chr22:35319857
|
G | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 24 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.137+1896G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319857 | ||||||
chr22:35319949
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0030 | 3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+1988G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319949 | ||||||
chr22:35319964
|
C | T | 11 | a0001c0001t0001g0171a0001c0002t0001g0009a0001c0002t0001g0172others(8): Show | 13 | HG01891.hp2 HG02717.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.138-1995C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319964 | ||||||
chr22:35320122
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.138-1837A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320122 | ||||||
chr22:35320269
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.138-1690A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320269 | ||||||
chr22:35320364
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.138-1595G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320364 | ||||||
chr22:35320497
|
G | A | 1 | a0001c0002t0001g0241 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.138-1462G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320497 | ||||||
chr22:35320601
|
G | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.138-1358G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320601 | ||||||
chr22:35320987
|
G | GA | 25 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(22): Show | 28 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.138-958dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(5): Show |
1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.138-969_138-958dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(6): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0122 | 2 | HG01099.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.138-970_138-958dup others(13): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(7): Show |
88 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 103 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.138-971_138-958dup others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(8): Show |
40 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0053others(37): Show | 44 | HG00438.hp2 HG01346.hp2 HG01433.hp1 others(41): Show |
intron_variant | MODIFIER | c.138-958_138-957ins others(15): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(9): Show |
1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.138-958_138-957ins others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35320987
|
G | GAAAAAAA others(10): Show |
1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.138-958_138-957ins others(17): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | |||||
chr22:35321000
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0125others(1): Show | 6 | HG00597.hp2 NA18971.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-958_138-957ins others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35321000 | |||||
chr22:35321222
|
G | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.138-737G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321222 | ||||||
chr22:35321253
|
T | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.138-706T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321253 | ||||||
chr22:35321382
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.138-577C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321382 | ||||||
chr22:35321406
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0148 | 4 | NA18981.hp1 NA18990.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-553T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321406 | ||||||
chr22:35321547
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(21): Show | 27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.138-412T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321547 | ||||||
chr22:35321601
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138-358G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321601 | ||||||
chr22:35321750
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.138-209C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321750 | ||||||
chr22:35321842
|
A | C | 8 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0208others(5): Show | 16 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-117A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321842 | ||||||
chr22:35321878
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138-81A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321878 | ||||||
chr22:35322108
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.216+71C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322108 | ||||||
chr22:35322247
|
G | A | 2 | a0001c0001t0001g0038a0001c0002t0001g0033 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.216+210G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322247 | ||||||
chr22:35322255
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.216+218C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322255 | ||||||
chr22:35322297
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 22 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.216+260C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322297 | ||||||
chr22:35322325
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.216+288C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322325 | ||||||
chr22:35322360
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+323G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322360 | ||||||
chr22:35322384
|
G | A | 2 | a0001c0001t0001g0052a0001c0002t0001g0033 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.216+347G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322384 | ||||||
chr22:35322437
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.216+400C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322437 | ||||||
chr22:35322798
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.217-230T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322798 | ||||||
chr22:35322823
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.217-205C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322823 | ||||||
chr22:35322941
|
G | A | 1 | a0001c0002t0001g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.217-87G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322941 | ||||||
chr22:35323290
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366+113C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323290 | ||||||
chr22:35323308
|
G | A | 17 | a0001c0001t0001g0216a0001c0001t0001g0238a0001c0002t0001g0024others(14): Show | 19 | HG00733.hp2 HG01074.hp1 HG02698.hp2 others(16): Show |
intron_variant | MODIFIER | c.366+131G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323308 | ||||||
chr22:35323313
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.366+136G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323313 | ||||||
chr22:35323385
|
T | TA | 36 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0031others(33): Show | 41 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.367-96dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr22 | 35323385 | |||||
chr22:35323641
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.501+11T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 5/14 | chr22 | 35323641 | ||||||
chr22:35323732
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.502-36C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 5/14 | chr22 | 35323732 | ||||||
chr22:35323961
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.648+47A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35323961 | ||||||
chr22:35324142
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.648+228T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324142 | ||||||
chr22:35324412
|
C | CA | 30 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(27): Show | 43 | HG00423.hp2 HG01884.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.648+522dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | |||||
chr22:35324412
|
C | CAA | 38 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0036others(35): Show | 42 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.648+521_648+522dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | |||||
chr22:35324412
|
C | CAAA | 6 | a0001c0001t0001g0031a0001c0001t0001g0259a0001c0002t0001g0192others(3): Show | 6 | HG02572.hp2 NA18522.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+520_648+522dup others(3): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | |||||
chr22:35324412
|
CA | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0066a0001c0001t0001g0081others(13): Show | 16 | HG00323.hp2 HG01069.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+522delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | |||||
chr22:35324412
|
CAA | C | 8 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(5): Show | 8 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.648+521_648+522del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | |||||
chr22:35324950
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.648+1036G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324950 | ||||||
chr22:35324955
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.648+1041G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324955 | ||||||
chr22:35324996
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.648+1082C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324996 | ||||||
chr22:35325098
|
T | C | 9 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+1184T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325098 | ||||||
chr22:35325172
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.648+1258G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325172 | ||||||
chr22:35325218
|
C | T | 2 | a0001c0003t0001g0303a0001c0003t0001g0307 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.648+1304C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325218 | ||||||
chr22:35325285
|
G | A | 2 | a0001c0003t0001g0303a0001c0003t0001g0307 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.648+1371G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325285 | ||||||
chr22:35325495
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.648+1581G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325495 | ||||||
chr22:35325742
|
T | C | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0272 | 3 | HG01261.hp2 HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.649-1529T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325742 | ||||||
chr22:35325761
|
T | G | 2 | a0001c0003t0001g0303a0001c0003t0001g0307 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.649-1510T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325761 | ||||||
chr22:35325796
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1475A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325796 | ||||||
chr22:35325857
|
A | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 42 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-1414A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325857 | ||||||
chr22:35326018
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0031others(56): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.649-1253G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326018 | ||||||
chr22:35326133
|
T | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0039others(25): Show | 30 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.649-1138T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326133 | ||||||
chr22:35326358
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.649-913C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326358 | ||||||
chr22:35326444
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0050a0001c0002t0001g0051 | 5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-827C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326444 | ||||||
chr22:35326452
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.649-819C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326452 | ||||||
chr22:35326470
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.649-801T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326470 | ||||||
chr22:35326590
|
G | A | 2 | a0001c0002t0001g0154a0001c0002t0001g0155 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.649-681G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326590 | ||||||
chr22:35326668
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0143 | 3 | NA18975.hp1 NA19012.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.649-603G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326668 | ||||||
chr22:35326688
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0151 | 2 | HG02132.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.649-583G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326688 | ||||||
chr22:35326757
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.649-514C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326757 | ||||||
chr22:35326822
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.649-449G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326822 | ||||||
chr22:35327238
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.649-33G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35327238 | ||||||
chr22:35327252
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0256a0001c0002t0001g0130 | 3 | HG02148.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.649-19G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35327252 | ||||||
chr22:35327456
|
C | G | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.765+69C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327456 | ||||||
chr22:35327457
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.765+70A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327457 | ||||||
chr22:35327559
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.765+172G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327559 | ||||||
chr22:35327635
|
A | G | 1 | a0005c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.765+248A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327635 | ||||||
chr22:35327660
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.765+273T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327660 | ||||||
chr22:35327725
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(2): Show | 7 | HG02027.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+338C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327725 | ||||||
chr22:35327746
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01256.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.765+359A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327746 | ||||||
chr22:35327757
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.765+370G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327757 | ||||||
chr22:35327827
|
G | A | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.765+440G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327827 | ||||||
chr22:35327838
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 288 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.765+451A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327838 | ||||||
chr22:35327862
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.765+475A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327862 | ||||||
chr22:35327877
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG00621.hp2 HG02155.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+490C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327877 | ||||||
chr22:35328131
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.765+744C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328131 | ||||||
chr22:35328238
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.765+851C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328238 | ||||||
chr22:35328260
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.765+873G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328260 | ||||||
chr22:35328271
|
G | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0054others(20): Show | 27 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.765+884G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328271 | ||||||
chr22:35328293
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0031others(32): Show | 39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.765+906G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328293 | ||||||
chr22:35328430
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.765+1043C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328430 | ||||||
chr22:35328491
|
C | T | 2 | a0001c0003t0002g0300a0001c0003t0002g0301 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.765+1104C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328491 | ||||||
chr22:35328504
|
A | T | 1 | a0001c0004t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.765+1117A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328504 | ||||||
chr22:35328511
|
G | A | 1 | a0001c0004t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.765+1124G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328511 | ||||||
chr22:35328539
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0058 | 3 | HG01175.hp2 HG01257.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.765+1152G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328539 | ||||||
chr22:35328666
|
C | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 137 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.765+1279C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328666 | ||||||
chr22:35328808
|
G | A | 2 | a0001c0002t0001g0154a0001c0002t0001g0155 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.765+1421G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328808 | ||||||
chr22:35328822
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 14 | HG00621.hp2 HG01175.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.765+1435G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328822 | ||||||
chr22:35328856
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.765+1469C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328856 | ||||||
chr22:35328857
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.765+1470A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328857 | ||||||
chr22:35328901
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.766-1446C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328901 | ||||||
chr22:35328978
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0119others(1): Show | 4 | HG01074.hp2 HG01928.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-1369C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328978 | ||||||
chr22:35329207
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0143others(1): Show | 6 | HG02293.hp2 NA18974.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1140C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329207 | ||||||
chr22:35329545
|
A | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0031others(56): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.766-802A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329545 | ||||||
chr22:35329656
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.766-691A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329656 | ||||||
chr22:35329734
|
T | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0209others(1): Show | 4 | HG00544.hp2 HG00673.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-613T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329734 | ||||||
chr22:35329801
|
G | A | 14 | a0001c0001t0001g0171a0001c0001t0001g0191a0001c0002t0001g0009others(11): Show | 16 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.766-546G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329801 | ||||||
chr22:35329813
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(4): Show | 9 | HG01175.hp1 HG02027.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-534G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329813 | ||||||
chr22:35330030
|
A | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0170 | 3 | NA18943.hp1 NA18970.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.766-317A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330030 | ||||||
chr22:35330144
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.766-203C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330144 | ||||||
chr22:35330287
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.766-60A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330287 | ||||||
chr22:35330294
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.766-53C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330294 | ||||||
chr22:35330792
|
G | A | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.899+312G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330792 | ||||||
chr22:35330821
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.899+341C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330821 | ||||||
chr22:35330842
|
G | A | 2 | a0001c0002t0001g0230a0001c0002t0001g0236 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.899+362G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330842 | ||||||
chr22:35331093
|
C | CT | 57 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.899+633dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | |||||
chr22:35331093
|
C | CTT | 5 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(2): Show | 7 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+632_899+633dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | |||||
chr22:35331093
|
CT | C | 15 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0058others(12): Show | 15 | HG01099.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.899+633delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | |||||
chr22:35331093
|
CTT | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0171a0001c0001t0001g0191others(10): Show | 15 | HG01169.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.899+632_899+633del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | |||||
chr22:35331161
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0159 | 2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.899+681T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331161 | ||||||
chr22:35331272
|
CT | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 13 | HG01175.hp1 HG02027.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.899+805delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331272 | |||||
chr22:35331510
|
C | G | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.899+1030C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331510 | ||||||
chr22:35331983
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00642.hp2 HG02148.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.900-998G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331983 | ||||||
chr22:35331985
|
A | G | 1 | a0001c0002t0001g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.900-996A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331985 | ||||||
chr22:35332106
|
C | T | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900-875C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332106 | ||||||
chr22:35332150
|
G | T | 2 | a0001c0003t0001g0303a0001c0003t0001g0307 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-831G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332150 | ||||||
chr22:35332293
|
A | G | 1 | a0001c0010t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.900-688A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332293 | ||||||
chr22:35332362
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.900-619G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332362 | ||||||
chr22:35332473
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(150): Show | 182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.900-508T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332473 | ||||||
chr22:35332554
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0002g0299 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.900-427G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332554 | ||||||
chr22:35332597
|
CACACACA others(3): Show |
C | 123 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.900-374_900-365del others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332597 | |||||
chr22:35332599
|
CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0038a0001c0001t0001g0144a0001c0001t0001g0171others(2): Show | 5 | HG03098.hp2 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.900-374_900-367del others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332599 | |||||
chr22:35332605
|
CAT | C | 56 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(53): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.900-374_900-373del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332605 | |||||
chr22:35332607
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(3): Show | 8 | HG01993.hp1 HG02027.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.900-374T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332607 | ||||||
chr22:35332676
|
A | T | 2 | a0001c0003t0001g0303a0001c0003t0001g0307 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-305A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332676 | ||||||
chr22:35332714
|
A | G | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.900-267A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332714 | ||||||
chr22:35332810
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.900-171A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332810 | ||||||
chr22:35332883
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.900-98G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332883 | ||||||
chr22:35333282
|
T | A | 12 | a0001c0001t0001g0171a0001c0001t0001g0191a0001c0002t0001g0009others(9): Show | 14 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-122T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 9/14 | chr22 | 35333282 | ||||||
chr22:35333316
|
G | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0125others(2): Show | 7 | HG00597.hp2 NA18971.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.934-88G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 9/14 | chr22 | 35333316 | ||||||
chr22:35333588
|
A | G | 2 | a0001c0004t0001g0245a0001c0004t0001g0250 | 2 | HG01099.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1027+91A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333588 | ||||||
chr22:35333614
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0115a0001c0001t0001g0147others(4): Show | 9 | HG00558.hp2 HG02040.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+117C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333614 | ||||||
chr22:35333660
|
G | A | 2 | a0001c0004t0001g0245a0001c0004t0001g0250 | 2 | HG01099.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1027+163G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333660 | ||||||
chr22:35333673
|
C | T | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1027+176C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333673 | ||||||
chr22:35333677
|
C | A | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1027+180C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333677 | ||||||
chr22:35333728
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1027+231G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333728 | ||||||
chr22:35333743
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1027+246A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333743 | ||||||
chr22:35333849
|
G | A | 2 | a0001c0013t0001g0308a0001c0014t0001g0309 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1027+352G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333849 | ||||||
chr22:35333853
|
A | C | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1027+356A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333853 | ||||||
chr22:35333949
|
C | G | 1 | a0001c0002t0001g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1028-379C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333949 | ||||||
chr22:35334092
|
A | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(180): Show | 218 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1028-236A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334092 | ||||||
chr22:35334104
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0204 | 3 | HG02015.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1028-224C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334104 | ||||||
chr22:35334197
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1028-131C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334197 | ||||||
chr22:35334200
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1028-128G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334200 | ||||||
chr22:35334204
|
A | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0050a0001c0002t0001g0051 | 5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-124A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334204 | ||||||
chr22:35334261
|
T | C | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1028-67T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334261 | ||||||
chr22:35334616
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1148+168T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334616 | ||||||
chr22:35334771
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1148+323A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334771 | ||||||
chr22:35334786
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148+338G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334786 | ||||||
chr22:35334841
|
C | A | 1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1148+393C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334841 | ||||||
chr22:35334841
|
C | G | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1148+393C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334841 | ||||||
chr22:35334850
|
A | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1148+402A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334850 | ||||||
chr22:35334862
|
A | C | 6 | a0001c0001t0002g0297a0001c0002t0001g0172a0001c0002t0002g0296others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+414A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334862 | ||||||
chr22:35334993
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG00438.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1148+545C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334993 | ||||||
chr22:35335101
|
G | A | 117 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(114): Show | 143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1148+653G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335101 | ||||||
chr22:35335109
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0039others(24): Show | 30 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1148+661C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335109 | ||||||
chr22:35335182
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0110a0001c0001t0001g0138others(4): Show | 10 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1148+734G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335182 | ||||||
chr22:35335252
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(252): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1148+804T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335252 | ||||||
chr22:35335411
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0002g0297others(1): Show | 4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+963G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335411 | ||||||
chr22:35335652
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1148+1204C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335652 | ||||||
chr22:35335653
|
G | A | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1148+1205G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335653 | ||||||
chr22:35335668
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1148+1220G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335668 | ||||||
chr22:35335680
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1148+1232C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335680 | ||||||
chr22:35335704
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1148+1256G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335704 | ||||||
chr22:35335762
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1148+1314G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335762 | ||||||
chr22:35335774
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+1326T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335774 | ||||||
chr22:35335929
|
G | A | 1 | a0005c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1148+1481G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335929 | ||||||
chr22:35335964
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0002g0297others(1): Show | 4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+1516G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335964 | ||||||
chr22:35336193
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1148+1745G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336193 | ||||||
chr22:35336257
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1148+1809G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336257 | ||||||
chr22:35336307
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1148+1859G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336307 | ||||||
chr22:35336574
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1148+2126G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336574 | ||||||
chr22:35336610
|
C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 98 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1149-2103C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336610 | ||||||
chr22:35336704
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1149-2009C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336704 | ||||||
chr22:35336847
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1149-1866C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336847 | ||||||
chr22:35336864
|
C | T | 4 | a0001c0002t0001g0190a0001c0002t0001g0215a0001c0002t0001g0234others(1): Show | 4 | HG01106.hp1 HG01192.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-1849C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336864 | ||||||
chr22:35336911
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1149-1802G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336911 | ||||||
chr22:35336942
|
CT | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1149-1755delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr22 | 35336942 | |||||
chr22:35337000
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1149-1713G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337000 | ||||||
chr22:35337082
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149-1631G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337082 | ||||||
chr22:35337093
|
C | T | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1149-1620C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337093 | ||||||
chr22:35337180
|
C | T | 2 | a0001c0002t0001g0186a0001c0002t0001g0222 | 2 | HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1149-1533C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337180 | ||||||
chr22:35337259
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1149-1454T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337259 | ||||||
chr22:35337311
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1149-1402A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337311 | ||||||
chr22:35337314
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-1399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337314 | ||||||
chr22:35337343
|
G | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1149-1370G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337343 | ||||||
chr22:35337399
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(8): Show | 13 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-1314C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337399 | ||||||
chr22:35337462
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0162 | 2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1149-1251G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337462 | ||||||
chr22:35337661
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(107): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1149-1052G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337661 | ||||||
chr22:35337715
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1149-998C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337715 | ||||||
chr22:35337729
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(8): Show | 13 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-984G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337729 | ||||||
chr22:35337929
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1149-784G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337929 | ||||||
chr22:35338109
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-604G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338109 | ||||||
chr22:35338154
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-559A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338154 | ||||||
chr22:35338265
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149-448C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338265 | ||||||
chr22:35338314
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1149-399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338314 | ||||||
chr22:35338429
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-284A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338429 | ||||||
chr22:35338638
|
C | T | 1 | a0001c0006t0001g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149-75C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338638 | ||||||
chr22:35339062
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1224+274G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339062 | ||||||
chr22:35339108
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1224+320A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339108 | ||||||
chr22:35339366
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1224+578G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339366 | ||||||
chr22:35339615
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1224+827C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339615 | ||||||
chr22:35339661
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1224+873T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339661 | ||||||
chr22:35339711
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1224+923C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339711 | ||||||
chr22:35339732
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1224+944G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339732 | ||||||
chr22:35339759
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0171a0001c0001t0001g0191others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+971C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339759 | ||||||
chr22:35339767
|
G | A | 216 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(213): Show | 257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1224+979G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339767 | ||||||
chr22:35339844
|
C | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0065a0001c0001t0001g0107others(4): Show | 7 | HG02135.hp1 HG02523.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.1224+1056C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339844 | ||||||
chr22:35339898
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1224+1110C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339898 | ||||||
chr22:35339903
|
CA | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1224+1129delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35339903 | |||||
chr22:35339910
|
A | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0053others(13): Show | 20 | HG00438.hp1 HG00558.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1224+1122A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339910 | ||||||
chr22:35339928
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1224+1140T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339928 | ||||||
chr22:35340144
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0208a0001c0002t0002g0304 | 4 | HG03195.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+1356G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340144 | ||||||
chr22:35340209
|
G | C | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1224+1421G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340209 | ||||||
chr22:35340233
|
C | CGAGGAGG others(3): Show |
1 | a0001c0001t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1224+1455_1224+146 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35340233 | |||||
chr22:35340315
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0171a0001c0001t0001g0191others(2): Show | 5 | HG02976.hp1 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+1527G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340315 | ||||||
chr22:35340434
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1224+1646A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340434 | ||||||
chr22:35340715
|
C | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0037others(17): Show | 24 | HG00438.hp1 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1224+1927C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340715 | ||||||
chr22:35340738
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0138 | 4 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+1950C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340738 | ||||||
chr22:35340827
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1224+2039C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340827 | ||||||
chr22:35341221
|
C | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1224+2433C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341221 | ||||||
chr22:35341229
|
A | C | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2441A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341229 | ||||||
chr22:35341252
|
A | G | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2464A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341252 | ||||||
chr22:35341253
|
C | A | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2465C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341253 | ||||||
chr22:35341302
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1224+2514G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341302 | ||||||
chr22:35341348
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1224+2560C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341348 | ||||||
chr22:35341399
|
C | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0277 | 3 | HG02074.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1224+2611C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341399 | ||||||
chr22:35341468
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1224+2680G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341468 | ||||||
chr22:35341539
|
C | T | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2751C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341539 | ||||||
chr22:35341582
|
C | T | 1 | a0001c0002t0001g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1224+2794C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341582 | ||||||
chr22:35341583
|
G | A | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1224+2795G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341583 | ||||||
chr22:35341732
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1224+2944T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341732 | ||||||
chr22:35341746
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1224+2958C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341746 | ||||||
chr22:35341825
|
C | T | 2 | a0001c0001t0001g0092a0001c0002t0001g0103 | 2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1224+3037C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341825 | ||||||
chr22:35342038
|
G | GGCTGAAG others(34): Show |
1 | a0001c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1224+3251_1224+329 others(45): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342038 | |||||
chr22:35342222
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1224+3434G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342222 | ||||||
chr22:35342293
|
G | A | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1225-3432G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342293 | ||||||
chr22:35342390
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1225-3335C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342390 | ||||||
chr22:35342412
|
A | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0037others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-3313A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342412 | ||||||
chr22:35342495
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(215): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1225-3230C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342495 | ||||||
chr22:35342554
|
G | GGGATCCT others(3): Show |
17 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 19 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1225-3167_1225-315 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342554 | |||||
chr22:35342593
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3132T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342593 | ||||||
chr22:35342609
|
T | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3116T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342609 | ||||||
chr22:35342627
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3098T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342627 | ||||||
chr22:35342638
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3087A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342638 | ||||||
chr22:35342643
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3082T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342643 | ||||||
chr22:35342646
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3079T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342646 | ||||||
chr22:35342661
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3064T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342661 | ||||||
chr22:35342669
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3056A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342669 | ||||||
chr22:35342681
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3044T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342681 | ||||||
chr22:35342687
|
C | A | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1225-3038C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342687 | ||||||
chr22:35342688
|
T | C | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1225-3037T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342688 | ||||||
chr22:35342727
|
C | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2998C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342727 | ||||||
chr22:35342728
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2997A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342728 | ||||||
chr22:35342729
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2996C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342729 | ||||||
chr22:35342733
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2992A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342733 | ||||||
chr22:35342741
|
C | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2984C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342741 | ||||||
chr22:35342743
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2982A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342743 | ||||||
chr22:35342750
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2975T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342750 | ||||||
chr22:35342751
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2974A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342751 | ||||||
chr22:35342753
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2972A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342753 | ||||||
chr22:35342755
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2970A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342755 | ||||||
chr22:35342766
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2959A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342766 | ||||||
chr22:35342768
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2957A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342768 | ||||||
chr22:35342774
|
A | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2951A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342774 | ||||||
chr22:35342775
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2950C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342775 | ||||||
chr22:35342776
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2949A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342776 | ||||||
chr22:35342777
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2948C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342777 | ||||||
chr22:35342780
|
ACCACACA others(5): Show |
A | 3 | a0001c0001t0001g0121a0001c0001t0001g0149a0001c0001t0001g0262 | 3 | HG02074.hp2 NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1225-2932_1225-292 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342780 | |||||
chr22:35342795
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2930A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342795 | ||||||
chr22:35342804
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2921T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342804 | ||||||
chr22:35342807
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2918A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342807 | ||||||
chr22:35342815
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2910A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342815 | ||||||
chr22:35342825
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2900A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342825 | ||||||
chr22:35342829
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2896C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342829 | ||||||
chr22:35342832
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2893T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342832 | ||||||
chr22:35342838
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2887C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342838 | ||||||
chr22:35342843
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2882C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342843 | ||||||
chr22:35342844
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2881A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342844 | ||||||
chr22:35342854
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2871A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342854 | ||||||
chr22:35342857
|
C | G | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1225-2868C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342857 | ||||||
chr22:35342868
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2857A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342868 | ||||||
chr22:35342870
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2855A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342870 | ||||||
chr22:35342882
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2843A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342882 | ||||||
chr22:35342886
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2839C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342886 | ||||||
chr22:35342887
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2838A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342887 | ||||||
chr22:35342889
|
ACACACAT others(34): Show |
A | 1 | a0001c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1225-2834_1225-279 others(45): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342889 | |||||
chr22:35342912
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2813A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342912 | ||||||
chr22:35342917
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2808T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342917 | ||||||
chr22:35342922
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2803A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342922 | ||||||
chr22:35342925
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2800T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342925 | ||||||
chr22:35342929
|
A | G | 32 | a0001c0002t0001g0016a0001c0002t0001g0023a0001c0002t0001g0024others(29): Show | 37 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1225-2796A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342929 | ||||||
chr22:35342932
|
T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2793T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342932 | ||||||
chr22:35342935
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2790A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342935 | ||||||
chr22:35342943
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1225-2782A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342943 | ||||||
chr22:35342949
|
A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2776A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342949 | ||||||
chr22:35342953
|
A | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2772A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342953 | ||||||
chr22:35342954
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2771C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342954 | ||||||
chr22:35342955
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-2770C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342955 | ||||||
chr22:35342956
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2769C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342956 | ||||||
chr22:35342959
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2766A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342959 | ||||||
chr22:35342961
|
A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2764A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342961 | ||||||
chr22:35342963
|
ACAC | A | 177 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(174): Show | 207 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.1225-2758_1225-275 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342963 | |||||
chr22:35342978
|
ACT | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(87): Show | 98 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1225-2745_1225-274 others(6): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342978 | |||||
chr22:35343022
|
C | T | 92 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0005others(89): Show | 114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1225-2703C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343022 | ||||||
chr22:35343072
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2653G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343072 | ||||||
chr22:35343104
|
ACCACACA others(3): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2609_1225-260 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343104 | |||||
chr22:35343105
|
CCA | C | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-2612_1225-261 others(6): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343105 | |||||
chr22:35343117
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1225-2608A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343117 | ||||||
chr22:35343122
|
C | CAACACAC others(99): Show |
1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2602_1225-260 others(110): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343122 | |||||
chr22:35343132
|
ACAC | A | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-2592_1225-259 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343132 | ||||||
chr22:35343134
|
ACAT | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0077others(2): Show | 7 | HG00597.hp2 NA18971.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-2589_1225-258 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343134 | |||||
chr22:35343136
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2589A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343136 | ||||||
chr22:35343137
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2588T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343137 | ||||||
chr22:35343158
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2567T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343158 | ||||||
chr22:35343165
|
A | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2560A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343165 | ||||||
chr22:35343167
|
C | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2558C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343167 | ||||||
chr22:35343174
|
A | C | 2 | a0001c0002t0001g0023a0001c0002t0001g0243 | 3 | HG00642.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1225-2551A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343174 | ||||||
chr22:35343187
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2538C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343187 | ||||||
chr22:35343188
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2537T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343188 | ||||||
chr22:35343189
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1225-2536C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343189 | ||||||
chr22:35343193
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2532T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343193 | ||||||
chr22:35343195
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2530A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343195 | ||||||
chr22:35343196
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2529T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343196 | ||||||
chr22:35343199
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2526G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343199 | ||||||
chr22:35343202
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2523T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343202 | ||||||
chr22:35343203
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2522A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343203 | ||||||
chr22:35343204
|
CACACACA others(5): Show |
C | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-2511_1225-250 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343204 | |||||
chr22:35343216
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2509T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343216 | ||||||
chr22:35343253
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2472A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343253 | ||||||
chr22:35343254
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2471C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343254 | ||||||
chr22:35343270
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2455C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343270 | ||||||
chr22:35343294
|
T | TACACACC others(116): Show |
1 | a0001c0002t0001g0246 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225-2421_1225-242 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343294 | |||||
chr22:35343305
|
C | CCTACACA others(116): Show |
195 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | |||||
chr22:35343305
|
C | CCTACACA others(116): Show |
1 | a0001c0002t0001g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | |||||
chr22:35343305
|
C | CCTACACA others(114): Show |
17 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 19 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1225-2353_1225-235 others(125): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | |||||
chr22:35343305
|
C | CCTACACA others(112): Show |
87 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(84): Show | 93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1225-2384_1225-238 others(123): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | |||||
chr22:35343305
|
C | G | 2 | a0001c0001t0001g0196a0001c0002t0001g0246 | 2 | HG02965.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1225-2420C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343305 | ||||||
chr22:35343334
|
A | ACACACAC others(116): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343334 | |||||
chr22:35343336
|
A | ACACACCA others(108): Show |
1 | a0001c0001t0001g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1225-2384_1225-238 others(119): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343336 | |||||
chr22:35343437
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1225-2288A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343437 | ||||||
chr22:35343518
|
T | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0037others(15): Show | 22 | HG00558.hp2 HG02040.hp2 HG02976.hp1 others(19): Show |
intron_variant | MODIFIER | c.1225-2207T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343518 | ||||||
chr22:35343584
|
ACCTACAC others(5): Show |
A | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01891.hp1 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1225-2128_1225-211 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343584 | |||||
chr22:35343678
|
ACAC | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(4): Show | 9 | HG00544.hp2 HG00673.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-2043_1225-204 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343678 | |||||
chr22:35343731
|
CCCA | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1989_1225-198 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343731 | |||||
chr22:35343736
|
C | CACACCTA others(20): Show |
89 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(86): Show | 97 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1225-1972_1225-197 others(31): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343736 | |||||
chr22:35343736
|
C | CGCACCTA others(20): Show |
1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1225-1989_1225-198 others(31): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343736 | ||||||
chr22:35343761
|
CTACACA | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044 | 5 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1957_1225-195 others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343761 | |||||
chr22:35343807
|
C | A | 88 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0005others(85): Show | 110 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1225-1918C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343807 | ||||||
chr22:35343866
|
C | A | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1225-1859C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343866 | ||||||
chr22:35343934
|
A | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(87): Show | 98 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1225-1791A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343934 | ||||||
chr22:35343941
|
CTACACAC others(6): Show |
C | 2 | a0001c0002t0001g0230a0001c0002t0001g0236 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1225-1779_1225-176 others(17): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343941 | |||||
chr22:35344004
|
TACACCTA others(5): Show |
T | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-1710_1225-169 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35344004 | |||||
chr22:35344055
|
A | C | 3 | a0001c0002t0001g0172a0001c0002t0002g0296a0001c0002t0002g0298 | 3 | HG01069.hp2 HG01071.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1225-1670A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344055 | ||||||
chr22:35344081
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1225-1644G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344081 | ||||||
chr22:35344135
|
G | A | 97 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0002t0001g0001others(94): Show | 121 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1225-1590G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344135 | ||||||
chr22:35344171
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1225-1554C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344171 | ||||||
chr22:35344210
|
G | A | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-1515G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344210 | ||||||
chr22:35344278
|
A | C | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01891.hp1 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1225-1447A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344278 | ||||||
chr22:35344281
|
C | T | 7 | a0001c0001t0001g0135a0001c0001t0001g0217a0001c0001t0001g0273others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-1444C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344281 | ||||||
chr22:35344324
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-1401G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344324 | ||||||
chr22:35344354
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(10): Show | 15 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1225-1371G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344354 | ||||||
chr22:35344449
|
C | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(84): Show | 93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1225-1276C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344449 | ||||||
chr22:35344494
|
C | T | 2 | a0001c0002t0001g0257a0001c0002t0001g0280 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1225-1231C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344494 | ||||||
chr22:35344496
|
G | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0002g0297 | 3 | HG02818.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1225-1229G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344496 | ||||||
chr22:35344533
|
G | T | 1 | a0001c0002t0001g0275 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1225-1192G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344533 | ||||||
chr22:35344650
|
G | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0037others(15): Show | 22 | HG00558.hp2 HG02040.hp2 HG02976.hp1 others(19): Show |
intron_variant | MODIFIER | c.1225-1075G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344650 | ||||||
chr22:35344707
|
CTCTG | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0115a0001c0001t0001g0203others(2): Show | 7 | HG00558.hp2 HG03654.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225-1010_1225-100 others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35344707 | |||||
chr22:35344843
|
A | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0002g0297others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-882A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344843 | ||||||
chr22:35344873
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(10): Show | 15 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1225-852G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344873 | ||||||
chr22:35344899
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1225-826T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344899 | ||||||
chr22:35345041
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225-684C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345041 | ||||||
chr22:35345042
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG00597.hp1 NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1225-683G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345042 | ||||||
chr22:35345088
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-637G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345088 | ||||||
chr22:35345145
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1225-580C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345145 | ||||||
chr22:35345172
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1225-553T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345172 | ||||||
chr22:35345178
|
T | C | 224 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(221): Show | 260 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1225-547T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345178 | ||||||
chr22:35345346
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-379C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345346 | ||||||
chr22:35345818
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1284+34G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345818 | ||||||
chr22:35345823
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1284+39A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345823 | ||||||
chr22:35345827
|
G | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(79): Show | 88 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1284+43G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345827 | ||||||
chr22:35345870
|
A | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(226): Show | 265 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1284+86A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345870 | ||||||
chr22:35346002
|
C | T | 1 | a0005c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1284+218C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346002 | ||||||
chr22:35346075
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284+291C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346075 | ||||||
chr22:35346110
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0294 | 3 | HG01175.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1284+326G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346110 | ||||||
chr22:35346360
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0091a0001c0001t0001g0181others(2): Show | 6 | HG00621.hp1 NA18612.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-570G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346360 | ||||||
chr22:35346492
|
C | T | 1 | a0001c0002t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1285-438C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346492 | ||||||
chr22:35346531
|
C | T | 187 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(184): Show | 217 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1285-399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346531 | ||||||
chr22:35346625
|
G | A | 3 | a0001c0003t0002g0300a0001c0003t0002g0301a0001c0014t0001g0309 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1285-305G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346625 | ||||||
chr22:35346769
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0044others(7): Show | 12 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-161C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346769 |