geneid | 7047 |
---|---|
ensemblid | ENSG00000163810.13 |
hgncid | 11780 |
symbol | TGM4 |
name | transglutaminase 4 |
refseq_nuc | NM_003241.4 |
refseq_prot | NP_003232.2 |
ensembl_nuc | ENST00000296125.9 |
ensembl_prot | ENSP00000296125.4 |
mane_status | MANE Select |
chr | chr3 |
start | 44874608 |
end | 44914990 |
strand | + |
ver | v1.2 |
region | chr3:44874608-44914990 |
region5000 | chr3:44869608-44919990 |
regionname0 | TGM4_chr3_44874608_44914990 |
regionname5000 | TGM4_chr3_44869608_44919990 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 684 | 86 | 9 | 18 | 43 | 2 | 14 | 27 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002 | 1/1 | 684 | 84 | 18 | 28 | 20 | 7 | 9 | 16 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0003 | 0/0 | 684 | 36 | 10 | 5 | 9 | 1 | 11 | 5 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0004 | 0/0 | 684 | 31 | 4 | 13 | 8 | 4 | 2 | 7 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0005 | 0/0 | 684 | 15 | 12 | 2 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006 | 0/0 | 684 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0007 | 0/0 | 684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0008 | 0/0 | 684 | 7 | 4 | 2 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0009 | 0/0 | 684 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0010 | 0/0 | 684 | 6 | 5 | 0 | 1 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0011 | 0/0 | 684 | 5 | 4 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0012 | 0/0 | 684 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0013 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0014 | 0/0 | 684 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0015 | 0/0 | 684 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0016 | 0/0 | 684 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0017 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0018 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0019 | 0/0 | 268 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0020 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0021 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0022 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0023 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0024 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0025 | 0/0 | 268 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0026 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0027 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2055 | 83 | 9 | 18 | 40 | 2 | 14 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0002 | 1/1 | 2055 | 79 | 15 | 26 | 20 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0003 | 0/0 | 2055 | 36 | 10 | 5 | 9 | 1 | 11 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0004 | 0/0 | 2055 | 30 | 4 | 13 | 7 | 4 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0005 | 0/0 | 2055 | 15 | 12 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0006 | 0/0 | 2055 | 7 | 7 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0007 | 0/0 | 2055 | 7 | 4 | 2 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0008 | 0/0 | 2055 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0009 | 0/0 | 2055 | 6 | 5 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0010 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0011 | 0/0 | 2055 | 5 | 4 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0012 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0013 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0014 | 0/0 | 2055 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0015 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0016 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0017 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0018 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0019 | 0/0 | 2055 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0020 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0021 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0022 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0023 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0024 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0025 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0026 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0027 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0028 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0029 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0030 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0031 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
c0032 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1337 | 184 | 52 | 34 | 62 | 9 | 27 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0002 | 1/1 | 1337 | 83 | 14 | 30 | 21 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0003 | 0/0 | 1337 | 14 | 14 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0004 | 0/0 | 1337 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0005 | 0/0 | 1337 | 5 | 4 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0006 | 0/0 | 1337 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0007 | 0/0 | 1337 | 4 | 0 | 4 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0008 | 0/0 | 1337 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0009 | 0/0 | 1337 | 3 | 0 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0010 | 0/0 | 1337 | 3 | 2 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0011 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0012 | 0/0 | 618 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0013 | 0/0 | 1337 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0014 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
t0015 | 0/0 | 1337 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0279 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2055 | 83 | 9 | 18 | 40 | 2 | 14 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0001c0014 | 0/0 | 2055 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0002 | 1/1 | 2055 | 79 | 15 | 26 | 20 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0013 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0018 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0003c0003 | 0/0 | 2055 | 36 | 10 | 5 | 9 | 1 | 11 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0004c0004 | 0/0 | 2055 | 30 | 4 | 13 | 7 | 4 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0004c0023 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0005c0005 | 0/0 | 2055 | 15 | 12 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006c0010 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006c0015 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0007c0006 | 0/0 | 2055 | 7 | 7 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0008c0007 | 0/0 | 2055 | 7 | 4 | 2 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0009c0008 | 0/0 | 2055 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0010c0009 | 0/0 | 2055 | 6 | 5 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0011c0011 | 0/0 | 2055 | 5 | 4 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0012c0012 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0013c0017 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0014c0016 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0015c0019 | 0/0 | 2055 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0016c0020 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0017c0024 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0018c0025 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0019c0022 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0020c0021 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0021c0030 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0022c0026 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0023c0027 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0024c0028 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0025c0029 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0026c0031 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0027c0032 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3391 | 80 | 9 | 16 | 40 | 2 | 13 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0001c0001t0007 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0001c0001t0013 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0001c0001t0015 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0001c0014t0001 | 0/0 | 3391 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0002t0002 | 1/1 | 3391 | 76 | 13 | 25 | 20 | 7 | 9 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0002t0010 | 0/0 | 3391 | 3 | 2 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0013t0006 | 0/0 | 3391 | 3 | 3 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0002c0018t0002 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0003c0003t0001 | 0/0 | 3391 | 32 | 10 | 2 | 8 | 1 | 11 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0003c0003t0007 | 0/0 | 3391 | 3 | 0 | 3 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0003c0003t0014 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0004c0004t0001 | 0/0 | 3391 | 30 | 4 | 13 | 7 | 4 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0004c0023t0001 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0005c0005t0001 | 0/0 | 3391 | 12 | 12 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0005c0005t0009 | 0/0 | 3391 | 3 | 0 | 2 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006c0010t0003 | 0/0 | 3391 | 5 | 5 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006c0015t0003 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0006c0015t0008 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0007c0006t0003 | 0/0 | 3391 | 7 | 7 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0008c0007t0001 | 0/0 | 3391 | 6 | 3 | 2 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0008c0007t0012 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0009c0008t0004 | 0/0 | 3391 | 6 | 0 | 0 | 6 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0010c0009t0005 | 0/0 | 3391 | 5 | 4 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0010c0009t0008 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0011c0011t0001 | 0/0 | 3391 | 5 | 4 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0012c0012t0001 | 0/0 | 3391 | 4 | 4 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0013c0017t0001 | 0/0 | 3391 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0014c0016t0002 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0015c0019t0002 | 0/0 | 3391 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0016c0020t0001 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0017c0024t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0018c0025t0011 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0019c0022t0001 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0020c0021t0001 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0021c0030t0003 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0022c0026t0006 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0023c0027t0002 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0024c0028t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0025c0029t0001 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0026c0031t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
a0027c0032t0001 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | copy fasta | chr3 | 44869608 | 44919990 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0013g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0001t0015g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0014t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0001c0014t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0279 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0010g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0002t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0013t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0002c0018t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0003c0003t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0004c0023t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0005c0005t0009g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0010t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0006c0015t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0007c0006t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0008c0007t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0009c0008t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0010c0009t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0011c0011t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0012t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0012t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0012t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0012c0012t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0013c0017t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0013c0017t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0014c0016t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0014c0016t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0015c0019t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0015c0019t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0016c0020t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0016c0020t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0017c0024t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0018c0025t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0019c0022t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0020c0021t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0021c0030t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0022c0026t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0023c0027t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0024c0028t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0025c0029t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0026c0031t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
a0027c0032t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0008 | c0007 | t0001 | g0055 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0235 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0284 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0107 | EUR | GBR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0275 | EUR | FIN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0114 | EUR | FIN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00639 | hp1 | a0004 | c0004 | t0001 | g0126 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0146 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00642 | hp2 | a0005 | c0005 | t0009 | g0032 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00673 | hp2 | a0020 | c0021 | t0001 | g0254 | EAS | CHS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0082 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00741 | hp1 | a0008 | c0007 | t0001 | g0210 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG00741 | hp2 | a0015 | c0019 | t0002 | g0127 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0236 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01071 | hp1 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01074 | hp2 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0239 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01099 | hp2 | a0004 | c0004 | t0001 | g0237 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01106 | hp1 | a0004 | c0004 | t0001 | g0147 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01109 | hp2 | a0008 | c0007 | t0001 | g0034 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01167 | hp1 | a0019 | c0022 | t0001 | g0244 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01167 | hp2 | a0002 | c0018 | t0002 | g0002 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01169 | hp2 | a0002 | c0018 | t0002 | g0002 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01192 | hp2 | a0005 | c0005 | t0009 | g0135 | AMR | PUR | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01255 | hp1 | a0014 | c0016 | t0002 | g0257 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0106 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01256 | hp2 | a0004 | c0004 | t0001 | g0148 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0269 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0111 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0084 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01496 | hp2 | a0003 | c0003 | t0007 | g0043 | AMR | CLM | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0270 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01515 | hp2 | a0004 | c0004 | t0001 | g0238 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0145 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01517 | hp2 | a0004 | c0004 | t0001 | g0241 | EUR | IBS | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01884 | hp2 | a0007 | c0006 | t0003 | g0009 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01891 | hp1 | a0012 | c0012 | t0001 | g0117 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0138 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0044 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01943 | hp2 | a0004 | c0004 | t0001 | g0258 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01975 | hp1 | a0014 | c0016 | t0002 | g0051 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01978 | hp1 | a0001 | c0001 | t0015 | g0014 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG01993 | hp2 | a0004 | c0004 | t0001 | g0259 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02055 | hp2 | a0024 | c0028 | t0001 | g0116 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02056 | hp2 | a0018 | c0025 | t0011 | g0181 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02071 | hp1 | a0001 | c0014 | t0001 | g0226 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02074 | hp2 | a0003 | c0003 | t0014 | g0054 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02129 | hp1 | a0001 | c0014 | t0001 | g0015 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02135 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02145 | hp1 | a0015 | c0019 | t0002 | g0131 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0007 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02148 | hp1 | a0004 | c0004 | t0001 | g0260 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02257 | hp1 | a0007 | c0006 | t0003 | g0038 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02258 | hp1 | a0005 | c0005 | t0001 | g0119 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02258 | hp2 | a0010 | c0009 | t0008 | g0262 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02273 | hp1 | a0004 | c0004 | t0001 | g0255 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02273 | hp2 | a0003 | c0003 | t0007 | g0046 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0079 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02280 | hp2 | a0012 | c0012 | t0001 | g0118 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0173 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02300 | hp1 | a0002 | c0002 | t0010 | g0283 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02300 | hp2 | a0003 | c0003 | t0007 | g0093 | AMR | PEL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02523 | hp1 | a0004 | c0023 | t0001 | g0245 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02572 | hp1 | a0017 | c0024 | t0001 | g0186 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02572 | hp2 | a0004 | c0004 | t0001 | g0292 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02602 | hp1 | a0004 | c0004 | t0001 | g0224 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0198 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0122 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02615 | hp2 | a0004 | c0004 | t0001 | g0264 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02622 | hp1 | a0008 | c0007 | t0001 | g0033 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02622 | hp2 | a0005 | c0005 | t0001 | g0088 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02630 | hp1 | a0002 | c0013 | t0006 | g0158 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0277 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0144 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0282 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0042 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02717 | hp2 | a0002 | c0013 | t0006 | g0156 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0103 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02723 | hp2 | a0007 | c0006 | t0003 | g0039 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02809 | hp1 | a0011 | c0011 | t0001 | g0025 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02809 | hp2 | a0005 | c0005 | t0001 | g0010 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02818 | hp1 | a0006 | c0015 | t0008 | g0124 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02818 | hp2 | a0021 | c0030 | t0003 | g0268 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02886 | hp1 | a0007 | c0006 | t0003 | g0289 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02895 | hp1 | a0005 | c0005 | t0001 | g0129 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02895 | hp2 | a0011 | c0011 | t0001 | g0027 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02896 | hp1 | a0011 | c0011 | t0001 | g0026 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02896 | hp2 | a0002 | c0002 | t0010 | g0018 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0018 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0128 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02922 | hp1 | a0012 | c0012 | t0001 | g0115 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02922 | hp2 | a0016 | c0020 | t0001 | g0030 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02965 | hp2 | a0011 | c0011 | t0001 | g0028 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02970 | hp1 | a0005 | c0005 | t0001 | g0007 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02976 | hp2 | a0010 | c0009 | t0005 | g0153 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0049 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0137 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03041 | hp2 | a0007 | c0006 | t0003 | g0040 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0287 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03098 | hp2 | a0006 | c0010 | t0003 | g0058 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0285 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03130 | hp2 | a0027 | c0032 | t0001 | g0024 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03139 | hp1 | a0010 | c0009 | t0005 | g0267 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03139 | hp2 | a0007 | c0006 | t0003 | g0009 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0276 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03209 | hp2 | a0008 | c0007 | t0001 | g0100 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0278 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0291 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03453 | hp1 | a0010 | c0009 | t0005 | g0266 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03486 | hp1 | a0007 | c0006 | t0003 | g0041 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03486 | hp2 | a0006 | c0015 | t0003 | g0133 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0290 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03516 | hp1 | a0005 | c0005 | t0001 | g0101 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03516 | hp2 | a0006 | c0010 | t0003 | g0053 | AFR | ESN | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03540 | hp2 | a0006 | c0015 | t0008 | g0123 | AFR | GWD | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0069 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0104 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03669 | hp1 | a0005 | c0005 | t0009 | g0125 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03669 | hp2 | a0004 | c0004 | t0001 | g0175 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0286 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0110 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0056 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0047 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0066 | SAS | BEB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0060 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18522 | hp2 | a0010 | c0009 | t0005 | g0265 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18612 | hp1 | a0013 | c0017 | t0001 | g0166 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0293 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0140 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18942 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0222 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18964 | hp2 | a0004 | c0004 | t0001 | g0246 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18970 | hp1 | a0010 | c0009 | t0005 | g0263 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18975 | hp1 | a0009 | c0008 | t0004 | g0179 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18977 | hp1 | a0013 | c0017 | t0001 | g0178 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18981 | hp1 | a0004 | c0004 | t0001 | g0242 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18984 | hp1 | a0009 | c0008 | t0004 | g0165 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18991 | hp1 | a0009 | c0008 | t0004 | g0157 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA18998 | hp2 | a0009 | c0008 | t0004 | g0249 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19003 | hp1 | a0009 | c0008 | t0004 | g0194 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0280 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19030 | hp2 | a0008 | c0007 | t0001 | g0074 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19043 | hp1 | a0008 | c0007 | t0012 | g0136 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0072 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19056 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19063 | hp2 | a0001 | c0014 | t0001 | g0015 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19065 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19068 | hp2 | a0009 | c0008 | t0004 | g0253 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19077 | hp1 | a0023 | c0027 | t0002 | g0090 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19077 | hp2 | a0004 | c0004 | t0001 | g0261 | EAS | JPT | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA19240 | hp2 | a0005 | c0005 | t0001 | g0102 | AFR | YRI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20129 | hp1 | a0016 | c0020 | t0001 | g0029 | AFR | ASW | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0099 | AFR | ASW | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0086 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0061 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20805 | hp1 | a0011 | c0011 | t0001 | g0023 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0105 | EUR | TSI | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20905 | hp2 | a0025 | c0029 | t0001 | g0121 | SAS | GIH | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02109 | hp2 | a0005 | c0005 | t0001 | g0010 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02486 | hp1 | a0002 | c0013 | t0006 | g0168 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02486 | hp2 | a0004 | c0004 | t0001 | g0243 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG02559 | hp2 | a0006 | c0010 | t0003 | g0037 | AFR | ACB | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG03471 | hp2 | a0012 | c0012 | t0001 | g0083 | AFR | MSL | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0272 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
HG06807 | hp2 | a0006 | c0010 | t0003 | g0006 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20300 | hp1 | a0006 | c0010 | t0003 | g0006 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA20300 | hp2 | a0005 | c0005 | t0001 | g0132 | AFR | USA | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA21309 | hp1 | a0022 | c0026 | t0006 | g0229 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
NA21309 | hp2 | a0026 | c0031 | t0001 | g0031 | AFR | LWK | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0036 | REF | REF | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0279 | REF | REF | TGM4_chr3_44869608_44919990 | TGM4 | chr3 | 44869608 | 44919990 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44887795
|
G | C | 9 | a0001a0004a0009others(6): Show | 131 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(128): Show |
missense_variant&splice_region_variant | MODERATE | c.300G>C | p.Glu100Asp | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/14 | 371/3391 | 300/2055 | 100/684 | chr3 | 44887795 | ||
chr3:44893589
|
T | C | 1 | a0020 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.443T>C | p.Phe148Ser | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 514/3391 | 443/2055 | 148/684 | chr3 | 44893589 | ||
chr3:44893613
|
A | G | 4 | a0011a0016a0026others(1): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
missense_variant | MODERATE | c.467A>G | p.Lys156Arg | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 538/3391 | 467/2055 | 156/684 | chr3 | 44893613 | ||
chr3:44896799
|
A | G | 1 | a0021 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.640A>G | p.Arg214Gly | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/14 | 711/3391 | 640/2055 | 214/684 | chr3 | 44896799 | ||
chr3:44901596
|
T | C | 5 | a0006a0007a0010others(2): Show | 23 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(20): Show |
missense_variant | MODERATE | c.730T>C | p.Tyr244His | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 801/3391 | 730/2055 | 244/684 | chr3 | 44901596 | ||
chr3:44901612
|
G | C | 3 | a0004a0019a0025 | 33 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
missense_variant | MODERATE | c.746G>C | p.Ser249Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 817/3391 | 746/2055 | 249/684 | chr3 | 44901612 | ||
chr3:44901672
|
G | A | 2 | a0019a0025 | 2 | HG01167.hp1 NA20905.hp2 |
stop_gained | HIGH | c.806G>A | p.Trp269* | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 877/3391 | 806/2055 | 269/684 | chr3 | 44901672 | ||
chr3:44901897
|
G | A | 15 | a0001a0004a0005others(12): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
missense_variant | MODERATE | c.937G>A | p.Glu313Lys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/14 | 1008/3391 | 937/2055 | 313/684 | chr3 | 44901897 | ||
chr3:44901907
|
C | A | 1 | a0009 | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
missense_variant | MODERATE | c.947C>A | p.Thr316Asn | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/14 | 1018/3391 | 947/2055 | 316/684 | chr3 | 44901907 | ||
chr3:44903951
|
C | A | 1 | a0022 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1039C>A | p.Gln347Lys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/14 | 1110/3391 | 1039/2055 | 347/684 | chr3 | 44903951 | ||
chr3:44906987
|
C | T | 19 | a0001a0003a0004others(16): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
missense_variant | MODERATE | c.1114C>T | p.Arg372Cys | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1185/3391 | 1114/2055 | 372/684 | chr3 | 44906987 | ||
chr3:44906988
|
G | A | 1 | a0012 | 4 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1115G>A | p.Arg372His | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1186/3391 | 1115/2055 | 372/684 | chr3 | 44906988 | ||
chr3:44906999
|
A | G | 2 | a0011a0024 | 6 | HG02055.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.1126A>G | p.Ile376Val | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1197/3391 | 1126/2055 | 376/684 | chr3 | 44906999 | ||
chr3:44907026
|
G | A | 2 | a0009a0023 | 7 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(4): Show |
missense_variant | MODERATE | c.1153G>A | p.Val385Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1224/3391 | 1153/2055 | 385/684 | chr3 | 44907026 | ||
chr3:44907098
|
G | A | 14 | a0001a0003a0004others(11): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
missense_variant | MODERATE | c.1225G>A | p.Val409Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1296/3391 | 1225/2055 | 409/684 | chr3 | 44907098 | ||
chr3:44907125
|
G | A | 1 | a0017 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1252G>A | p.Gly418Arg | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1323/3391 | 1252/2055 | 418/684 | chr3 | 44907125 | ||
chr3:44907182
|
G | C | 2 | a0005a0026 | 16 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(13): Show |
missense_variant | MODERATE | c.1309G>C | p.Glu437Gln | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1380/3391 | 1309/2055 | 437/684 | chr3 | 44907182 | ||
chr3:44913586
|
C | T | 1 | a0007 | 7 | HG01884.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.1916C>T | p.Thr639Met | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1987/3391 | 1916/2055 | 639/684 | chr3 | 44913586 | ||
chr3:44914271
|
CAGTTTGA others(1426): Show |
C | 1 | a0008 | 1 | NA19043.hp1 | splice_region_variant | LOW | c.*547_*1979del | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | chr3 | 44914271 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44885368
|
C | T | 1 | a0006c0015 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.63C>T | p.Ala21Ala | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/14 | 134/3391 | 63/2055 | 21/684 | chr3 | 44885368 | ||
chr3:44887747
|
A | G | 1 | a0001c0014 | 3 | HG02071.hp1 HG02129.hp1 NA19063.hp2 |
synonymous_variant | LOW | c.252A>G | p.Ser84Ser | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/14 | 323/3391 | 252/2055 | 84/684 | chr3 | 44887747 | ||
chr3:44893617
|
G | A | 4 | a0011c0011a0016c0020a0026c0031others(1): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
synonymous_variant | LOW | c.471G>A | p.Glu157Glu | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/14 | 542/3391 | 471/2055 | 157/684 | chr3 | 44893617 | ||
chr3:44901577
|
C | T | 19 | a0001c0001a0001c0014a0004c0004others(16): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
synonymous_variant | LOW | c.711C>T | p.Tyr237Tyr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 782/3391 | 711/2055 | 237/684 | chr3 | 44901577 | ||
chr3:44901637
|
C | T | 1 | a0026c0031 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.771C>T | p.Tyr257Tyr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 7/14 | 842/3391 | 771/2055 | 257/684 | chr3 | 44901637 | ||
chr3:44907055
|
C | T | 1 | a0006c0010 | 5 | HG02559.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
synonymous_variant | LOW | c.1182C>T | p.Leu394Leu | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1253/3391 | 1182/2055 | 394/684 | chr3 | 44907055 | ||
chr3:44907115
|
C | A | 1 | a0026c0031 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1242C>A | p.Thr414Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1313/3391 | 1242/2055 | 414/684 | chr3 | 44907115 | ||
chr3:44907124
|
C | T | 1 | a0002c0018 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1251C>T | p.Ile417Ile | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/14 | 1322/3391 | 1251/2055 | 417/684 | chr3 | 44907124 | ||
chr3:44910178
|
T | C | 1 | a0004c0023 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1416T>C | p.Phe472Phe | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/14 | 1487/3391 | 1416/2055 | 472/684 | chr3 | 44910178 | ||
chr3:44913719
|
C | T | 1 | a0002c0013 | 3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.2049C>T | p.Thr683Thr | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 2120/3391 | 2049/2055 | 683/684 | chr3 | 44913719 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44913726
|
C | G | 1 | a0002c0002t0010 | 3 | HG02300.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1 | chr3 | 44913726 | |||||
chr3:44913912
|
G | A | 8 | a0006c0010t0003a0006c0015t0003a0006c0015t0008others(5): Show | 23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 187 | chr3 | 44913912 | |||||
chr3:44913943
|
G | A | 2 | a0006c0015t0008a0010c0009t0008 | 3 | HG02258.hp2 HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*218G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 218 | chr3 | 44913943 | |||||
chr3:44914001
|
T | A | 1 | a0005c0005t0009 | 3 | HG00642.hp2 HG01192.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*276T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 276 | chr3 | 44914001 | |||||
chr3:44914038
|
G | T | 36 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(33): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 313 | chr3 | 44914038 | |||||
chr3:44914090
|
C | T | 1 | a0009c0008t0004 | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*365C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 365 | chr3 | 44914090 | |||||
chr3:44914353
|
C | T | 1 | a0001c0001t0015 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 628 | chr3 | 44914353 | |||||
chr3:44914406
|
A | G | 1 | a0003c0003t0014 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 681 | chr3 | 44914406 | |||||
chr3:44914486
|
T | C | 2 | a0002c0013t0006a0022c0026t0006 | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 761 | chr3 | 44914486 | |||||
chr3:44914606
|
G | C | 2 | a0010c0009t0005a0018c0025t0011 | 6 | HG02056.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*881G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 881 | chr3 | 44914606 | |||||
chr3:44914678
|
G | C | 1 | a0001c0001t0013 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 953 | chr3 | 44914678 | |||||
chr3:44914748
|
A | G | 3 | a0001c0001t0007a0003c0003t0007a0018c0025t0011 | 5 | HG01496.hp2 HG02056.hp2 HG02273.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1023A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 14/14 | 1023 | chr3 | 44914748 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44874719
|
G | A | 1 | a0002c0018t0002g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.19+22G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874719 | ||||||
chr3:44874741
|
C | A | 2 | a0002c0002t0002g0021a0002c0002t0002g0022 | 2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.19+44C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874741 | ||||||
chr3:44874907
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+210G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44874907 | ||||||
chr3:44875099
|
G | A | 263 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(260): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.19+402G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875099 | ||||||
chr3:44875189
|
T | G | 1 | a0005c0005t0009g0032 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.19+492T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875189 | ||||||
chr3:44875198
|
C | A | 2 | a0008c0007t0001g0033a0008c0007t0001g0034 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.19+501C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875198 | ||||||
chr3:44875302
|
T | C | 1 | a0003c0003t0001g0035 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.19+605T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875302 | ||||||
chr3:44875619
|
C | T | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+922C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875619 | ||||||
chr3:44875639
|
A | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+942A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875639 | ||||||
chr3:44875722
|
G | A | 1 | a0002c0002t0002g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.19+1025G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875722 | ||||||
chr3:44875802
|
T | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1105T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875802 | ||||||
chr3:44875966
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1269A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44875966 | ||||||
chr3:44876009
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1312C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876009 | ||||||
chr3:44876036
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1339G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876036 | ||||||
chr3:44876184
|
A | G | 16 | a0004c0004t0001g0264a0010c0009t0005g0263a0010c0009t0005g0265others(13): Show | 16 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+1487A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876184 | ||||||
chr3:44876196
|
C | G | 2 | a0004c0004t0001g0001a0004c0004t0001g0261 | 4 | NA18942.hp2 NA19056.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1499C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876196 | ||||||
chr3:44876243
|
A | G | 129 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(126): Show | 136 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.19+1546A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876243 | ||||||
chr3:44876358
|
C | A | 39 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0045others(36): Show | 43 | HG00099.hp1 HG00609.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.19+1661C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876358 | ||||||
chr3:44876365
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1668A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876365 | ||||||
chr3:44876383
|
G | A | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+1686G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876383 | ||||||
chr3:44876421
|
C | A | 4 | a0004c0004t0001g0145a0004c0004t0001g0146a0004c0004t0001g0147others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1724C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876421 | ||||||
chr3:44876465
|
TGATATGT others(9): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.19+1769_19+1784del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876465 | ||||||
chr3:44876720
|
TAAAGGA | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2028_19+2033del others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44876720 | |||||
chr3:44876989
|
A | G | 1 | a0002c0002t0002g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19+2292A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44876989 | ||||||
chr3:44877275
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2578C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877275 | ||||||
chr3:44877429
|
G | T | 34 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0045others(31): Show | 38 | HG00099.hp1 HG00609.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.19+2732G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877429 | ||||||
chr3:44877457
|
T | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2760T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877457 | ||||||
chr3:44877477
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2780A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877477 | ||||||
chr3:44877569
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.19+2872G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877569 | ||||||
chr3:44877593
|
T | TA | 6 | a0002c0002t0002g0075a0004c0004t0001g0145a0004c0004t0001g0146others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+2908dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877593 | |||||
chr3:44877593
|
TA | T | 11 | a0002c0002t0002g0143a0003c0003t0001g0142a0004c0004t0001g0260others(8): Show | 11 | HG02148.hp1 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+2908delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877593 | |||||
chr3:44877761
|
A | AT | 5 | a0001c0001t0001g0256a0004c0004t0001g0255a0004c0004t0001g0258others(2): Show | 5 | HG01255.hp1 HG01943.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+3067dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44877761 | |||||
chr3:44877917
|
G | A | 45 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0045others(42): Show | 49 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.19+3220G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44877917 | ||||||
chr3:44878345
|
A | G | 1 | a0002c0002t0002g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19+3648A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878345 | ||||||
chr3:44878378
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.19+3681T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878378 | ||||||
chr3:44878444
|
T | TTTA | 3 | a0011c0011t0001g0023a0011c0011t0001g0026a0011c0011t0001g0027 | 3 | HG02895.hp2 HG02896.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.19+3749_19+3750ins others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878444 | |||||
chr3:44878447
|
G | A | 260 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(257): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.19+3750G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878447 | ||||||
chr3:44878447
|
G | T | 3 | a0011c0011t0001g0023a0011c0011t0001g0026a0011c0011t0001g0027 | 3 | HG02895.hp2 HG02896.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.19+3750G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878447 | ||||||
chr3:44878449
|
T | TTTA | 21 | a0002c0002t0002g0019a0002c0002t0002g0036a0002c0002t0002g0077others(18): Show | 24 | HG00735.hp2 HG00738.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.19+3800_19+3802dup others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTA | T | 37 | a0002c0002t0002g0045a0002c0002t0002g0075a0002c0002t0002g0104others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+3800_19+3802del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTATTA | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 28 | HG00099.hp1 HG00408.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.19+3797_19+3802del others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTATTAT others(2): Show |
T | 56 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0149others(53): Show | 63 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.19+3794_19+3802del others(9): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTATTAT others(5): Show |
T | 71 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0150others(68): Show | 73 | HG00609.hp2 HG00733.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+3791_19+3802del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTATTAT others(8): Show |
T | 22 | a0001c0001t0001g0240a0001c0001t0001g0247a0003c0003t0001g0072others(19): Show | 25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+3788_19+3802del others(15): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878449
|
TTTATTAT others(11): Show |
T | 9 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3785_19+3802del others(18): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44878449 | |||||
chr3:44878452
|
A | T | 2 | a0011c0011t0001g0028a0016c0020t0001g0029 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19+3755A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878452 | ||||||
chr3:44878455
|
A | T | 1 | a0016c0020t0001g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19+3758A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878455 | ||||||
chr3:44878461
|
A | T | 1 | a0026c0031t0001g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+3764A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878461 | ||||||
chr3:44878508
|
G | T | 3 | a0011c0011t0001g0025a0011c0011t0001g0026a0011c0011t0001g0027 | 3 | HG02809.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.19+3811G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878508 | ||||||
chr3:44878543
|
C | T | 53 | a0002c0002t0002g0008a0002c0002t0002g0036a0002c0002t0002g0073others(50): Show | 54 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.19+3846C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878543 | ||||||
chr3:44878631
|
C | G | 1 | a0003c0003t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19+3934C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878631 | ||||||
chr3:44878632
|
G | A | 53 | a0002c0002t0002g0008a0002c0002t0002g0036a0002c0002t0002g0073others(50): Show | 54 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.19+3935G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878632 | ||||||
chr3:44878768
|
C | T | 1 | a0006c0015t0003g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19+4071C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878768 | ||||||
chr3:44878943
|
T | C | 5 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(2): Show | 6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+4246T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44878943 | ||||||
chr3:44879025
|
C | T | 1 | a0002c0013t0006g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+4328C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879025 | ||||||
chr3:44879058
|
G | C | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+4361G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879058 | ||||||
chr3:44879066
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.19+4369T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879066 | ||||||
chr3:44879237
|
G | GTC | 6 | a0005c0005t0001g0007a0005c0005t0001g0102a0005c0005t0001g0103others(3): Show | 7 | HG02145.hp2 HG02723.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+4568_19+4569dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | |||||
chr3:44879237
|
GTC | G | 14 | a0001c0001t0001g0248a0002c0018t0002g0002a0003c0003t0001g0011others(11): Show | 16 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.19+4568_19+4569del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | |||||
chr3:44879237
|
GTCTC | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0159others(39): Show | 44 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.19+4566_19+4569del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879237 | |||||
chr3:44879253
|
CTCTCTCT others(9): Show |
C | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19+4558_19+4573del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879253 | |||||
chr3:44879255
|
CTCTCTCT others(5): Show |
C | 1 | a0007c0006t0003g0009 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19+4560_19+4571del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879255 | |||||
chr3:44879255
|
CTCTCTCT others(9): Show |
C | 3 | a0011c0011t0001g0026a0011c0011t0001g0027a0011c0011t0001g0028 | 3 | HG02895.hp2 HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.19+4560_19+4575del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879255 | |||||
chr3:44879257
|
C | A | 1 | a0002c0002t0002g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19+4560C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879257 | ||||||
chr3:44879257
|
CTCTCTCT others(5): Show |
C | 1 | a0006c0010t0003g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+4562_19+4573del others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879257 | |||||
chr3:44879257
|
CTCTCTCT others(9): Show |
C | 4 | a0011c0011t0001g0025a0016c0020t0001g0029a0016c0020t0001g0030others(1): Show | 4 | HG02809.hp1 HG02922.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+4562_19+4577del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879257 | |||||
chr3:44879259
|
C | A | 4 | a0002c0002t0002g0089a0002c0002t0002g0104a0002c0002t0002g0143others(1): Show | 4 | HG02129.hp2 HG02965.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4562C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879259 | ||||||
chr3:44879259
|
CTCTCTCT others(1): Show |
C | 18 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0045others(15): Show | 21 | HG01358.hp2 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.19+4564_19+4571del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879259 | |||||
chr3:44879259
|
CTCTCTCT others(9): Show |
C | 1 | a0011c0011t0001g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19+4564_19+4579del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879259 | |||||
chr3:44879261
|
C | A | 10 | a0002c0002t0002g0089a0002c0002t0002g0104a0002c0002t0002g0120others(7): Show | 10 | HG00140.hp1 HG01071.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+4564C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879261 | ||||||
chr3:44879261
|
C | CTATA | 3 | a0002c0002t0002g0021a0002c0002t0002g0270a0002c0002t0002g0274 | 3 | HG00735.hp1 HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.19+4565_19+4566ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879261 | |||||
chr3:44879261
|
CTCTCTAT others(1): Show |
C | 10 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0002g0076others(7): Show | 10 | HG00408.hp1 HG01975.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+4566_19+4573del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879261 | |||||
chr3:44879263
|
C | A | 36 | a0002c0002t0002g0008a0002c0002t0002g0021a0002c0002t0002g0077others(33): Show | 39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.19+4566C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879263 | ||||||
chr3:44879263
|
C | CTA | 3 | a0002c0013t0006g0168a0005c0005t0001g0101a0008c0007t0001g0034 | 3 | HG01109.hp2 HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | |||||
chr3:44879263
|
C | CTATA | 4 | a0002c0002t0002g0019a0002c0002t0002g0022a0002c0002t0002g0111others(1): Show | 5 | HG00280.hp1 HG01106.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | |||||
chr3:44879263
|
C | CTATATA | 3 | a0002c0002t0002g0112a0002c0002t0002g0113a0003c0003t0001g0286 | 3 | HG01168.hp2 HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.19+4567_19+4568ins others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | |||||
chr3:44879263
|
CTCTA | C | 39 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0160others(36): Show | 41 | HG00558.hp2 HG00673.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.19+4568_19+4571del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | |||||
chr3:44879263
|
CTCTATAT others(1): Show |
C | 4 | a0003c0003t0001g0048a0003c0003t0001g0070a0006c0010t0003g0006others(1): Show | 5 | HG00609.hp1 HG02132.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4568_19+4575del others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879263 | |||||
chr3:44879265
|
C | A | 79 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(76): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.19+4568C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879265 | ||||||
chr3:44879265
|
C | CTA | 8 | a0001c0001t0001g0130a0002c0002t0002g0137a0002c0013t0006g0156others(5): Show | 9 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4589_19+4590dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879265
|
C | CTATA | 4 | a0002c0002t0002g0075a0002c0002t0002g0281a0005c0005t0001g0119others(1): Show | 4 | HG01496.hp1 HG02258.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4587_19+4590dup others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879265
|
C | CTATATA | 3 | a0002c0002t0002g0282a0002c0002t0002g0290a0002c0002t0010g0283 | 3 | HG02300.hp1 HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.19+4585_19+4590dup others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879265
|
C | CTCTCTAT others(3): Show |
1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+4569_19+4570ins others(10): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879265
|
CTA | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG02056.hp1 HG02145.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+4589_19+4590del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879265
|
CTATA | C | 40 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0149others(37): Show | 43 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.19+4587_19+4590del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879265 | |||||
chr3:44879267
|
A | C | 7 | a0002c0002t0002g0073a0002c0002t0002g0122a0005c0005t0001g0103others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+4570A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879267 | ||||||
chr3:44879269
|
A | C | 5 | a0001c0001t0001g0233a0001c0001t0001g0234a0009c0008t0004g0157others(2): Show | 5 | HG02056.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4572A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879269 | ||||||
chr3:44879271
|
A | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0167a0001c0001t0001g0230others(6): Show | 10 | HG01952.hp2 HG02055.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+4574A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879271 | ||||||
chr3:44879273
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19+4576A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879273 | ||||||
chr3:44879286
|
T | G | 1 | a0002c0002t0002g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19+4589T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879286 | ||||||
chr3:44879309
|
T | A | 173 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(170): Show | 184 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.19+4612T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879309 | ||||||
chr3:44879313
|
T | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0232 | 2 | HG03710.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.19+4616T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879313 | ||||||
chr3:44879388
|
C | CCTCTGCC others(159): Show |
2 | a0002c0002t0002g0106a0002c0002t0002g0107 | 2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.19+4757_19+4758ins others(166): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879388 | |||||
chr3:44879455
|
T | C | 265 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(262): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.19+4758T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879455 | ||||||
chr3:44879470
|
C | CTTTT | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4774_19+4775ins others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879470 | |||||
chr3:44879472
|
A | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4775A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879472 | ||||||
chr3:44879473
|
A | AT | 7 | a0001c0001t0001g0187a0001c0001t0001g0199a0003c0003t0001g0072others(4): Show | 7 | HG01361.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+4793dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879473 | |||||
chr3:44879473
|
A | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4776A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879473 | ||||||
chr3:44879473
|
AT | A | 7 | a0001c0001t0001g0149a0004c0004t0001g0264a0010c0009t0005g0153others(4): Show | 7 | HG02258.hp2 HG02615.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+4793delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44879473 | |||||
chr3:44879511
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0252 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.19+4814C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879511 | ||||||
chr3:44879666
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+4969C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879666 | ||||||
chr3:44879819
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+5122A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44879819 | ||||||
chr3:44880028
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-5297G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880028 | ||||||
chr3:44880058
|
C | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-5267C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880058 | ||||||
chr3:44880074
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.20-5251T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880074 | ||||||
chr3:44880433
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4892C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880433 | ||||||
chr3:44880470
|
C | T | 1 | a0002c0002t0002g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.20-4855C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880470 | ||||||
chr3:44880542
|
G | T | 5 | a0010c0009t0005g0263a0010c0009t0005g0265a0010c0009t0005g0266others(2): Show | 5 | HG02258.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4783G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880542 | ||||||
chr3:44880649
|
A | C | 128 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.20-4676A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880649 | ||||||
chr3:44880654
|
T | C | 3 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168 | 3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.20-4671T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880654 | ||||||
chr3:44880669
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.20-4656A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880669 | ||||||
chr3:44880698
|
T | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4627T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880698 | ||||||
chr3:44880987
|
G | A | 2 | a0004c0004t0001g0260a0007c0006t0003g0040 | 2 | HG02148.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.20-4338G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880987 | ||||||
chr3:44880997
|
C | T | 1 | a0003c0003t0001g0142 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20-4328C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880997 | ||||||
chr3:44880998
|
G | A | 5 | a0010c0009t0005g0263a0010c0009t0005g0265a0010c0009t0005g0266others(2): Show | 5 | HG02258.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-4327G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44880998 | ||||||
chr3:44881055
|
T | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4270T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881055 | ||||||
chr3:44881057
|
T | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4268T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881057 | ||||||
chr3:44881058
|
G | A | 10 | a0003c0003t0001g0049a0011c0011t0001g0023a0011c0011t0001g0025others(7): Show | 10 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-4267G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881058 | ||||||
chr3:44881060
|
A | ATAAAAAA others(5): Show |
9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4265_20-4264ins others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881060 | ||||||
chr3:44881063
|
GCA | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4260_20-4259del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44881063 | |||||
chr3:44881066
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4259C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881066 | ||||||
chr3:44881067
|
T | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4258T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881067 | ||||||
chr3:44881068
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-4257A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881068 | ||||||
chr3:44881100
|
A | T | 1 | a0017c0024t0001g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20-4225A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881100 | ||||||
chr3:44881146
|
G | A | 1 | a0004c0004t0001g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.20-4179G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881146 | ||||||
chr3:44881243
|
C | G | 4 | a0006c0015t0003g0133a0006c0015t0008g0123a0006c0015t0008g0124others(1): Show | 5 | HG01884.hp2 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-4082C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881243 | ||||||
chr3:44881357
|
T | C | 3 | a0004c0004t0001g0264a0004c0004t0001g0291a0004c0004t0001g0292 | 3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.20-3968T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881357 | ||||||
chr3:44881366
|
T | C | 2 | a0002c0002t0002g0021a0002c0002t0002g0022 | 2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.20-3959T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881366 | ||||||
chr3:44881533
|
G | A | 1 | a0003c0003t0001g0057 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.20-3792G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881533 | ||||||
chr3:44881576
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-3749C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881576 | ||||||
chr3:44881597
|
G | A | 1 | a0003c0003t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.20-3728G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881597 | ||||||
chr3:44881696
|
C | T | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.20-3629C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881696 | ||||||
chr3:44881852
|
G | C | 1 | a0017c0024t0001g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20-3473G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881852 | ||||||
chr3:44881856
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.20-3469C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881856 | ||||||
chr3:44881911
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-3414G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44881911 | ||||||
chr3:44882049
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.20-3276T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882049 | ||||||
chr3:44882057
|
C | CT | 97 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0008others(94): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.20-3247dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | |||||
chr3:44882057
|
C | CTT | 19 | a0002c0002t0002g0036a0002c0002t0002g0065a0002c0002t0002g0087others(16): Show | 19 | HG02055.hp2 HG02074.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.20-3248_20-3247dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | |||||
chr3:44882057
|
C | CTTT | 18 | a0001c0001t0001g0150a0001c0001t0001g0151a0003c0003t0001g0052others(15): Show | 20 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.20-3249_20-3247dup others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | |||||
chr3:44882057
|
C | CTTTT | 91 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(88): Show | 97 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.20-3250_20-3247dup others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | |||||
chr3:44882057
|
C | CTTTTT | 38 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0001g0171others(35): Show | 39 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.20-3251_20-3247dup others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 44882057 | |||||
chr3:44882136
|
A | G | 2 | a0002c0002t0002g0290a0003c0003t0001g0286 | 2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.20-3189A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882136 | ||||||
chr3:44882295
|
G | T | 1 | a0003c0003t0001g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.20-3030G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882295 | ||||||
chr3:44882367
|
G | C | 15 | a0010c0009t0005g0263a0010c0009t0005g0265a0010c0009t0005g0266others(12): Show | 15 | HG02258.hp2 HG02809.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-2958G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882367 | ||||||
chr3:44882414
|
C | T | 4 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-2911C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882414 | ||||||
chr3:44882488
|
A | C | 4 | a0004c0004t0001g0145a0004c0004t0001g0146a0004c0004t0001g0147others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2837A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882488 | ||||||
chr3:44882526
|
G | A | 2 | a0002c0002t0002g0281a0002c0002t0002g0284 | 2 | HG00140.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.20-2799G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882526 | ||||||
chr3:44882764
|
C | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2561C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882764 | ||||||
chr3:44882936
|
G | A | 1 | a0003c0003t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.20-2389G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44882936 | ||||||
chr3:44883374
|
G | T | 1 | a0010c0009t0005g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-1951G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883374 | ||||||
chr3:44883409
|
G | A | 22 | a0001c0001t0001g0130a0004c0004t0001g0126a0005c0005t0001g0007others(19): Show | 24 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-1916G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883409 | ||||||
chr3:44883571
|
C | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1754C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883571 | ||||||
chr3:44883624
|
C | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1701C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883624 | ||||||
chr3:44883704
|
G | A | 1 | a0002c0002t0002g0077 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.20-1621G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883704 | ||||||
chr3:44883745
|
C | T | 1 | a0002c0002t0002g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.20-1580C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883745 | ||||||
chr3:44883856
|
T | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1469T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883856 | ||||||
chr3:44883913
|
T | G | 1 | a0004c0004t0001g0259 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.20-1412T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883913 | ||||||
chr3:44883942
|
G | T | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.20-1383G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883942 | ||||||
chr3:44883943
|
T | A | 1 | a0002c0002t0002g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.20-1382T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883943 | ||||||
chr3:44883982
|
G | A | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.20-1343G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44883982 | ||||||
chr3:44884071
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1254C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884071 | ||||||
chr3:44884113
|
T | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1212T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884113 | ||||||
chr3:44884139
|
C | A | 9 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(6): Show | 11 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1186C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884139 | ||||||
chr3:44884498
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.20-827T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884498 | ||||||
chr3:44884643
|
C | A | 1 | a0005c0005t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-682C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884643 | ||||||
chr3:44884676
|
T | C | 1 | a0022c0026t0006g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-649T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884676 | ||||||
chr3:44884692
|
G | A | 7 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(4): Show | 7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-633G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884692 | ||||||
chr3:44884728
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-597C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884728 | ||||||
chr3:44884918
|
T | C | 4 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-407T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884918 | ||||||
chr3:44884975
|
A | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-350A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44884975 | ||||||
chr3:44885196
|
G | A | 4 | a0004c0004t0001g0017a0004c0004t0001g0235a0004c0004t0001g0236others(1): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-129G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44885196 | ||||||
chr3:44885230
|
C | G | 1 | a0004c0004t0001g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.20-95C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 1/13 | chr3 | 44885230 | ||||||
chr3:44885565
|
T | C | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.193+67T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44885565 | ||||||
chr3:44885675
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193+177C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44885675 | ||||||
chr3:44886112
|
G | A | 16 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(13): Show | 18 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.193+614G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886112 | ||||||
chr3:44886198
|
G | C | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.193+700G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886198 | ||||||
chr3:44886242
|
G | A | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.193+744G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886242 | ||||||
chr3:44886249
|
T | TAGG | 207 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(204): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.193+753_193+754ins others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 44886249 | |||||
chr3:44886287
|
G | T | 1 | a0003c0003t0001g0057 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.193+789G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886287 | ||||||
chr3:44886340
|
CA | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.193+851delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 44886340 | |||||
chr3:44886397
|
C | T | 26 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(23): Show | 28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.193+899C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886397 | ||||||
chr3:44886782
|
G | T | 2 | a0026c0031t0001g0031a0027c0032t0001g0024 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.194-907G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886782 | ||||||
chr3:44886875
|
C | T | 1 | a0007c0006t0003g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194-814C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886875 | ||||||
chr3:44886992
|
T | C | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 32 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.194-697T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44886992 | ||||||
chr3:44887331
|
G | A | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.194-358G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887331 | ||||||
chr3:44887394
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-295C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887394 | ||||||
chr3:44887426
|
G | A | 26 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(23): Show | 28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-263G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887426 | ||||||
chr3:44887622
|
G | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0161others(6): Show | 9 | HG00558.hp2 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-67G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 2/13 | chr3 | 44887622 | ||||||
chr3:44888104
|
C | A | 5 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(2): Show | 6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+309C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888104 | ||||||
chr3:44888130
|
C | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+335C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888130 | ||||||
chr3:44888228
|
G | A | 26 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(23): Show | 28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.300+433G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888228 | ||||||
chr3:44888239
|
T | C | 5 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(2): Show | 6 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+444T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888239 | ||||||
chr3:44888251
|
G | A | 3 | a0004c0004t0001g0264a0004c0004t0001g0291a0004c0004t0001g0292 | 3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.300+456G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888251 | ||||||
chr3:44888318
|
C | A | 2 | a0003c0003t0001g0042a0008c0007t0001g0210 | 2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.300+523C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888318 | ||||||
chr3:44888419
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+624C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888419 | ||||||
chr3:44888522
|
C | T | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.300+727C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888522 | ||||||
chr3:44888544
|
T | C | 1 | a0003c0003t0001g0082 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.300+749T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888544 | ||||||
chr3:44888623
|
G | A | 1 | a0002c0002t0002g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.300+828G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888623 | ||||||
chr3:44888714
|
C | T | 1 | a0002c0002t0002g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.300+919C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888714 | ||||||
chr3:44888825
|
C | G | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.300+1030C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44888825 | ||||||
chr3:44889170
|
T | TA | 77 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0149others(74): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.301-1399dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAA | 34 | a0001c0001t0001g0013a0001c0001t0001g0159a0001c0001t0001g0160others(31): Show | 35 | HG00408.hp2 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.301-1400_301-1399d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAAA | 18 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0171others(15): Show | 18 | HG01261.hp2 HG01978.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-1401_301-1399d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAAAA | 11 | a0001c0001t0001g0151a0001c0001t0001g0176a0001c0001t0001g0190others(8): Show | 12 | HG00558.hp2 HG01433.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1402_301-1399d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAAAAAAA others(5): Show |
2 | a0003c0003t0001g0011a0003c0003t0001g0140 | 3 | HG02559.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.300+1398_301-1399d others(14): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAAAAAAA others(6): Show |
2 | a0003c0003t0001g0139a0008c0007t0001g0100 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.300+1397_301-1399d others(15): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
T | TAAAAAAA others(7): Show |
1 | a0003c0003t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.300+1396_301-1399d others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TA | T | 13 | a0001c0001t0001g0130a0001c0001t0001g0209a0001c0001t0001g0227others(10): Show | 14 | HG01943.hp1 HG02004.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-1399delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAA | T | 9 | a0004c0004t0001g0238a0006c0015t0003g0133a0006c0015t0008g0123others(6): Show | 10 | HG01515.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-1400_301-1399d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAAAA | T | 5 | a0002c0002t0010g0018a0004c0004t0001g0243a0004c0004t0001g0246others(2): Show | 6 | HG01167.hp1 HG02148.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-1402_301-1399d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAAAAA | T | 21 | a0004c0004t0001g0001a0004c0004t0001g0017a0004c0004t0001g0126others(18): Show | 24 | HG00639.hp1 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-1403_301-1399d others(7): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAAAAAA | T | 28 | a0001c0001t0001g0247a0004c0004t0001g0146a0004c0004t0001g0222others(25): Show | 31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.300+1404_301-1399d others(8): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAAAAAAA others(3): Show |
T | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.300+1400_301-1399d others(12): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889170
|
TAAAAAAA others(11): Show |
T | 11 | a0001c0014t0001g0015a0001c0014t0001g0226a0011c0011t0001g0023others(8): Show | 12 | HG02071.hp1 HG02129.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+1392_301-1399d others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889170 | |||||
chr3:44889215
|
G | A | 2 | a0006c0010t0003g0006a0006c0010t0003g0053 | 3 | HG03516.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.301-1388G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889215 | ||||||
chr3:44889228
|
C | T | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.301-1375C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889228 | ||||||
chr3:44889319
|
C | T | 9 | a0003c0003t0001g0072a0006c0010t0003g0037a0006c0010t0003g0058others(6): Show | 10 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-1284C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889319 | ||||||
chr3:44889332
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-1271A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889332 | ||||||
chr3:44889357
|
A | ATCT | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-1244_301-1242d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889357 | |||||
chr3:44889607
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-996A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889607 | ||||||
chr3:44889722
|
A | T | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.301-881A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889722 | ||||||
chr3:44889737
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0233 | 2 | HG02080.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.301-866C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889737 | ||||||
chr3:44889792
|
GT | G | 13 | a0003c0003t0001g0011a0003c0003t0001g0138a0003c0003t0001g0139others(10): Show | 14 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-802delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 44889792 | |||||
chr3:44889992
|
C | G | 1 | a0003c0003t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.301-611C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44889992 | ||||||
chr3:44890042
|
A | C | 1 | a0001c0014t0001g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301-561A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890042 | ||||||
chr3:44890200
|
C | T | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.301-403C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890200 | ||||||
chr3:44890447
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-156G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890447 | ||||||
chr3:44890522
|
C | T | 2 | a0001c0001t0001g0150a0003c0003t0001g0003 | 3 | HG03491.hp2 HG03492.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.301-81C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890522 | ||||||
chr3:44890532
|
T | C | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301-71T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890532 | ||||||
chr3:44890569
|
G | C | 2 | a0003c0003t0001g0047a0003c0003t0001g0066 | 2 | HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.301-34G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 3/13 | chr3 | 44890569 | ||||||
chr3:44890778
|
C | T | 89 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(86): Show | 93 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.430+46C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890778 | ||||||
chr3:44890797
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0204 | 2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.430+65T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890797 | ||||||
chr3:44890816
|
T | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+84T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890816 | ||||||
chr3:44890883
|
A | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+151A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890883 | ||||||
chr3:44890908
|
C | T | 3 | a0006c0015t0003g0133a0006c0015t0008g0123a0006c0015t0008g0124 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.430+176C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890908 | ||||||
chr3:44890959
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+227C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44890959 | ||||||
chr3:44891009
|
C | T | 1 | a0003c0003t0001g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.430+277C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891009 | ||||||
chr3:44891368
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430+636T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891368 | ||||||
chr3:44891370
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430+638A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891370 | ||||||
chr3:44891371
|
C | CCT | 208 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(205): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.430+639_430+640ins others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891371 | ||||||
chr3:44891442
|
TATC | T | 134 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(131): Show | 141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.430+714_430+716del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891442 | |||||
chr3:44891512
|
T | TAC | 9 | a0001c0001t0001g0216a0008c0007t0001g0055a0011c0011t0001g0023others(6): Show | 9 | HG00099.hp1 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+808_430+809dup others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | |||||
chr3:44891512
|
TAC | T | 121 | a0001c0001t0001g0209a0001c0001t0001g0227a0001c0001t0001g0252others(118): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.430+808_430+809del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | |||||
chr3:44891512
|
TACAC | T | 72 | a0001c0001t0001g0130a0001c0001t0001g0195a0001c0001t0001g0247others(69): Show | 79 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.430+806_430+809del others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891512 | |||||
chr3:44891542
|
A | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+810A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891542 | ||||||
chr3:44891560
|
C | G | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.430+828C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891560 | ||||||
chr3:44891697
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+965A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891697 | ||||||
chr3:44891701
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+969G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891701 | ||||||
chr3:44891757
|
G | A | 1 | a0003c0003t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430+1025G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891757 | ||||||
chr3:44891762
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.430+1030T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891762 | ||||||
chr3:44891763
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.430+1031G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891763 | ||||||
chr3:44891832
|
G | A | 1 | a0004c0004t0001g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.430+1100G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891832 | ||||||
chr3:44891843
|
C | T | 1 | a0002c0018t0002g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.430+1111C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891843 | ||||||
chr3:44891847
|
C | T | 2 | a0015c0019t0002g0127a0015c0019t0002g0131 | 2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.430+1115C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891847 | ||||||
chr3:44891963
|
GA | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1242delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44891963 | |||||
chr3:44891971
|
A | G | 1 | a0002c0002t0002g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.430+1239A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891971 | ||||||
chr3:44891986
|
C | T | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.430+1254C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44891986 | ||||||
chr3:44892119
|
C | G | 210 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(207): Show | 224 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.430+1387C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892119 | ||||||
chr3:44892172
|
C | T | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1405C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892172 | ||||||
chr3:44892206
|
T | C | 209 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(206): Show | 222 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.431-1371T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892206 | ||||||
chr3:44892207
|
G | A | 1 | a0002c0002t0002g0062 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.431-1370G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892207 | ||||||
chr3:44892234
|
G | A | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-1343G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892234 | ||||||
chr3:44892259
|
A | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1318A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892259 | ||||||
chr3:44892283
|
A | T | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1294A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892283 | ||||||
chr3:44892285
|
T | A | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-1292T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892285 | ||||||
chr3:44892362
|
AT | A | 141 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 148 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.431-1198delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 44892362 | |||||
chr3:44892385
|
G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.431-1192G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892385 | ||||||
chr3:44892424
|
G | A | 1 | a0004c0004t0001g0242 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.431-1153G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892424 | ||||||
chr3:44892434
|
G | A | 2 | a0005c0005t0001g0128a0005c0005t0001g0129 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-1143G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892434 | ||||||
chr3:44892576
|
G | T | 20 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(17): Show | 22 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-1001G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892576 | ||||||
chr3:44892674
|
C | T | 5 | a0004c0004t0001g0145a0004c0004t0001g0146a0004c0004t0001g0147others(2): Show | 5 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-903C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892674 | ||||||
chr3:44892789
|
T | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-788T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892789 | ||||||
chr3:44892790
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-787A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892790 | ||||||
chr3:44892831
|
G | T | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.431-746G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892831 | ||||||
chr3:44892889
|
A | G | 26 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(23): Show | 28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.431-688A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892889 | ||||||
chr3:44892929
|
G | A | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.431-648G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44892929 | ||||||
chr3:44893267
|
C | G | 1 | a0004c0004t0001g0259 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.431-310C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893267 | ||||||
chr3:44893396
|
G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.431-181G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893396 | ||||||
chr3:44893404
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-173G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893404 | ||||||
chr3:44893488
|
T | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-89T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893488 | ||||||
chr3:44893527
|
C | T | 87 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 91 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.431-50C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 4/13 | chr3 | 44893527 | ||||||
chr3:44893753
|
G | A | 1 | a0006c0015t0008g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.549+58G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893753 | ||||||
chr3:44893826
|
A | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+131A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893826 | ||||||
chr3:44893933
|
C | CGGCTCTC others(13): Show |
183 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(180): Show | 193 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.549+257_549+258ins others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44893933 | |||||
chr3:44893945
|
A | ACCCCCCA others(14): Show |
1 | a0001c0001t0001g0184 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.549+257_549+258ins others(21): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44893945 | |||||
chr3:44893954
|
A | G | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+259A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893954 | ||||||
chr3:44893973
|
T | C | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+278T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44893973 | ||||||
chr3:44894063
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.549+368C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894063 | ||||||
chr3:44894108
|
C | T | 3 | a0004c0004t0001g0264a0004c0004t0001g0291a0004c0004t0001g0292 | 3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.549+413C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894108 | ||||||
chr3:44894111
|
G | A | 1 | a0018c0025t0011g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.549+416G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894111 | ||||||
chr3:44894114
|
T | C | 1 | a0002c0002t0002g0293 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.549+419T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894114 | ||||||
chr3:44894171
|
TCCCCCAT others(13): Show |
T | 8 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(5): Show | 8 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.549+532_549+551del others(20): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894171 | |||||
chr3:44894235
|
C | G | 1 | a0001c0001t0001g0250 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.549+540C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894235 | ||||||
chr3:44894258
|
T | C | 284 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(281): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.549+563T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894258 | ||||||
chr3:44894322
|
C | G | 1 | a0007c0006t0003g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.549+627C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894322 | ||||||
chr3:44894329
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.549+634C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894329 | ||||||
chr3:44894440
|
CAAGCACT others(9): Show |
C | 1 | a0008c0007t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.549+776_549+791del others(16): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894440 | |||||
chr3:44894465
|
T | C | 5 | a0005c0005t0001g0010a0005c0005t0001g0119a0005c0005t0001g0128others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+770T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894465 | ||||||
chr3:44894512
|
C | CT | 208 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(205): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.549+818dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 44894512 | |||||
chr3:44894578
|
C | G | 20 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(17): Show | 22 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.549+883C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894578 | ||||||
chr3:44894593
|
G | A | 30 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(27): Show | 31 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.549+898G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894593 | ||||||
chr3:44894643
|
C | G | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+948C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894643 | ||||||
chr3:44894660
|
T | A | 1 | a0022c0026t0006g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+965T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894660 | ||||||
chr3:44894890
|
C | G | 86 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 90 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.549+1195C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894890 | ||||||
chr3:44894938
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+1243C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894938 | ||||||
chr3:44894995
|
C | T | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 130 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.549+1300C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44894995 | ||||||
chr3:44895166
|
G | A | 6 | a0007c0006t0003g0009a0007c0006t0003g0038a0007c0006t0003g0039others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+1471G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895166 | ||||||
chr3:44895244
|
G | T | 2 | a0001c0001t0001g0195a0017c0024t0001g0186 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.550-1465G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895244 | ||||||
chr3:44895310
|
A | G | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-1399A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895310 | ||||||
chr3:44895776
|
G | A | 1 | a0002c0002t0002g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.550-933G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895776 | ||||||
chr3:44895879
|
G | A | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-830G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895879 | ||||||
chr3:44895901
|
T | G | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-808T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44895901 | ||||||
chr3:44896001
|
C | T | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-708C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896001 | ||||||
chr3:44896124
|
T | G | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-585T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896124 | ||||||
chr3:44896137
|
G | A | 4 | a0004c0004t0001g0145a0004c0004t0001g0146a0004c0004t0001g0147others(1): Show | 4 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-572G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896137 | ||||||
chr3:44896179
|
T | C | 1 | a0009c0008t0004g0253 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.550-530T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896179 | ||||||
chr3:44896198
|
G | A | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-511G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896198 | ||||||
chr3:44896214
|
C | T | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-495C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896214 | ||||||
chr3:44896268
|
C | T | 28 | a0003c0003t0001g0050a0003c0003t0014g0054a0005c0005t0001g0007others(25): Show | 30 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.550-441C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896268 | ||||||
chr3:44896273
|
G | T | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-436G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896273 | ||||||
chr3:44896339
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.550-370G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896339 | ||||||
chr3:44896355
|
C | T | 2 | a0008c0007t0001g0033a0008c0007t0001g0034 | 2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.550-354C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896355 | ||||||
chr3:44896521
|
C | T | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.550-188C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896521 | ||||||
chr3:44896631
|
T | C | 1 | a0005c0005t0009g0125 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.550-78T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 5/13 | chr3 | 44896631 | ||||||
chr3:44896986
|
G | T | 1 | a0001c0001t0001g0164 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.657+170G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44896986 | ||||||
chr3:44897000
|
CT | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0221a0001c0001t0001g0228others(15): Show | 18 | HG01070.hp1 HG01167.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.657+205delT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | |||||
chr3:44897000
|
CTT | C | 180 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.657+204_657+205del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | |||||
chr3:44897000
|
CTTT | C | 13 | a0001c0001t0001g0155a0001c0001t0001g0164a0003c0003t0001g0042others(10): Show | 15 | HG01168.hp1 HG01255.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.657+203_657+205del others(3): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44897000 | |||||
chr3:44897007
|
T | C | 4 | a0010c0009t0005g0153a0010c0009t0005g0265a0010c0009t0005g0266others(1): Show | 4 | HG02976.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+191T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897007 | ||||||
chr3:44897047
|
T | C | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+231T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897047 | ||||||
chr3:44897057
|
G | A | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+241G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897057 | ||||||
chr3:44897058
|
C | T | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+242C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897058 | ||||||
chr3:44897094
|
A | C | 292 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(289): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.657+278A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897094 | ||||||
chr3:44897128
|
C | T | 1 | a0006c0010t0003g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657+312C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897128 | ||||||
chr3:44897152
|
A | G | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657+336A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897152 | ||||||
chr3:44897154
|
G | T | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+338G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897154 | ||||||
chr3:44897293
|
C | T | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+477C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897293 | ||||||
chr3:44897295
|
C | T | 1 | a0012c0012t0001g0118 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.657+479C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897295 | ||||||
chr3:44897628
|
T | C | 65 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0008others(62): Show | 68 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.657+812T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897628 | ||||||
chr3:44897770
|
T | C | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+954T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897770 | ||||||
chr3:44897868
|
G | T | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.657+1052G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897868 | ||||||
chr3:44897945
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.657+1129G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44897945 | ||||||
chr3:44898064
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.657+1248G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898064 | ||||||
chr3:44898067
|
G | A | 9 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(6): Show | 9 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.657+1251G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898067 | ||||||
chr3:44898096
|
A | G | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.657+1280A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898096 | ||||||
chr3:44898239
|
C | T | 2 | a0002c0002t0002g0134a0002c0002t0002g0143 | 2 | HG01074.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.657+1423C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898239 | ||||||
chr3:44898257
|
G | C | 1 | a0002c0002t0002g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.657+1441G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898257 | ||||||
chr3:44898275
|
T | C | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+1459T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898275 | ||||||
chr3:44898280
|
CA | C | 278 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(275): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.657+1482delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 44898280 | |||||
chr3:44898358
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.657+1542C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898358 | ||||||
chr3:44898441
|
T | C | 10 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(7): Show | 10 | HG02809.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+1625T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898441 | ||||||
chr3:44898539
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.657+1723A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898539 | ||||||
chr3:44898615
|
G | A | 10 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(7): Show | 12 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+1799G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898615 | ||||||
chr3:44898654
|
G | C | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+1838G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898654 | ||||||
chr3:44898662
|
C | T | 1 | a0027c0032t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657+1846C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898662 | ||||||
chr3:44898834
|
C | T | 30 | a0001c0001t0001g0195a0001c0001t0001g0247a0004c0004t0001g0001others(27): Show | 33 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.657+2018C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898834 | ||||||
chr3:44898921
|
A | G | 152 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(149): Show | 160 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.657+2105A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44898921 | ||||||
chr3:44899108
|
A | G | 1 | a0022c0026t0006g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657+2292A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899108 | ||||||
chr3:44899110
|
A | G | 31 | a0002c0002t0002g0045a0002c0002t0002g0062a0002c0002t0002g0067others(28): Show | 32 | HG00609.hp1 HG00741.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+2294A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899110 | ||||||
chr3:44899127
|
C | G | 2 | a0011c0011t0001g0026a0011c0011t0001g0027 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.657+2311C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899127 | ||||||
chr3:44899145
|
G | A | 2 | a0004c0004t0001g0246a0004c0023t0001g0245 | 2 | HG02523.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.657+2329G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899145 | ||||||
chr3:44899434
|
C | T | 1 | a0020c0021t0001g0254 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.658-2090C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899434 | ||||||
chr3:44899489
|
C | A | 1 | a0006c0015t0003g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.658-2035C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899489 | ||||||
chr3:44899566
|
G | T | 3 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0120 | 3 | HG01071.hp2 HG01168.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.658-1958G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899566 | ||||||
chr3:44899643
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.658-1881C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899643 | ||||||
chr3:44899658
|
G | A | 35 | a0001c0001t0001g0130a0001c0001t0001g0195a0001c0001t0001g0209others(32): Show | 38 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.658-1866G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899658 | ||||||
chr3:44899666
|
T | A | 8 | a0002c0002t0002g0067a0002c0002t0002g0068a0003c0003t0001g0050others(5): Show | 8 | HG01496.hp2 HG02074.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-1858T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899666 | ||||||
chr3:44899958
|
C | T | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.658-1566C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899958 | ||||||
chr3:44899973
|
G | A | 1 | a0021c0030t0003g0268 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.658-1551G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44899973 | ||||||
chr3:44900040
|
C | A | 157 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(154): Show | 168 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.658-1484C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900040 | ||||||
chr3:44900090
|
G | A | 6 | a0010c0009t0005g0153a0010c0009t0005g0263a0010c0009t0005g0265others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-1434G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900090 | ||||||
chr3:44900368
|
C | G | 166 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(163): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-1156C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900368 | ||||||
chr3:44900485
|
A | G | 137 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(134): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.658-1039A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900485 | ||||||
chr3:44900629
|
C | T | 171 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 183 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.658-895C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900629 | ||||||
chr3:44900845
|
G | A | 166 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(163): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-679G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900845 | ||||||
chr3:44900991
|
C | A | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-533C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44900991 | ||||||
chr3:44901004
|
T | C | 167 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.658-520T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901004 | ||||||
chr3:44901096
|
C | T | 1 | a0008c0007t0001g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.658-428C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901096 | ||||||
chr3:44901182
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-342G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901182 | ||||||
chr3:44901279
|
T | C | 166 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(163): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.658-245T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901279 | ||||||
chr3:44901296
|
G | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0204 | 2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.658-228G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901296 | ||||||
chr3:44901315
|
C | A | 7 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(4): Show | 7 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.658-209C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901315 | ||||||
chr3:44901315
|
C | G | 171 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 183 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.658-209C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 6/13 | chr3 | 44901315 | ||||||
chr3:44902083
|
T | A | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.971+152T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902083 | ||||||
chr3:44902121
|
T | C | 5 | a0012c0012t0001g0083a0012c0012t0001g0115a0012c0012t0001g0117others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+190T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902121 | ||||||
chr3:44902234
|
T | C | 157 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(154): Show | 168 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.971+303T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902234 | ||||||
chr3:44902389
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.971+458G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902389 | ||||||
chr3:44902470
|
C | T | 156 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.971+539C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902470 | ||||||
chr3:44902494
|
G | A | 15 | a0005c0005t0001g0007a0005c0005t0001g0010a0005c0005t0001g0088others(12): Show | 17 | HG00642.hp2 HG00741.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+563G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902494 | ||||||
chr3:44902663
|
CCT | C | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.971+735_971+736del others(2): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 44902663 | |||||
chr3:44902908
|
T | A | 3 | a0004c0004t0001g0264a0004c0004t0001g0291a0004c0004t0001g0292 | 3 | HG02572.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.972-976T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44902908 | ||||||
chr3:44903064
|
A | G | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-820A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903064 | ||||||
chr3:44903128
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.972-756C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903128 | ||||||
chr3:44903251
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-633A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903251 | ||||||
chr3:44903289
|
T | C | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-595T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903289 | ||||||
chr3:44903351
|
T | C | 1 | a0008c0007t0012g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.972-533T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903351 | ||||||
chr3:44903571
|
C | T | 81 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 85 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.972-313C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903571 | ||||||
chr3:44903575
|
T | C | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-309T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903575 | ||||||
chr3:44903629
|
G | A | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.972-255G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903629 | ||||||
chr3:44903667
|
C | T | 7 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(4): Show | 7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-217C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903667 | ||||||
chr3:44903853
|
C | T | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.972-31C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 8/13 | chr3 | 44903853 | ||||||
chr3:44904099
|
A | G | 1 | a0002c0018t0002g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1075+112A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904099 | ||||||
chr3:44904202
|
T | C | 1 | a0004c0004t0001g0239 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1075+215T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904202 | ||||||
chr3:44904233
|
GGTT | G | 53 | a0002c0002t0002g0045a0002c0002t0002g0062a0003c0003t0001g0003others(50): Show | 57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+247_1075+249d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904233 | ||||||
chr3:44904237
|
C | T | 53 | a0002c0002t0002g0045a0002c0002t0002g0062a0003c0003t0001g0003others(50): Show | 57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+250C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904237 | ||||||
chr3:44904238
|
C | A | 53 | a0002c0002t0002g0045a0002c0002t0002g0062a0003c0003t0001g0003others(50): Show | 57 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+251C>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904238 | ||||||
chr3:44904248
|
A | G | 187 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(184): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1075+261A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904248 | ||||||
chr3:44904501
|
C | T | 1 | a0019c0022t0001g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1075+514C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904501 | ||||||
chr3:44904608
|
G | C | 12 | a0001c0001t0001g0195a0003c0003t0001g0079a0003c0003t0001g0082others(9): Show | 12 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+621G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904608 | ||||||
chr3:44904676
|
T | A | 1 | a0002c0002t0002g0270 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1075+689T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904676 | ||||||
chr3:44904918
|
G | A | 1 | a0008c0007t0001g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1075+931G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44904918 | ||||||
chr3:44905106
|
T | C | 1 | a0003c0003t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1075+1119T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905106 | ||||||
chr3:44905279
|
C | G | 1 | a0003c0003t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1075+1292C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905279 | ||||||
chr3:44905291
|
C | CT | 196 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(193): Show | 209 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1075+1316dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 44905291 | |||||
chr3:44905753
|
A | G | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1076-1196A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905753 | ||||||
chr3:44905838
|
G | C | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-1111G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905838 | ||||||
chr3:44905839
|
C | CT | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-1110_1076-110 others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905839 | ||||||
chr3:44905840
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1076-1109A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905840 | ||||||
chr3:44905954
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1076-995C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44905954 | ||||||
chr3:44906062
|
G | A | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-887G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906062 | ||||||
chr3:44906129
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1076-820G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906129 | ||||||
chr3:44906142
|
C | T | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-807C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906142 | ||||||
chr3:44906265
|
G | A | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-684G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906265 | ||||||
chr3:44906378
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1076-571A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906378 | ||||||
chr3:44906466
|
AACAGCTT others(15): Show |
A | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1076-478_1076-457d others(24): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 44906466 | |||||
chr3:44906519
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1076-430A>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906519 | ||||||
chr3:44906542
|
A | G | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-407A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906542 | ||||||
chr3:44906562
|
A | C | 1 | a0004c0004t0001g0242 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1076-387A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 9/13 | chr3 | 44906562 | ||||||
chr3:44907278
|
G | A | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+78G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907278 | ||||||
chr3:44907308
|
A | G | 1 | a0002c0002t0002g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1327+108A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907308 | ||||||
chr3:44907310
|
C | CA | 6 | a0002c0002t0002g0022a0002c0002t0002g0063a0002c0002t0002g0092others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327+133dupA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | |||||
chr3:44907310
|
CA | C | 6 | a0002c0002t0002g0064a0002c0002t0002g0076a0002c0002t0002g0143others(3): Show | 6 | HG00408.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327+133delA | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | |||||
chr3:44907310
|
CAA | C | 15 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0164others(12): Show | 15 | HG00741.hp1 HG01361.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1327+132_1327+133d others(4): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | |||||
chr3:44907310
|
CAAA | C | 81 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1327+131_1327+133d others(5): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | |||||
chr3:44907310
|
CAAAA | C | 106 | a0001c0001t0001g0130a0001c0001t0001g0209a0001c0001t0001g0227others(103): Show | 113 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.1327+130_1327+133d others(6): Show |
TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44907310 | |||||
chr3:44907412
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1327+212G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907412 | ||||||
chr3:44907561
|
T | G | 215 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1327+361T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907561 | ||||||
chr3:44907618
|
G | A | 1 | a0019c0022t0001g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1327+418G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907618 | ||||||
chr3:44907847
|
T | C | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+647T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907847 | ||||||
chr3:44907866
|
T | C | 1 | a0002c0002t0002g0022 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1327+666T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44907866 | ||||||
chr3:44908000
|
A | G | 21 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(18): Show | 23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1327+800A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908000 | ||||||
chr3:44908244
|
C | G | 21 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(18): Show | 23 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1327+1044C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908244 | ||||||
chr3:44908374
|
G | GT | 24 | a0002c0002t0002g0063a0006c0010t0003g0006a0006c0010t0003g0037others(21): Show | 26 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327+1183dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908374 | |||||
chr3:44908375
|
T | G | 2 | a0003c0003t0001g0072a0022c0026t0006g0229 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1327+1175T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908375 | ||||||
chr3:44908413
|
G | GT | 29 | a0002c0002t0002g0086a0006c0010t0003g0006a0006c0010t0003g0037others(26): Show | 31 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1327+1221dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908413 | |||||
chr3:44908430
|
A | C | 27 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(24): Show | 29 | HG01884.hp2 HG02056.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1327+1230A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908430 | ||||||
chr3:44908503
|
G | T | 4 | a0008c0007t0001g0033a0008c0007t0001g0034a0016c0020t0001g0029others(1): Show | 4 | HG01109.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327+1303G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908503 | ||||||
chr3:44908534
|
T | G | 1 | a0011c0011t0001g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1327+1334T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908534 | ||||||
chr3:44908572
|
A | AT | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+1373dupT | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 44908572 | |||||
chr3:44908574
|
A | C | 178 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1327+1374A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908574 | ||||||
chr3:44908724
|
C | T | 79 | a0001c0001t0001g0130a0001c0001t0001g0195a0001c0001t0001g0205others(76): Show | 84 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1328-1366C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908724 | ||||||
chr3:44908757
|
C | T | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1328-1333C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908757 | ||||||
chr3:44908809
|
T | G | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1328-1281T>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908809 | ||||||
chr3:44908835
|
C | T | 2 | a0002c0002t0002g0274a0002c0002t0002g0275 | 2 | HG00280.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1328-1255C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908835 | ||||||
chr3:44908873
|
G | A | 1 | a0006c0010t0003g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1328-1217G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44908873 | ||||||
chr3:44909008
|
A | G | 206 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1328-1082A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909008 | ||||||
chr3:44909403
|
A | G | 215 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1328-687A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909403 | ||||||
chr3:44909682
|
C | G | 200 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(197): Show | 213 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1328-408C>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909682 | ||||||
chr3:44909911
|
G | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1328-179G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909911 | ||||||
chr3:44909942
|
A | G | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1328-148A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 10/13 | chr3 | 44909942 | ||||||
chr3:44910439
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1606+71T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910439 | ||||||
chr3:44910473
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0182 | 3 | NA18952.hp2 NA19001.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1606+105G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910473 | ||||||
chr3:44910551
|
A | G | 215 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1606+183A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910551 | ||||||
chr3:44910574
|
G | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1606+206G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910574 | ||||||
chr3:44910698
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1607-260A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910698 | ||||||
chr3:44910768
|
T | C | 6 | a0009c0008t0004g0157a0009c0008t0004g0165a0009c0008t0004g0179others(3): Show | 6 | NA18975.hp1 NA18984.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1607-190T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910768 | ||||||
chr3:44910813
|
T | C | 2 | a0003c0003t0001g0060a0003c0003t0001g0061 | 2 | HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1607-145T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910813 | ||||||
chr3:44910915
|
G | C | 205 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(202): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1607-43G>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 11/13 | chr3 | 44910915 | ||||||
chr3:44911165
|
T | A | 1 | a0007c0006t0003g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1776+38T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 12/13 | chr3 | 44911165 | ||||||
chr3:44911188
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1776+61C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 12/13 | chr3 | 44911188 | ||||||
chr3:44911446
|
A | G | 9 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1913+40A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911446 | ||||||
chr3:44911450
|
A | C | 206 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1913+44A>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911450 | ||||||
chr3:44911548
|
G | T | 3 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168 | 3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1913+142G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911548 | ||||||
chr3:44911643
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1913+237G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911643 | ||||||
chr3:44911834
|
C | T | 215 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 228 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1913+428C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44911834 | ||||||
chr3:44912006
|
T | C | 1 | a0002c0002t0010g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1913+600T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912006 | ||||||
chr3:44912010
|
T | C | 1 | a0024c0028t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1913+604T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912010 | ||||||
chr3:44912034
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1913+628T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912034 | ||||||
chr3:44912245
|
C | T | 3 | a0011c0011t0001g0025a0011c0011t0001g0026a0011c0011t0001g0027 | 3 | HG02809.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1913+839C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912245 | ||||||
chr3:44912429
|
G | T | 1 | a0004c0004t0001g0246 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1913+1023G>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912429 | ||||||
chr3:44912482
|
A | G | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1913+1076A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912482 | ||||||
chr3:44912548
|
T | C | 4 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-1036T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912548 | ||||||
chr3:44912710
|
T | C | 4 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-874T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912710 | ||||||
chr3:44912798
|
C | T | 6 | a0011c0011t0001g0023a0011c0011t0001g0025a0011c0011t0001g0026others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1914-786C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912798 | ||||||
chr3:44912894
|
T | C | 1 | a0002c0018t0002g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1914-690T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912894 | ||||||
chr3:44912923
|
T | A | 10 | a0006c0010t0003g0006a0006c0010t0003g0037a0006c0010t0003g0053others(7): Show | 12 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1914-661T>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912923 | ||||||
chr3:44912986
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0196a0001c0001t0001g0240 | 3 | HG00733.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1914-598C>T | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912986 | ||||||
chr3:44912989
|
A | G | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1914-595A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44912989 | ||||||
chr3:44913017
|
A | G | 10 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(7): Show | 10 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1914-567A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913017 | ||||||
chr3:44913065
|
G | A | 2 | a0001c0014t0001g0015a0001c0014t0001g0226 | 3 | HG02071.hp1 HG02129.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1914-519G>A | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913065 | ||||||
chr3:44913152
|
A | G | 4 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-432A>G | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913152 | ||||||
chr3:44913564
|
T | C | 4 | a0002c0013t0006g0156a0002c0013t0006g0158a0002c0013t0006g0168others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914-20T>C | TGM4 | ENSG00000163810.13 | transcript | ENST00000296125.9 | protein_coding | 13/13 | chr3 | 44913564 |