geneid | 23788 |
---|---|
ensemblid | ENSG00000109919.10 |
hgncid | 17587 |
symbol | MTCH2 |
name | mitochondrial carrier 2 |
refseq_nuc | NM_014342.4 |
refseq_prot | NP_055157.1 |
ensembl_nuc | ENST00000302503.8 |
ensembl_prot | ENSP00000303222.3 |
mane_status | MANE Select |
chr | chr11 |
start | 47617317 |
end | 47642559 |
strand | - |
ver | v1.2 |
region | chr11:47617317-47642559 |
region5000 | chr11:47612317-47647559 |
regionname0 | MTCH2_chr11_47617317_47642559 |
regionname5000 | MTCH2_chr11_47612317_47647559 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 303 | 279 | 84 | 43 | 114 | 10 | 26 | 89 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0002 | 0/0 | 303 | 88 | 5 | 21 | 46 | 2 | 14 | 41 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0003 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0004 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0005 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 912 | 279 | 84 | 43 | 114 | 10 | 26 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
c0002 | 0/0 | 912 | 88 | 5 | 21 | 46 | 2 | 14 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
c0003 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
c0004 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
c0005 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1611 | 325 | 56 | 59 | 158 | 11 | 40 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0002 | 0/0 | 1611 | 16 | 16 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0003 | 0/0 | 1611 | 6 | 0 | 3 | 0 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0004 | 0/0 | 1611 | 5 | 5 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0005 | 1/0 | 1611 | 5 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0006 | 0/0 | 1611 | 4 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0007 | 0/0 | 1607 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0008 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0009 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0010 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0011 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0012 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
t0013 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 1 | 1 | 9 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0002 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0003 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0007 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 912 | 279 | 84 | 43 | 114 | 10 | 26 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0002c0002 | 0/0 | 912 | 88 | 5 | 21 | 46 | 2 | 14 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0003c0004 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0004c0005 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0005c0003 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2522 | 235 | 50 | 38 | 113 | 9 | 24 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0002 | 0/0 | 2522 | 16 | 16 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0003 | 0/0 | 2522 | 6 | 0 | 3 | 0 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0004 | 0/0 | 2522 | 5 | 5 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0005 | 1/0 | 2522 | 5 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0006 | 0/0 | 2522 | 4 | 4 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0007 | 0/0 | 2518 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0008 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0010 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0011 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0012 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0001c0001t0013 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0002c0002t0001 | 0/0 | 2522 | 87 | 5 | 21 | 45 | 2 | 14 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0002c0002t0009 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0003c0004t0001 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0004c0005t0001 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
a0005c0003t0001 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | copy fasta | chr11 | 47612317 | 47647559 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 1 | 1 | 9 | 1 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0007 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0005g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0008g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0010g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0012g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0001c0001t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0002c0002t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0003c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0004c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
a0005c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0041 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0027 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01168 | hp2 | a0001 | c0001 | t0013 | g0302 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0103 | EUR | IBS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02451 | hp2 | a0005 | c0003 | t0001 | g0118 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0249 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0036 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02735 | hp2 | a0003 | c0004 | t0001 | g0268 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0138 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03017 | hp2 | a0004 | c0005 | t0001 | g0299 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | GWD | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0314 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | CHB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18961 | hp1 | a0002 | c0002 | t0009 | g0113 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18993 | hp1 | a0001 | c0001 | t0010 | g0173 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0221 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | GIH | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0029 | REF | REF | MTCH2_chr11_47612317_47647559 | MTCH2 | chr11 | 47612317 | 47647559 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47618877
|
G | C | 1 | a0002 | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
missense_variant | MODERATE | c.868C>G | p.Pro290Ala | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 962/2522 | 868/912 | 290/303 | chr11 | 47618877 | ||
chr11:47622717
|
C | T | 1 | a0003 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.809G>A | p.Cys270Tyr | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/13 | 903/2522 | 809/912 | 270/303 | chr11 | 47622717 | ||
chr11:47630596
|
T | C | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.498A>G | p.Ile166Met | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/13 | 592/2522 | 498/912 | 166/303 | chr11 | 47630596 | ||
chr11:47638776
|
G | T | 1 | a0005 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.202C>A | p.Arg68Ser | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/13 | 296/2522 | 202/912 | 68/303 | chr11 | 47638776 |
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 |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47617458
|
C | A | 2 | a0001c0001t0002a0001c0001t0006 | 20 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1375G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1375 | chr11 | 47617458 | |||||
chr11:47617479
|
A | G | 1 | a0002c0002t0009 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1354 | chr11 | 47617479 | |||||
chr11:47617511
|
G | A | 1 | a0001c0001t0003 | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1322 | chr11 | 47617511 | |||||
chr11:47617601
|
A | C | 1 | a0001c0001t0002 | 16 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1232T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 1232 | chr11 | 47617601 | |||||
chr11:47617861
|
T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 972 | chr11 | 47617861 | |||||
chr11:47617973
|
T | G | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*860A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 860 | chr11 | 47617973 | |||||
chr11:47618006
|
G | C | 1 | a0001c0001t0011 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 827 | chr11 | 47618006 | |||||
chr11:47618042
|
C | G | 2 | a0001c0001t0004a0001c0001t0007 | 8 | HG02647.hp2 HG02809.hp2 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*791G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 791 | chr11 | 47618042 | |||||
chr11:47618073
|
CCTTT | C | 1 | a0001c0001t0007 | 3 | HG02809.hp2 HG02897.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*756_*759delAAAG | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 756 | chr11 | 47618073 | |||||
chr11:47618178
|
T | A | 1 | a0001c0001t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 655 | chr11 | 47618178 | |||||
chr11:47618581
|
T | C | 1 | a0001c0001t0013 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 252 | chr11 | 47618581 | |||||
chr11:47618649
|
G | A | 1 | a0001c0001t0003 | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 13/13 | 184 | chr11 | 47618649 | |||||
chr11:47642484
|
A | C | 1 | a0001c0001t0008 | 1 | HG01168.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/13 | 19 | chr11 | 47642484 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47619109
|
T | C | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.826-190A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619109 | ||||||
chr11:47619210
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0125others(3): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.826-291A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619210 | ||||||
chr11:47619316
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.826-397T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619316 | ||||||
chr11:47619339
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 109 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.826-420G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619339 | ||||||
chr11:47619470
|
G | A | 1 | a0002c0002t0001g0106 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.826-551C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619470 | ||||||
chr11:47619623
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.826-704A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619623 | ||||||
chr11:47619681
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.826-762G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619681 | ||||||
chr11:47619915
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0312 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.826-996T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47619915 | ||||||
chr11:47620002
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.826-1083C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620002 | ||||||
chr11:47620021
|
G | A | 1 | a0002c0002t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.826-1102C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620021 | ||||||
chr11:47620031
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826-1112G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620031 | ||||||
chr11:47620071
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.826-1152G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620071 | ||||||
chr11:47620195
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0133 | 2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.826-1276C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620195 | ||||||
chr11:47620326
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826-1407C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620326 | ||||||
chr11:47620335
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0200others(4): Show | 8 | HG00408.hp1 NA18947.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.826-1416C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620335 | ||||||
chr11:47620346
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.826-1427C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620346 | ||||||
chr11:47620666
|
A | G | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0246others(5): Show | 10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.826-1747T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620666 | ||||||
chr11:47620677
|
A | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.826-1758T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620677 | ||||||
chr11:47620845
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(18): Show | 24 | HG00544.hp1 HG02083.hp2 HG02148.hp2 others(21): Show |
intron_variant | MODIFIER | c.825+1856G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47620845 | ||||||
chr11:47621021
|
A | G | 1 | a0002c0002t0001g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.825+1680T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621021 | ||||||
chr11:47621436
|
CT | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.825+1264delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621436 | ||||||
chr11:47621581
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0312 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.825+1120G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47621581 | ||||||
chr11:47622059
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0245 | 3 | HG02258.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.825+642A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622059 | ||||||
chr11:47622297
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.825+404T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622297 | ||||||
chr11:47622339
|
T | A | 97 | a0001c0001t0001g0021a0001c0001t0001g0233a0001c0001t0001g0234others(94): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.825+362A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 12/12 | chr11 | 47622339 | ||||||
chr11:47622853
|
A | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG03704.hp1 HG03834.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-77T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47622853 | ||||||
chr11:47623258
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.750-482C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623258 | ||||||
chr11:47623369
|
CT | C | 121 | a0001c0001t0001g0021a0001c0001t0001g0126a0001c0001t0001g0151others(118): Show | 123 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.750-594delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623369 | ||||||
chr11:47623375
|
T | A | 16 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0023others(13): Show | 19 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.750-599A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | ||||||
chr11:47623375
|
T | TA | 8 | a0001c0001t0001g0024a0001c0001t0001g0201a0001c0001t0001g0258others(5): Show | 9 | HG01106.hp1 HG01346.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.750-600_750-599ins others(1): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | ||||||
chr11:47623375
|
TTA | T | 9 | a0001c0001t0001g0150a0001c0001t0003g0219a0002c0002t0001g0036others(6): Show | 9 | HG00323.hp1 HG01071.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.750-601_750-600del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623375 | ||||||
chr11:47623376
|
T | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.750-600A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623376 | ||||||
chr11:47623377
|
A | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.750-601T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623377 | ||||||
chr11:47623868
|
A | G | 1 | a0001c0001t0003g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.750-1092T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623868 | ||||||
chr11:47623935
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0164a0001c0001t0001g0165 | 4 | NA18945.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.750-1159G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47623935 | ||||||
chr11:47624213
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0005c0003t0001g0118 | 3 | HG01243.hp1 HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.750-1437G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624213 | ||||||
chr11:47624231
|
C | CA | 37 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0172others(34): Show | 39 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.749+1442dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624231 | ||||||
chr11:47624231
|
CA | C | 8 | a0001c0001t0013g0302a0002c0002t0001g0035a0002c0002t0001g0037others(5): Show | 8 | HG01168.hp2 NA18939.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+1442delT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624231 | ||||||
chr11:47624262
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.749+1412G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624262 | ||||||
chr11:47624286
|
T | A | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+1388A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624286 | ||||||
chr11:47624299
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.749+1375T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624299 | ||||||
chr11:47624823
|
C | CA | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+850dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47624823 | ||||||
chr11:47625028
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.749+646G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625028 | ||||||
chr11:47625036
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.749+638G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625036 | ||||||
chr11:47625088
|
AAAAAAC | A | 109 | a0001c0001t0001g0021a0001c0001t0001g0216a0001c0001t0001g0217others(106): Show | 111 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.749+580_749+585del others(6): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625088 | ||||||
chr11:47625191
|
C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.749+483G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625191 | ||||||
chr11:47625218
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0200others(6): Show | 10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.749+456G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625218 | ||||||
chr11:47625225
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.749+449T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625225 | ||||||
chr11:47625422
|
CA | C | 120 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0119others(117): Show | 124 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.749+251delT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625422 | ||||||
chr11:47625434
|
A | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0233a0001c0001t0001g0234others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.749+240T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625434 | ||||||
chr11:47625435
|
AAT | A | 17 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0162others(14): Show | 17 | HG00544.hp2 HG01496.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.749+237_749+238del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625435 | ||||||
chr11:47625436
|
AT | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.749+237delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625436 | ||||||
chr11:47625437
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0189 | 2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.749+237A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625437 | ||||||
chr11:47625548
|
C | G | 1 | a0001c0001t0001g0025 | 2 | NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.749+126G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625548 | ||||||
chr11:47625568
|
C | G | 1 | a0002c0002t0001g0112 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.749+106G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 11/12 | chr11 | 47625568 | ||||||
chr11:47625884
|
TAC | T | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-145_682-144del others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47625884 | ||||||
chr11:47625992
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0200others(6): Show | 10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.682-251G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47625992 | ||||||
chr11:47626018
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682-277A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626018 | ||||||
chr11:47626113
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.682-372G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626113 | ||||||
chr11:47626237
|
G | A | 1 | a0002c0002t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.682-496C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626237 | ||||||
chr11:47626266
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.682-525C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626266 | ||||||
chr11:47626356
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0189 | 2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.682-615A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626356 | ||||||
chr11:47626490
|
G | A | 87 | a0002c0002t0001g0008a0002c0002t0001g0032a0002c0002t0001g0033others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.681+590C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626490 | ||||||
chr11:47626550
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.681+530T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47626550 | ||||||
chr11:47627010
|
C | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0147others(24): Show | 30 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.681+70G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 10/12 | chr11 | 47627010 | ||||||
chr11:47627357
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.634-230C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627357 | ||||||
chr11:47627628
|
A | AT | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0210others(13): Show | 19 | HG01243.hp1 HG01884.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.634-502dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627628 | ||||||
chr11:47627628
|
AT | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(3): Show | 6 | HG02896.hp2 HG03098.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.634-502delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627628 | ||||||
chr11:47627980
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.634-853A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47627980 | ||||||
chr11:47628066
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.633+887C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628066 | ||||||
chr11:47628164
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.633+789G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628164 | ||||||
chr11:47628298
|
G | A | 2 | a0002c0002t0001g0049a0002c0002t0001g0068 | 2 | NA18940.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.633+655C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628298 | ||||||
chr11:47628586
|
AT | A | 97 | a0001c0001t0001g0021a0001c0001t0001g0233a0001c0001t0001g0234others(94): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.633+366delA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628586 | ||||||
chr11:47628607
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.633+346A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628607 | ||||||
chr11:47628636
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.633+317C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628636 | ||||||
chr11:47628766
|
C | T | 1 | a0002c0002t0001g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.633+187G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 9/12 | chr11 | 47628766 | ||||||
chr11:47629076
|
C | G | 1 | a0001c0001t0006g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540-30G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629076 | ||||||
chr11:47629132
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.540-86A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629132 | ||||||
chr11:47629194
|
A | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0312 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.540-148T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629194 | ||||||
chr11:47629339
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.540-293C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629339 | ||||||
chr11:47629441
|
C | T | 110 | a0001c0001t0001g0021a0001c0001t0001g0216a0001c0001t0001g0217others(107): Show | 112 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.540-395G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629441 | ||||||
chr11:47629557
|
G | A | 1 | a0002c0002t0001g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.540-511C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629557 | ||||||
chr11:47629587
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.540-541T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629587 | ||||||
chr11:47629612
|
C | T | 1 | a0002c0002t0001g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.540-566G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629612 | ||||||
chr11:47629751
|
T | TA | 20 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 25 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.540-706dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629751 | ||||||
chr11:47629765
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.540-719G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629765 | ||||||
chr11:47629780
|
C | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0284a0001c0001t0001g0287others(2): Show | 5 | HG00438.hp1 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-734G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629780 | ||||||
chr11:47629852
|
G | T | 3 | a0002c0002t0001g0032a0002c0002t0001g0059a0002c0002t0001g0083 | 3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.539+703C>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47629852 | ||||||
chr11:47630025
|
TATTA | T | 6 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+526_539+529del others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630025 | ||||||
chr11:47630052
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539+503C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630052 | ||||||
chr11:47630287
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0224a0001c0001t0002g0225 | 4 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+268C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630287 | ||||||
chr11:47630320
|
G | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0159a0001c0001t0001g0180others(4): Show | 9 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+235C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 8/12 | chr11 | 47630320 | ||||||
chr11:47630924
|
A | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0282a0001c0001t0001g0286 | 3 | HG00639.hp2 HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.479+112T>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 7/12 | chr11 | 47630924 | ||||||
chr11:47630951
|
G | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+85C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 7/12 | chr11 | 47630951 | ||||||
chr11:47631378
|
C | T | 7 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0073others(4): Show | 7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+276G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 6/12 | chr11 | 47631378 | ||||||
chr11:47631792
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-81C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47631792 | ||||||
chr11:47631811
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.370-100A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47631811 | ||||||
chr11:47632000
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.370-289T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632000 | ||||||
chr11:47632159
|
C | T | 6 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-448G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632159 | ||||||
chr11:47632357
|
A | AT | 7 | a0001c0001t0001g0160a0001c0001t0001g0260a0001c0001t0001g0274others(4): Show | 7 | HG03688.hp2 HG03831.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-647dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632357 | ||||||
chr11:47632513
|
C | T | 4 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0087others(1): Show | 4 | HG01943.hp2 HG01975.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-802G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632513 | ||||||
chr11:47632548
|
G | A | 1 | a0002c0002t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.370-837C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632548 | ||||||
chr11:47632621
|
C | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.370-910G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632621 | ||||||
chr11:47632705
|
T | C | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-994A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632705 | ||||||
chr11:47632839
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.370-1128G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632839 | ||||||
chr11:47632890
|
T | C | 1 | a0002c0002t0001g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.370-1179A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632890 | ||||||
chr11:47632947
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1236C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47632947 | ||||||
chr11:47633114
|
C | CT | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.370-1404dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633114 | ||||||
chr11:47633114
|
C | CTT | 8 | a0001c0001t0001g0205a0001c0001t0001g0273a0001c0001t0006g0143others(5): Show | 8 | HG01433.hp1 HG02615.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1405_370-1404d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633114 | ||||||
chr11:47633210
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.369+1462G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633210 | ||||||
chr11:47633254
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.369+1418G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633254 | ||||||
chr11:47633361
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0211 | 2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.369+1311G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633361 | ||||||
chr11:47633505
|
A | AAT | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0246others(3): Show | 8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1165_369+1166d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATAT | 6 | a0001c0001t0002g0254a0002c0002t0001g0046a0002c0002t0001g0092others(3): Show | 6 | HG02965.hp1 NA18990.hp1 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1163_369+1166d others(6): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(1): Show |
4 | a0002c0002t0001g0036a0002c0002t0001g0072a0002c0002t0001g0096others(1): Show | 4 | HG02735.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1159_369+1166d others(10): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(3): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0148others(12): Show | 18 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.369+1157_369+1166d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(5): Show |
20 | a0001c0001t0001g0006a0001c0001t0001g0147a0001c0001t0001g0179others(17): Show | 23 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.369+1155_369+1166d others(14): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(7): Show |
25 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0153others(22): Show | 27 | HG00408.hp1 HG00544.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1153_369+1166d others(16): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(9): Show |
16 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0018others(13): Show | 21 | HG02071.hp1 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.369+1151_369+1166d others(18): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(11): Show |
8 | a0001c0001t0001g0185a0001c0001t0001g0211a0001c0001t0012g0249others(5): Show | 8 | HG01346.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1149_369+1166d others(20): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(13): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0205a0001c0001t0001g0255others(1): Show | 4 | HG04228.hp2 NA18986.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1147_369+1166d others(22): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(15): Show |
6 | a0001c0001t0001g0171a0001c0001t0001g0193a0002c0002t0001g0042others(3): Show | 6 | HG01261.hp1 HG02273.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1145_369+1166d others(24): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(17): Show |
3 | a0001c0001t0001g0192a0002c0002t0001g0104a0002c0002t0001g0116 | 3 | HG00741.hp1 HG01243.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(26): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(19): Show |
5 | a0001c0001t0001g0184a0002c0002t0001g0053a0002c0002t0001g0068others(2): Show | 5 | HG01074.hp2 HG02155.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1166_369+1167i others(28): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(21): Show |
1 | a0002c0002t0001g0085 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.369+1166_369+1167i others(30): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(23): Show |
4 | a0002c0002t0001g0041a0002c0002t0001g0052a0002c0002t0001g0057others(1): Show | 4 | HG00323.hp1 HG01891.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1166_369+1167i others(32): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(25): Show |
2 | a0001c0001t0001g0230a0001c0001t0001g0239 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(34): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(27): Show |
1 | a0002c0002t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.369+1166_369+1167i others(36): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(29): Show |
1 | a0002c0002t0001g0008 | 2 | HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.369+1166_369+1167i others(38): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633505
|
A | AATATATA others(31): Show |
1 | a0002c0002t0001g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.369+1166_369+1167i others(40): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633505 | ||||||
chr11:47633516
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.369+1140_369+1155d others(18): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633516 | ||||||
chr11:47633520
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.369+1141_369+1151d others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633520 | ||||||
chr11:47633522
|
ATATATTT others(3): Show |
A | 4 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | HG01168.hp2 HG01358.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1140_369+1149d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633522 | ||||||
chr11:47633524
|
ATATTTTT others(3): Show |
A | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.369+1138_369+1147d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633524 | ||||||
chr11:47633524
|
ATATTTTT others(4): Show |
A | 2 | a0001c0001t0001g0296a0001c0001t0001g0305 | 2 | NA18947.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.369+1137_369+1147d others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633524 | ||||||
chr11:47633526
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(23): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0021 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369+1145_369+1146i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0250 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(43): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(29): Show |
1 | a0002c0002t0001g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(38): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0234 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(39): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(27): Show |
1 | a0002c0002t0001g0051 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(36): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(24): Show |
1 | a0002c0002t0001g0049 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.369+1145_369+1146i others(28): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0228 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.369+1145_369+1146i others(26): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0001g0026a0001c0001t0001g0127a0001c0001t0001g0266others(4): Show | 8 | HG02004.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1137_369+1145d others(11): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633526
|
ATTTTTTT others(3): Show |
A | 9 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0128others(6): Show | 10 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.369+1136_369+1145d others(12): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633526 | ||||||
chr11:47633527
|
T | TATA | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0227others(4): Show | 7 | HG02132.hp2 HG02280.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(5): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(2): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0156a0001c0001t0001g0175others(2): Show | 6 | HG01099.hp1 HG01109.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(11): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(4): Show |
8 | a0001c0001t0001g0315a0001c0001t0002g0226a0001c0001t0003g0222others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(13): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(6): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0174a0001c0001t0001g0190others(3): Show | 7 | HG02148.hp2 HG02300.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(15): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(8): Show |
5 | a0001c0001t0001g0166a0001c0001t0001g0240a0001c0001t0001g0245others(2): Show | 6 | HG02258.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(17): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(10): Show |
4 | a0002c0002t0001g0032a0002c0002t0001g0067a0002c0002t0001g0083others(1): Show | 4 | HG00597.hp1 HG01358.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(19): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(12): Show |
6 | a0001c0001t0001g0161a0001c0001t0001g0183a0001c0001t0001g0196others(3): Show | 6 | HG02630.hp1 HG03041.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(21): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(14): Show |
5 | a0001c0001t0001g0182a0002c0002t0001g0038a0002c0002t0001g0065others(2): Show | 5 | HG00438.hp2 HG02809.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(23): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(16): Show |
2 | a0001c0001t0003g0218a0001c0001t0003g0220 | 2 | HG01257.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(25): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(18): Show |
3 | a0002c0002t0001g0045a0002c0002t0001g0082a0002c0002t0001g0114 | 3 | HG00735.hp2 HG01192.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(27): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(20): Show |
1 | a0002c0002t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.369+1144_369+1145i others(29): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(22): Show |
3 | a0002c0002t0001g0040a0002c0002t0001g0063a0002c0002t0001g0103 | 3 | HG01515.hp1 HG03654.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(31): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(24): Show |
6 | a0001c0001t0003g0219a0002c0002t0001g0034a0002c0002t0001g0055others(3): Show | 6 | HG01071.hp1 HG01074.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(33): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(26): Show |
5 | a0001c0001t0001g0237a0002c0002t0001g0078a0002c0002t0001g0079others(2): Show | 5 | HG03239.hp2 HG03540.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1144_369+1145i others(35): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(28): Show |
2 | a0002c0002t0001g0033a0002c0002t0001g0077 | 2 | NA18981.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.369+1144_369+1145i others(37): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(30): Show |
1 | a0002c0002t0001g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.369+1144_369+1145i others(39): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATATATA others(32): Show |
1 | a0002c0002t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.369+1144_369+1145i others(41): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633527
|
T | TATTATAT others(11): Show |
1 | a0001c0001t0001g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.369+1144_369+1145i others(20): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633527 | ||||||
chr11:47633528
|
T | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.369+1144A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633528 | ||||||
chr11:47633529
|
T | A | 67 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0150others(64): Show | 70 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.369+1143A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633529 | ||||||
chr11:47633530
|
T | A | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 118 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.369+1142A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633530 | ||||||
chr11:47633531
|
T | A | 46 | a0001c0001t0001g0013a0001c0001t0001g0161a0001c0001t0001g0182others(43): Show | 47 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.369+1141A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633531 | ||||||
chr11:47633532
|
T | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0018others(62): Show | 74 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.369+1140A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633532 | ||||||
chr11:47633533
|
T | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0161a0001c0001t0001g0190others(18): Show | 22 | HG00438.hp2 HG01109.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.369+1139A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633533 | ||||||
chr11:47633534
|
T | A | 21 | a0001c0001t0001g0163a0001c0001t0001g0200a0001c0001t0001g0210others(18): Show | 23 | HG00408.hp1 HG01074.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.369+1138A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633534 | ||||||
chr11:47633535
|
T | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 6 | HG02132.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1137A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633535 | ||||||
chr11:47633536
|
T | A | 4 | a0001c0001t0001g0265a0002c0002t0001g0098a0002c0002t0001g0115others(1): Show | 4 | NA18942.hp2 NA18956.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1136A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633536 | ||||||
chr11:47633537
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.369+1135A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633537 | ||||||
chr11:47633538
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.369+1134A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633538 | ||||||
chr11:47633779
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.369+893G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633779 | ||||||
chr11:47633828
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(82): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.369+844G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633828 | ||||||
chr11:47633833
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.369+839T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47633833 | ||||||
chr11:47634103
|
T | C | 1 | a0002c0002t0001g0099 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.369+569A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634103 | ||||||
chr11:47634200
|
C | T | 87 | a0002c0002t0001g0008a0002c0002t0001g0032a0002c0002t0001g0033others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.369+472G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634200 | ||||||
chr11:47634322
|
T | G | 2 | a0002c0002t0001g0036a0002c0002t0001g0111 | 2 | HG02735.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.369+350A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634322 | ||||||
chr11:47634390
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.369+282G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634390 | ||||||
chr11:47634443
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+229G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 5/12 | chr11 | 47634443 | ||||||
chr11:47634769
|
A | AT | 43 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 49 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.307-36dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | ||||||
chr11:47634769
|
A | ATT | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(52): Show | 74 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.307-37_307-36dupAA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | ||||||
chr11:47634769
|
A | ATTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0272others(5): Show | 16 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.307-38_307-36dupAA others(1): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | ||||||
chr11:47634769
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.307-45_307-36delAA others(8): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634769 | ||||||
chr11:47634808
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.307-74A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634808 | ||||||
chr11:47634842
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-108C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634842 | ||||||
chr11:47634962
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.307-228C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634962 | ||||||
chr11:47634993
|
G | C | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-259C>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47634993 | ||||||
chr11:47635067
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.307-333C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635067 | ||||||
chr11:47635098
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.307-364C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635098 | ||||||
chr11:47635111
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.307-377C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635111 | ||||||
chr11:47635374
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+171G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635374 | ||||||
chr11:47635421
|
T | C | 2 | a0001c0001t0005g0136a0001c0001t0005g0137 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.306+124A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 4/12 | chr11 | 47635421 | ||||||
chr11:47635684
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.280-113A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635684 | ||||||
chr11:47635739
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-168T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635739 | ||||||
chr11:47635795
|
T | C | 1 | a0001c0001t0005g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.280-224A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635795 | ||||||
chr11:47635838
|
A | G | 1 | a0002c0002t0001g0037 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280-267T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635838 | ||||||
chr11:47635845
|
G | A | 17 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0023others(14): Show | 20 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.280-274C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635845 | ||||||
chr11:47635984
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-413C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47635984 | ||||||
chr11:47636128
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.280-557T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636128 | ||||||
chr11:47636519
|
G | A | 1 | a0002c0002t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.280-948C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636519 | ||||||
chr11:47636593
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0224a0001c0001t0002g0225others(1): Show | 5 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1022C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636593 | ||||||
chr11:47636622
|
C | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0147others(24): Show | 30 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.280-1051G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636622 | ||||||
chr11:47636623
|
G | A | 13 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0023others(10): Show | 16 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-1052C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636623 | ||||||
chr11:47636741
|
A | C | 1 | a0001c0001t0006g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-1170T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636741 | ||||||
chr11:47636762
|
C | T | 87 | a0002c0002t0001g0008a0002c0002t0001g0032a0002c0002t0001g0033others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.280-1191G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636762 | ||||||
chr11:47636790
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280-1219C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636790 | ||||||
chr11:47636931
|
C | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0200others(6): Show | 10 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.280-1360G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636931 | ||||||
chr11:47636951
|
C | G | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1380G>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636951 | ||||||
chr11:47636961
|
G | GT | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.280-1391dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636961 | ||||||
chr11:47636961
|
G | GTT | 12 | a0001c0001t0001g0122a0001c0001t0001g0149a0001c0001t0001g0167others(9): Show | 12 | HG00741.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.280-1392_280-1391d others(4): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47636961 | ||||||
chr11:47637019
|
GCAATCTC others(25): Show |
G | 1 | a0002c0002t0001g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-1480_280-1449d others(34): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637019 | ||||||
chr11:47637452
|
G | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 8 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+1247C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637452 | ||||||
chr11:47637499
|
G | GT | 6 | a0001c0001t0001g0166a0001c0001t0001g0232a0001c0001t0001g0280others(3): Show | 6 | HG03041.hp2 HG03831.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1199dupA | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637499 | ||||||
chr11:47637578
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+1121C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637578 | ||||||
chr11:47637579
|
T | G | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+1120A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637579 | ||||||
chr11:47637583
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0024others(41): Show | 67 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+1116C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637583 | ||||||
chr11:47637890
|
T | G | 1 | a0002c0002t0001g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.279+809A>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47637890 | ||||||
chr11:47638129
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.279+570A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638129 | ||||||
chr11:47638333
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.279+366C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638333 | ||||||
chr11:47638360
|
G | GAACACGG others(4543): Show |
1 | a0001c0001t0001g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0205 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0012g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG02257.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0206 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0259 | 3 | HG01071.hp2 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4539): Show |
1 | a0001c0001t0001g0257 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0004c0005t0001g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4543): Show |
5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00408.hp1 HG02486.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0214 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0231 | 2 | HG03041.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4543): Show |
1 | a0001c0001t0001g0240 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 78 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4538): Show |
1 | a0001c0001t0001g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4545): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0149a0001c0001t0001g0154others(3): Show | 7 | HG02280.hp1 HG03130.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
6 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0006g0143others(3): Show | 6 | HG02071.hp2 HG02523.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4539): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0303a0001c0001t0013g0302 | 3 | HG01168.hp2 HG02145.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA19005.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0306 | 2 | HG01175.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0258 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0260 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4539): Show |
2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00639.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4549): Show |
1 | a0001c0001t0005g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4556): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4547): Show |
1 | a0001c0001t0005g0136 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4554): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | NA18942.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0267 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0131 | 3 | HG02965.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0003c0004t0001g0268 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
4 | a0001c0001t0002g0020a0001c0001t0002g0224a0001c0001t0002g0225others(1): Show | 5 | HG02723.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
6 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0001c0001t0011g0314 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
8 | a0001c0001t0001g0021a0001c0001t0001g0233a0001c0001t0001g0234others(5): Show | 9 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0001c0001t0001g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0001c0001t0001g0163 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0246others(5): Show | 10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4538): Show |
2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4545): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0164a0001c0001t0001g0165 | 4 | NA18945.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0103 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0105 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0002c0002t0001g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
2 | a0002c0002t0001g0106a0002c0002t0001g0115 | 2 | NA18956.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
2 | a0002c0002t0001g0108a0002c0002t0001g0109 | 2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
1 | a0002c0002t0001g0112 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
68 | a0002c0002t0001g0008a0002c0002t0001g0032a0002c0002t0001g0033others(65): Show | 69 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
3 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041 | 3 | HG00323.hp1 NA18994.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0042 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4539): Show |
1 | a0002c0002t0001g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4546): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0002c0002t0001g0043 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4542): Show |
1 | a0002c0002t0001g0044 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4549): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4543): Show |
1 | a0002c0002t0001g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4550): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4541): Show |
1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+338_279+339ins others(4548): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638360
|
G | GAACACGG others(4540): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0120a0005c0003t0001g0118 | 3 | HG01243.hp1 HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.279+338_279+339ins others(4547): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638360 | ||||||
chr11:47638367
|
G | GTGAAACC others(4519): Show |
1 | a0002c0002t0001g0037 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.279+331_279+332ins others(4526): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638367 | ||||||
chr11:47638376
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.279+323A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638376 | ||||||
chr11:47638386
|
A | AAAAATAC others(4532): Show |
1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.279+312_279+313ins others(4539): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638386 | ||||||
chr11:47638449
|
G | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(82): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.279+250C>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638449 | ||||||
chr11:47638488
|
G | A | 1 | a0002c0002t0009g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.279+211C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638488 | ||||||
chr11:47638491
|
A | G | 1 | a0002c0002t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.279+208T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638491 | ||||||
chr11:47638503
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.279+196C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638503 | ||||||
chr11:47638545
|
C | CA | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.279+153dupT | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638545 | ||||||
chr11:47638545
|
C | CAA | 22 | a0001c0001t0001g0133a0001c0001t0001g0242a0001c0001t0001g0243others(19): Show | 24 | HG00544.hp1 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+152_279+153dup others(2): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 3/12 | chr11 | 47638545 | ||||||
chr11:47639331
|
G | A | 3 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02630.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.88-280C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639331 | ||||||
chr11:47639500
|
A | C | 1 | a0001c0001t0001g0152 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88-449T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639500 | ||||||
chr11:47639556
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.88-505C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639556 | ||||||
chr11:47639762
|
C | T | 1 | a0002c0002t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88-711G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639762 | ||||||
chr11:47639803
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.88-752T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639803 | ||||||
chr11:47639867
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88-816T>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639867 | ||||||
chr11:47639936
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88-885C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639936 | ||||||
chr11:47639946
|
C | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 24 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-895G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639946 | ||||||
chr11:47639989
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88-938C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47639989 | ||||||
chr11:47640064
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88-1013G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640064 | ||||||
chr11:47640203
|
C | A | 1 | a0001c0001t0006g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.88-1152G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640203 | ||||||
chr11:47640203
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88-1152G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640203 | ||||||
chr11:47640223
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.88-1172T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640223 | ||||||
chr11:47640446
|
C | T | 4 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-1395G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640446 | ||||||
chr11:47640556
|
C | T | 7 | a0001c0001t0004g0012a0001c0001t0004g0139a0001c0001t0004g0142others(4): Show | 8 | HG02647.hp2 HG02809.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.88-1505G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640556 | ||||||
chr11:47640580
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.88-1529A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640580 | ||||||
chr11:47640681
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.88-1630C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640681 | ||||||
chr11:47640785
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.87+1594A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640785 | ||||||
chr11:47640806
|
T | TAAGAATA others(284): Show |
1 | a0001c0001t0001g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(291): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | ||||||
chr11:47640806
|
T | TAAGAATA others(285): Show |
1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(292): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | ||||||
chr11:47640806
|
T | TAAGAATA others(286): Show |
1 | a0001c0001t0001g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.87+1572_87+1573ins others(293): Show |
MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640806 | ||||||
chr11:47640956
|
G | A | 1 | a0002c0002t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.87+1423C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47640956 | ||||||
chr11:47641037
|
C | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 27 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.87+1342G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641037 | ||||||
chr11:47641226
|
C | T | 5 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0316others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+1153G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641226 | ||||||
chr11:47641380
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.87+999A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641380 | ||||||
chr11:47641497
|
A | G | 87 | a0002c0002t0001g0008a0002c0002t0001g0032a0002c0002t0001g0033others(84): Show | 88 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.87+882T>C | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641497 | ||||||
chr11:47641558
|
T | C | 1 | a0001c0001t0004g0311 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.87+821A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641558 | ||||||
chr11:47641596
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.87+783A>G | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641596 | ||||||
chr11:47641793
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.87+586A>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641793 | ||||||
chr11:47641794
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.87+585G>A | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47641794 | ||||||
chr11:47642090
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.87+289G>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47642090 | ||||||
chr11:47642340
|
G | A | 5 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0316others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+39C>T | MTCH2 | ENSG00000109919.10 | transcript | ENST00000302503.8 | protein_coding | 1/12 | chr11 | 47642340 |