geneid | 29767 |
---|---|
ensemblid | ENSG00000128872.10 |
hgncid | 11872 |
symbol | TMOD2 |
name | tropomodulin 2 |
refseq_nuc | NM_014548.4 |
refseq_prot | NP_055363.1 |
ensembl_nuc | ENST00000249700.9 |
ensembl_prot | ENSP00000249700.4 |
mane_status | MANE Select |
chr | chr15 |
start | 51751597 |
end | 51816363 |
strand | + |
ver | v1.2 |
region | chr15:51751597-51816363 |
region5000 | chr15:51746597-51821363 |
regionname0 | TMOD2_chr15_51751597_51816363 |
regionname5000 | TMOD2_chr15_51746597_51821363 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 351 | 367 | 90 | 67 | 162 | 10 | 36 | 138 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0002 | 0/0 | 351 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0003 | 0/0 | 351 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1056 | 366 | 90 | 67 | 161 | 10 | 36 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
c0002 | 0/0 | 1056 | 5 | 0 | 5 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
c0003 | 0/0 | 1056 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
c0004 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8095 | 81 | 20 | 8 | 46 | 0 | 7 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0002 | 0/0 | 8096 | 62 | 12 | 8 | 38 | 2 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0003 | 1/0 | 8095 | 31 | 2 | 16 | 0 | 3 | 9 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0004 | 0/1 | 8095 | 25 | 2 | 13 | 1 | 3 | 5 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0005 | 0/0 | 8096 | 25 | 0 | 9 | 15 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0006 | 0/0 | 8096 | 19 | 0 | 1 | 18 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0007 | 0/0 | 8095 | 19 | 18 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0008 | 0/0 | 8095 | 11 | 0 | 0 | 5 | 0 | 6 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0009 | 0/0 | 8096 | 9 | 0 | 0 | 7 | 1 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0010 | 0/0 | 8095 | 8 | 7 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0011 | 0/0 | 8095 | 7 | 0 | 0 | 7 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0012 | 0/0 | 8096 | 7 | 7 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0013 | 0/0 | 8096 | 5 | 0 | 0 | 4 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0014 | 0/0 | 8095 | 4 | 0 | 0 | 4 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0015 | 0/0 | 8095 | 4 | 0 | 3 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0016 | 0/0 | 8096 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0017 | 0/0 | 8096 | 3 | 1 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0018 | 0/0 | 8095 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0019 | 0/0 | 8095 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0020 | 0/0 | 8096 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0021 | 0/0 | 8096 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0022 | 0/0 | 8095 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0023 | 0/0 | 8096 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0024 | 0/0 | 8083 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0025 | 0/0 | 8095 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0026 | 0/0 | 8095 | 2 | 0 | 1 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0027 | 0/0 | 8095 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0028 | 0/0 | 8096 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0029 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0030 | 0/0 | 8095 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0031 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0032 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0033 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0034 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0035 | 0/0 | 8096 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0036 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0037 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0038 | 0/0 | 8096 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0039 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0040 | 0/0 | 8095 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0041 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0042 | 0/0 | 8094 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0043 | 0/0 | 8095 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0044 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0045 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0046 | 0/0 | 8095 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0047 | 0/0 | 8095 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0048 | 0/0 | 8095 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0049 | 0/0 | 8094 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0050 | 0/0 | 8095 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0051 | 0/0 | 8094 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0052 | 0/0 | 8095 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0053 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0054 | 0/0 | 8096 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0055 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
t0056 | 0/0 | 8096 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1056 | 366 | 90 | 67 | 161 | 10 | 36 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0004 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0002c0002 | 0/0 | 1056 | 5 | 0 | 5 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0003c0003 | 0/0 | 1056 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9150 | 81 | 20 | 8 | 46 | 0 | 7 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0002 | 0/0 | 9151 | 61 | 12 | 8 | 37 | 2 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0003 | 1/0 | 9150 | 29 | 2 | 16 | 0 | 3 | 7 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0004 | 0/1 | 9150 | 20 | 2 | 8 | 1 | 3 | 5 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0005 | 0/0 | 9151 | 25 | 0 | 9 | 15 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0006 | 0/0 | 9151 | 19 | 0 | 1 | 18 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0007 | 0/0 | 9150 | 19 | 18 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0008 | 0/0 | 9150 | 11 | 0 | 0 | 5 | 0 | 6 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0009 | 0/0 | 9151 | 9 | 0 | 0 | 7 | 1 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0010 | 0/0 | 9150 | 8 | 7 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0011 | 0/0 | 9150 | 7 | 0 | 0 | 7 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0012 | 0/0 | 9151 | 7 | 7 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0013 | 0/0 | 9151 | 5 | 0 | 0 | 4 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0014 | 0/0 | 9150 | 4 | 0 | 0 | 4 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0015 | 0/0 | 9150 | 4 | 0 | 3 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0016 | 0/0 | 9151 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0017 | 0/0 | 9151 | 3 | 1 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0018 | 0/0 | 9150 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0019 | 0/0 | 9150 | 3 | 3 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0020 | 0/0 | 9151 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0021 | 0/0 | 9151 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0022 | 0/0 | 9150 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0023 | 0/0 | 9151 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0024 | 0/0 | 9138 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0025 | 0/0 | 9150 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0026 | 0/0 | 9150 | 2 | 0 | 1 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0027 | 0/0 | 9150 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0028 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0029 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0030 | 0/0 | 9150 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0031 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0032 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0033 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0034 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0035 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0036 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0037 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0038 | 0/0 | 9151 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0039 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0040 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0041 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0042 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0043 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0044 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0045 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0046 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0047 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0048 | 0/0 | 9150 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0049 | 0/0 | 9149 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0050 | 0/0 | 9150 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0051 | 0/0 | 9149 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0052 | 0/0 | 9150 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0053 | 0/0 | 9151 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0054 | 0/0 | 9151 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0055 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0001t0056 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0001c0004t0002 | 0/0 | 9151 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0002c0002t0004 | 0/0 | 9150 | 5 | 0 | 5 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
a0003c0003t0003 | 0/0 | 9150 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | copy fasta | chr15 | 51746597 | 51821363 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0008g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0011g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0013g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0013g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0014g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0014g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0015g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0015g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0015g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0015g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0017g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0018g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0018g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0018g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0020g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0021g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0022g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0023g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0024g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0025g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0025g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0026g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0026g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0027g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0028g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0029g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0030g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0031g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0032g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0033g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0034g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0035g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0036g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0037g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0038g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0039g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0040g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0041g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0042g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0043g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0044g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0045g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0046g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0047g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0048g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0049g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0050g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0051g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0052g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0053g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0054g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0055g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0001t0056g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0001c0004t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0002c0002t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0002c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
a0003c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0004 | g0059 | EUR | GBR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0164 | EUR | GBR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0232 | EUR | FIN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00408 | hp1 | a0001 | c0001 | t0011 | g0334 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00609 | hp2 | a0001 | c0001 | t0021 | g0090 | EAS | CHS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG00741 | hp2 | a0001 | c0001 | t0035 | g0018 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0239 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01167 | hp1 | a0001 | c0001 | t0017 | g0004 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01169 | hp2 | a0001 | c0001 | t0017 | g0004 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0008 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0227 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01256 | hp2 | a0001 | c0001 | t0020 | g0057 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01257 | hp2 | a0001 | c0001 | t0027 | g0014 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01258 | hp1 | a0001 | c0001 | t0020 | g0113 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01258 | hp2 | a0001 | c0001 | t0027 | g0014 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01358 | hp2 | a0001 | c0001 | t0026 | g0253 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01496 | hp2 | a0001 | c0001 | t0028 | g0078 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0049 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01515 | hp2 | a0001 | c0001 | t0015 | g0217 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0104 | EUR | IBS | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01884 | hp1 | a0001 | c0001 | t0034 | g0114 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0197 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01928 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0181 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01943 | hp1 | a0001 | c0001 | t0052 | g0196 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0064 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0179 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01978 | hp1 | a0001 | c0001 | t0054 | g0199 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0218 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01993 | hp1 | a0002 | c0002 | t0004 | g0065 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02027 | hp2 | a0001 | c0001 | t0021 | g0047 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0048 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02145 | hp2 | a0001 | c0001 | t0016 | g0140 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CDX | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02273 | hp1 | a0002 | c0002 | t0004 | g0061 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02273 | hp2 | a0001 | c0001 | t0025 | g0352 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0135 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02602 | hp2 | a0001 | c0001 | t0048 | g0271 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0224 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0121 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02738 | hp1 | a0001 | c0001 | t0008 | g0203 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0221 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0119 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02895 | hp2 | a0001 | c0001 | t0024 | g0009 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0223 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02897 | hp2 | a0001 | c0001 | t0024 | g0009 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02922 | hp2 | a0001 | c0001 | t0017 | g0149 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0238 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02970 | hp2 | a0001 | c0001 | t0018 | g0265 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03041 | hp1 | a0001 | c0001 | t0018 | g0266 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03098 | hp2 | a0001 | c0001 | t0019 | g0208 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03130 | hp2 | a0001 | c0001 | t0049 | g0276 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03195 | hp2 | a0001 | c0001 | t0031 | g0079 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0209 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0141 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0120 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03486 | hp2 | a0001 | c0001 | t0053 | g0176 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03490 | hp1 | a0003 | c0003 | t0003 | g0015 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03490 | hp2 | a0001 | c0001 | t0051 | g0335 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03491 | hp2 | a0001 | c0001 | t0026 | g0252 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03492 | hp2 | a0003 | c0003 | t0003 | g0015 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0220 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03540 | hp1 | a0001 | c0001 | t0018 | g0264 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | GWD | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0132 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0142 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0275 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0260 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03704 | hp2 | a0001 | c0001 | t0030 | g0060 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0355 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04115 | hp1 | a0001 | c0001 | t0013 | g0147 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0278 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | BEB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04199 | hp2 | a0001 | c0001 | t0023 | g0251 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04204 | hp1 | a0001 | c0001 | t0038 | g0038 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0268 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | STU | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0215 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18747 | hp1 | a0001 | c0001 | t0013 | g0146 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | CHB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18906 | hp1 | a0001 | c0001 | t0037 | g0023 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0237 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18939 | hp1 | a0001 | c0001 | t0014 | g0287 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18940 | hp1 | a0001 | c0001 | t0011 | g0288 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18945 | hp2 | a0001 | c0001 | t0014 | g0321 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18946 | hp1 | a0001 | c0001 | t0029 | g0026 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18946 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18954 | hp2 | a0001 | c0001 | t0047 | g0282 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18957 | hp1 | a0001 | c0001 | t0009 | g0166 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18960 | hp1 | a0001 | c0001 | t0045 | g0167 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18960 | hp2 | a0001 | c0001 | t0011 | g0304 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0305 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18967 | hp2 | a0001 | c0001 | t0014 | g0325 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18971 | hp1 | a0001 | c0001 | t0013 | g0143 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18971 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18977 | hp2 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18978 | hp1 | a0001 | c0001 | t0009 | g0172 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18979 | hp2 | a0001 | c0001 | t0050 | g0301 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18980 | hp2 | a0001 | c0001 | t0025 | g0353 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18982 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18987 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18992 | hp1 | a0001 | c0001 | t0013 | g0148 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18992 | hp2 | a0001 | c0001 | t0008 | g0269 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18993 | hp1 | a0001 | c0001 | t0011 | g0306 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18993 | hp2 | a0001 | c0001 | t0044 | g0168 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18999 | hp1 | a0001 | c0001 | t0032 | g0092 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19002 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19004 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19007 | hp1 | a0001 | c0001 | t0023 | g0333 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19007 | hp2 | a0001 | c0001 | t0056 | g0144 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19010 | hp1 | a0001 | c0001 | t0055 | g0178 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19011 | hp1 | a0001 | c0001 | t0046 | g0270 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19012 | hp1 | a0001 | c0001 | t0041 | g0028 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19012 | hp2 | a0001 | c0001 | t0014 | g0316 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19030 | hp1 | a0001 | c0001 | t0022 | g0277 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0226 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0205 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19056 | hp1 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19058 | hp1 | a0001 | c0001 | t0039 | g0109 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19058 | hp2 | a0001 | c0001 | t0011 | g0307 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19078 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19080 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19081 | hp2 | a0001 | c0001 | t0040 | g0030 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19086 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19086 | hp2 | a0001 | c0001 | t0043 | g0290 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0136 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA19240 | hp2 | a0001 | c0001 | t0042 | g0117 | AFR | YRI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ASW | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0066 | EUR | TSI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | GIH | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20905 | hp2 | a0001 | c0001 | t0009 | g0165 | SAS | GIH | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01123 | hp1 | a0001 | c0001 | t0015 | g0216 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02486 | hp1 | a0001 | c0001 | t0019 | g0204 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02559 | hp1 | a0001 | c0001 | t0036 | g0116 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | MSL | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20300 | hp1 | a0001 | c0001 | t0022 | g0262 | AFR | USA | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA20300 | hp2 | a0001 | c0001 | t0033 | g0002 | AFR | USA | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0137 | AFR | LWK | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0071 | REF | REF | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0163 | REF | REF | TMOD2_chr15_51746597_51821363 | TMOD2 | chr15 | 51746597 | 51821363 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51766485
|
T | C | 1 | a0003 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.44T>C | p.Ile15Thr | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/10 | 229/9150 | 44/1056 | 15/351 | chr15 | 51766485 | ||
chr15:51768322
|
C | G | 1 | a0002 | 5 | HG01928.hp2 HG01943.hp2 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.187C>G | p.Pro63Ala | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/10 | 372/9150 | 187/1056 | 63/351 | chr15 | 51768322 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51776942
|
A | T | 1 | a0001c0004 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.417A>T | p.Gly139Gly | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/10 | 602/9150 | 417/1056 | 139/351 | chr15 | 51776942 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51751680
|
G | A | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(20): Show | 133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-102G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/10 | 14762 | chr15 | 51751680 | |||||
chr15:51766439
|
G | A | 1 | a0001c0001t0043 | 1 | NA19086.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/10 | 3 | chr15 | 51766439 | |||||
chr15:51808707
|
G | A | 3 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*253G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 253 | chr15 | 51808707 | |||||
chr15:51808738
|
T | C | 1 | a0001c0001t0022 | 2 | NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*284T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 284 | chr15 | 51808738 | |||||
chr15:51809148
|
T | G | 1 | a0001c0001t0014 | 4 | NA18939.hp1 NA18945.hp2 NA18967.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*694T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 694 | chr15 | 51809148 | |||||
chr15:51809176
|
C | A | 1 | a0001c0001t0028 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 722 | chr15 | 51809176 | |||||
chr15:51809188
|
T | C | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 734 | chr15 | 51809188 | |||||
chr15:51809397
|
T | A | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(48): Show | 306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*943T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 943 | chr15 | 51809397 | |||||
chr15:51809596
|
A | T | 2 | a0001c0001t0040a0001c0001t0041 | 2 | NA19012.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1142A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1142 | chr15 | 51809596 | |||||
chr15:51809728
|
TCCTTTCT others(6): Show |
T | 1 | a0001c0001t0024 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1282_*1294delCCCC others(9): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1282 | INFO_REALIGN_3_PRIME | chr15 | 51809728 | ||||
chr15:51809832
|
C | T | 1 | a0001c0001t0026 | 2 | HG01358.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1378 | chr15 | 51809832 | |||||
chr15:51809876
|
T | A | 1 | a0001c0001t0029 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1422T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1422 | chr15 | 51809876 | |||||
chr15:51809957
|
T | C | 1 | a0001c0001t0019 | 3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1503 | chr15 | 51809957 | |||||
chr15:51810059
|
C | A | 3 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1605C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1605 | chr15 | 51810059 | |||||
chr15:51810133
|
G | GT | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1682dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1683 | INFO_REALIGN_3_PRIME | chr15 | 51810133 | ||||
chr15:51810223
|
T | C | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1769 | chr15 | 51810223 | |||||
chr15:51810434
|
G | A | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1980G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 1980 | chr15 | 51810434 | |||||
chr15:51810485
|
A | G | 1 | a0001c0001t0039 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2031A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2031 | chr15 | 51810485 | |||||
chr15:51810533
|
A | G | 1 | a0001c0001t0051 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2079 | chr15 | 51810533 | |||||
chr15:51810550
|
C | T | 1 | a0001c0001t0024 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2096C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2096 | chr15 | 51810550 | |||||
chr15:51810556
|
C | G | 1 | a0001c0001t0050 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2102C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2102 | chr15 | 51810556 | |||||
chr15:51810567
|
G | C | 2 | a0001c0001t0016a0001c0001t0024 | 5 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2113G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2113 | chr15 | 51810567 | |||||
chr15:51810635
|
T | G | 14 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(11): Show | 118 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2181T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2181 | chr15 | 51810635 | |||||
chr15:51810750
|
CT | C | 8 | a0001c0001t0004a0001c0001t0030a0001c0001t0040others(5): Show | 31 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2313delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2313 | INFO_REALIGN_3_PRIME | chr15 | 51810750 | ||||
chr15:51810772
|
C | G | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2318C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2318 | chr15 | 51810772 | |||||
chr15:51810842
|
G | A | 1 | a0001c0001t0027 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2388G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2388 | chr15 | 51810842 | |||||
chr15:51810896
|
G | A | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2442G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2442 | chr15 | 51810896 | |||||
chr15:51810940
|
T | C | 5 | a0001c0001t0005a0001c0001t0052a0001c0001t0053others(2): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2486T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2486 | chr15 | 51810940 | |||||
chr15:51810984
|
G | A | 2 | a0001c0001t0025a0001c0001t0046 | 3 | HG02273.hp2 NA18980.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2530G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2530 | chr15 | 51810984 | |||||
chr15:51811224
|
G | A | 1 | a0001c0001t0053 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2770 | chr15 | 51811224 | |||||
chr15:51811323
|
G | C | 4 | a0001c0001t0005a0001c0001t0052a0001c0001t0054others(1): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2869G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 2869 | chr15 | 51811323 | |||||
chr15:51811622
|
C | A | 35 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(32): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*3168C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3168 | chr15 | 51811622 | |||||
chr15:51811662
|
C | T | 3 | a0001c0001t0005a0001c0001t0052a0001c0001t0054 | 27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3208C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3208 | chr15 | 51811662 | |||||
chr15:51811860
|
G | A | 1 | a0001c0001t0031 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3406G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3406 | chr15 | 51811860 | |||||
chr15:51812103
|
C | G | 1 | a0001c0001t0029 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 3649 | chr15 | 51812103 | |||||
chr15:51812463
|
A | C | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4009A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4009 | chr15 | 51812463 | |||||
chr15:51813042
|
A | G | 1 | a0001c0001t0011 | 7 | HG00408.hp1 NA18940.hp1 NA18960.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4588A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4588 | chr15 | 51813042 | |||||
chr15:51813052
|
G | T | 1 | a0001c0001t0054 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4598G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4598 | chr15 | 51813052 | |||||
chr15:51813085
|
A | C | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(47): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*4631A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4631 | chr15 | 51813085 | |||||
chr15:51813238
|
C | T | 1 | a0001c0001t0018 | 3 | HG02970.hp2 HG03041.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4784C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4784 | chr15 | 51813238 | |||||
chr15:51813419
|
A | G | 7 | a0001c0001t0006a0001c0001t0029a0001c0001t0036others(4): Show | 25 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4965A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 4965 | chr15 | 51813419 | |||||
chr15:51813466
|
T | C | 1 | a0001c0001t0047 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5012T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5012 | chr15 | 51813466 | |||||
chr15:51813515
|
G | A | 1 | a0001c0001t0032 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5061G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5061 | chr15 | 51813515 | |||||
chr15:51813558
|
C | A | 1 | a0001c0001t0040 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5104C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5104 | chr15 | 51813558 | |||||
chr15:51813688
|
G | T | 1 | a0001c0001t0017 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5234G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5234 | chr15 | 51813688 | |||||
chr15:51813804
|
G | A | 1 | a0001c0001t0033 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5350G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5350 | chr15 | 51813804 | |||||
chr15:51813817
|
A | G | 1 | a0001c0001t0021 | 2 | HG00609.hp2 HG02027.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5363A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5363 | chr15 | 51813817 | |||||
chr15:51813832
|
C | T | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5378 | chr15 | 51813832 | |||||
chr15:51813995
|
A | T | 1 | a0001c0001t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5541A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5541 | chr15 | 51813995 | |||||
chr15:51814104
|
G | A | 33 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(30): Show | 185 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*5650G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5650 | chr15 | 51814104 | |||||
chr15:51814172
|
G | C | 1 | a0001c0001t0020 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5718G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5718 | chr15 | 51814172 | |||||
chr15:51814287
|
C | T | 1 | a0001c0001t0034 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5833C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5833 | chr15 | 51814287 | |||||
chr15:51814436
|
T | G | 1 | a0001c0001t0032 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5982T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 5982 | chr15 | 51814436 | |||||
chr15:51814498
|
T | G | 1 | a0001c0001t0016 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6044T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6044 | chr15 | 51814498 | |||||
chr15:51814560
|
G | A | 1 | a0001c0001t0044 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6106G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6106 | chr15 | 51814560 | |||||
chr15:51814792
|
G | A | 2 | a0001c0001t0013a0001c0001t0056 | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6338G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6338 | chr15 | 51814792 | |||||
chr15:51814857
|
A | G | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0020others(13): Show | 102 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*6403A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6403 | chr15 | 51814857 | |||||
chr15:51814864
|
G | A | 1 | a0001c0001t0015 | 4 | HG01081.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6410G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6410 | chr15 | 51814864 | |||||
chr15:51814882
|
C | T | 1 | a0001c0001t0045 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6428C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6428 | chr15 | 51814882 | |||||
chr15:51814926
|
G | A | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(52): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*6472G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6472 | chr15 | 51814926 | |||||
chr15:51814940
|
G | A | 1 | a0001c0001t0013 | 5 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6486G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6486 | chr15 | 51814940 | |||||
chr15:51815051
|
C | T | 1 | a0001c0001t0048 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6597C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6597 | chr15 | 51815051 | |||||
chr15:51815089
|
C | G | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6635C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6635 | chr15 | 51815089 | |||||
chr15:51815396
|
T | G | 1 | a0001c0001t0012 | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6942T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 6942 | chr15 | 51815396 | |||||
chr15:51815501
|
C | T | 1 | a0001c0001t0042 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7047C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 7047 | chr15 | 51815501 | |||||
chr15:51815534
|
C | T | 5 | a0001c0001t0006a0001c0001t0029a0001c0001t0038others(2): Show | 23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7080C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 10/10 | 7080 | chr15 | 51815534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51751866
|
G | A | 1 | a0001c0001t0012g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-70+154G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51751866 | ||||||
chr15:51752061
|
C | T | 158 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(155): Show | 165 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.-70+349C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752061 | ||||||
chr15:51752118
|
G | T | 1 | a0001c0001t0008g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-70+406G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752118 | ||||||
chr15:51752171
|
G | A | 1 | a0001c0001t0017g0004 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-70+459G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752171 | ||||||
chr15:51752429
|
C | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+717C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752429 | ||||||
chr15:51752490
|
A | G | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-70+778A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752490 | ||||||
chr15:51752581
|
C | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+869C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752581 | ||||||
chr15:51752737
|
A | C | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+1025A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752737 | ||||||
chr15:51752821
|
A | T | 3 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | HG02074.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-70+1109A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752821 | ||||||
chr15:51752824
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+1112G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752824 | ||||||
chr15:51752905
|
A | G | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70+1193A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752905 | ||||||
chr15:51752918
|
G | A | 52 | a0001c0001t0003g0003a0001c0001t0003g0210a0001c0001t0003g0211others(49): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-70+1206G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51752918 | ||||||
chr15:51753083
|
G | A | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-70+1371G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753083 | ||||||
chr15:51753105
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70+1393G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753105 | ||||||
chr15:51753153
|
T | A | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-70+1441T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753153 | ||||||
chr15:51753171
|
G | A | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-70+1459G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753171 | ||||||
chr15:51753190
|
A | G | 1 | a0001c0001t0005g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-70+1478A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753190 | ||||||
chr15:51753445
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18943.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-70+1733A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753445 | ||||||
chr15:51753451
|
C | T | 51 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(48): Show | 55 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.-70+1739C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753451 | ||||||
chr15:51753552
|
A | C | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+1840A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753552 | ||||||
chr15:51753605
|
G | T | 1 | a0001c0001t0008g0355 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-70+1893G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753605 | ||||||
chr15:51753606
|
C | T | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+1894C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753606 | ||||||
chr15:51753705
|
A | G | 1 | a0001c0001t0005g0201 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-70+1993A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753705 | ||||||
chr15:51753776
|
TA | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+2065delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753776 | ||||||
chr15:51753831
|
T | C | 1 | a0001c0001t0035g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-70+2119T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753831 | ||||||
chr15:51753959
|
G | A | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-70+2247G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51753959 | ||||||
chr15:51754012
|
C | T | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+2300C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754012 | ||||||
chr15:51754052
|
G | T | 77 | a0001c0001t0001g0016a0001c0001t0001g0279a0001c0001t0001g0280others(74): Show | 78 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-70+2340G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754052 | ||||||
chr15:51754162
|
T | C | 343 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(340): Show | 360 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.-70+2450T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754162 | ||||||
chr15:51754168
|
C | T | 2 | a0001c0001t0003g0249a0001c0001t0003g0250 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-70+2456C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754168 | ||||||
chr15:51754298
|
G | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+2586G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754298 | ||||||
chr15:51754473
|
C | T | 50 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(47): Show | 54 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.-70+2761C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754473 | ||||||
chr15:51754516
|
A | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+2804A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754516 | ||||||
chr15:51754660
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-70+2948A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754660 | ||||||
chr15:51754661
|
C | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+2949C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754661 | ||||||
chr15:51754706
|
A | T | 1 | a0001c0001t0008g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70+2994A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754706 | ||||||
chr15:51754875
|
A | G | 1 | a0001c0001t0006g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-70+3163A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754875 | ||||||
chr15:51754956
|
G | A | 1 | a0001c0001t0037g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-70+3244G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51754956 | ||||||
chr15:51755042
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-70+3330T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755042 | ||||||
chr15:51755080
|
T | A | 1 | a0001c0001t0023g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-70+3368T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755080 | ||||||
chr15:51755233
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-70+3521A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755233 | ||||||
chr15:51755240
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+3528G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755240 | ||||||
chr15:51755609
|
G | T | 2 | a0001c0001t0009g0170a0001c0001t0009g0171 | 2 | NA18982.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-70+3897G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755609 | ||||||
chr15:51755782
|
A | G | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+4070A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755782 | ||||||
chr15:51755895
|
T | C | 3 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0047g0282 | 3 | HG02129.hp2 NA18954.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-70+4183T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755895 | ||||||
chr15:51755932
|
G | A | 23 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(20): Show | 24 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-70+4220G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755932 | ||||||
chr15:51755977
|
A | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+4265A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51755977 | ||||||
chr15:51756054
|
C | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+4342C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756054 | ||||||
chr15:51756128
|
C | T | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4416C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756128 | ||||||
chr15:51756129
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+4417C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756129 | ||||||
chr15:51756209
|
G | A | 31 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.-70+4497G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756209 | ||||||
chr15:51756270
|
T | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70+4558T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756270 | ||||||
chr15:51756320
|
T | G | 1 | a0001c0001t0001g0283 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-70+4608T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756320 | ||||||
chr15:51756379
|
A | C | 1 | a0001c0001t0002g0129 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-70+4667A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756379 | ||||||
chr15:51756457
|
C | G | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4745C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756457 | ||||||
chr15:51756493
|
T | G | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+4781T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756493 | ||||||
chr15:51756513
|
A | G | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-70+4801A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756513 | ||||||
chr15:51756514
|
G | T | 2 | a0001c0001t0025g0352a0001c0001t0025g0353 | 2 | HG02273.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-70+4802G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756514 | ||||||
chr15:51756723
|
G | C | 6 | a0001c0001t0007g0206a0001c0001t0007g0207a0001c0001t0007g0209others(3): Show | 6 | HG02486.hp1 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+5011G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756723 | ||||||
chr15:51756762
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-70+5050G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756762 | ||||||
chr15:51756767
|
A | G | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70+5055A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756767 | ||||||
chr15:51756894
|
A | G | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-70+5182A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51756894 | ||||||
chr15:51757102
|
A | G | 3 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG02155.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-70+5390A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757102 | ||||||
chr15:51757141
|
C | T | 1 | a0001c0001t0001g0348 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-70+5429C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757141 | ||||||
chr15:51757184
|
C | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+5472C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757184 | ||||||
chr15:51757216
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-70+5504A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757216 | ||||||
chr15:51757244
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5532A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757244 | ||||||
chr15:51757350
|
G | A | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70+5638G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757350 | ||||||
chr15:51757383
|
C | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-70+5671C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757383 | ||||||
chr15:51757396
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+5684C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757396 | ||||||
chr15:51757401
|
C | CA | 22 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0285others(19): Show | 23 | HG01109.hp2 HG01123.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.-70+5712dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | |||||
chr15:51757401
|
CA | C | 25 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346others(22): Show | 29 | HG00639.hp1 HG00733.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-70+5712delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | |||||
chr15:51757401
|
CAA | C | 43 | a0001c0001t0002g0044a0001c0001t0002g0046a0001c0001t0004g0045others(40): Show | 46 | HG00544.hp1 HG00741.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.-70+5711_-70+5712d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | |||||
chr15:51757401
|
CAAA | C | 129 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(126): Show | 135 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-70+5710_-70+5712d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51757401 | |||||
chr15:51757581
|
C | A | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-70+5869C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757581 | ||||||
chr15:51757624
|
A | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-70+5912A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757624 | ||||||
chr15:51757696
|
T | C | 1 | a0001c0001t0008g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-70+5984T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757696 | ||||||
chr15:51757840
|
G | A | 2 | a0001c0001t0004g0049a0001c0001t0004g0050 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-70+6128G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757840 | ||||||
chr15:51757894
|
G | A | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-70+6182G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757894 | ||||||
chr15:51757996
|
C | G | 1 | a0001c0001t0008g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70+6284C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51757996 | ||||||
chr15:51758037
|
A | G | 1 | a0001c0001t0007g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-70+6325A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758037 | ||||||
chr15:51758086
|
T | G | 1 | a0001c0001t0056g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-70+6374T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758086 | ||||||
chr15:51758151
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-70+6439G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758151 | ||||||
chr15:51758208
|
A | C | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+6496A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758208 | ||||||
chr15:51758314
|
G | T | 1 | a0001c0001t0001g0343 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-70+6602G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758314 | ||||||
chr15:51758416
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-70+6704G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758416 | ||||||
chr15:51758502
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-70+6790C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758502 | ||||||
chr15:51758699
|
G | C | 1 | a0001c0001t0003g0219 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-70+6987G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758699 | ||||||
chr15:51758714
|
A | T | 1 | a0001c0001t0001g0342 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-70+7002A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758714 | ||||||
chr15:51758797
|
G | A | 1 | a0001c0001t0006g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-70+7085G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758797 | ||||||
chr15:51758830
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+7118G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758830 | ||||||
chr15:51758946
|
G | A | 1 | a0001c0001t0005g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-70+7234G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51758946 | ||||||
chr15:51759038
|
ACT | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128 | 3 | HG01099.hp1 HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-70+7329_-70+7330d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51759038 | |||||
chr15:51759058
|
A | T | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-7315A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759058 | ||||||
chr15:51759199
|
GT | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-69-7172delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51759199 | |||||
chr15:51759224
|
G | A | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-69-7149G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759224 | ||||||
chr15:51759658
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-69-6715A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759658 | ||||||
chr15:51759702
|
A | C | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-69-6671A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759702 | ||||||
chr15:51759840
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-6533A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759840 | ||||||
chr15:51759902
|
G | T | 4 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(1): Show | 4 | HG00642.hp1 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-6471G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759902 | ||||||
chr15:51759961
|
C | G | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-6412C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51759961 | ||||||
chr15:51760117
|
C | A | 1 | a0001c0001t0019g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-69-6256C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760117 | ||||||
chr15:51760511
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-5862A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760511 | ||||||
chr15:51760621
|
A | G | 52 | a0001c0001t0003g0003a0001c0001t0003g0210a0001c0001t0003g0211others(49): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-69-5752A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760621 | ||||||
chr15:51760628
|
A | G | 2 | a0001c0001t0016g0141a0001c0001t0016g0142 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-5745A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760628 | ||||||
chr15:51760670
|
G | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-5703G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760670 | ||||||
chr15:51760731
|
G | A | 9 | a0001c0001t0007g0013a0001c0001t0007g0220a0001c0001t0007g0221others(6): Show | 10 | HG01255.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-5642G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760731 | ||||||
chr15:51760814
|
G | GA | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(139): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-69-5550dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51760814 | |||||
chr15:51760959
|
C | T | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-69-5414C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51760959 | ||||||
chr15:51761032
|
T | C | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-69-5341T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761032 | ||||||
chr15:51761048
|
G | T | 2 | a0001c0001t0022g0262a0001c0001t0022g0277 | 2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-69-5325G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761048 | ||||||
chr15:51761049
|
G | T | 2 | a0001c0001t0022g0262a0001c0001t0022g0277 | 2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-69-5324G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761049 | ||||||
chr15:51761080
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-69-5293G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761080 | ||||||
chr15:51761193
|
G | A | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-5180G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761193 | ||||||
chr15:51761226
|
CAA | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0336a0001c0001t0001g0337others(2): Show | 6 | HG00544.hp2 HG01934.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-5146_-69-5145d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761226 | ||||||
chr15:51761249
|
G | T | 1 | a0001c0001t0007g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-69-5124G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761249 | ||||||
chr15:51761256
|
ATGT | A | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-69-5113_-69-5111d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761256 | |||||
chr15:51761347
|
T | C | 1 | a0001c0001t0023g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-69-5026T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761347 | ||||||
chr15:51761441
|
T | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4932T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761441 | ||||||
chr15:51761446
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4927G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761446 | ||||||
chr15:51761570
|
G | GA | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-69-4794dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761570 | |||||
chr15:51761876
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-69-4497G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51761876 | ||||||
chr15:51761991
|
C | CA | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-4374dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51761991 | |||||
chr15:51762085
|
C | A | 1 | a0001c0001t0003g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-69-4288C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762085 | ||||||
chr15:51762097
|
C | T | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-4276C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762097 | ||||||
chr15:51762106
|
G | A | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-69-4267G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762106 | ||||||
chr15:51762301
|
A | T | 1 | a0001c0001t0051g0335 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-69-4072A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762301 | ||||||
chr15:51762328
|
G | A | 22 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(19): Show | 23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-4045G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762328 | ||||||
chr15:51762436
|
G | A | 105 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(102): Show | 106 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-69-3937G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762436 | ||||||
chr15:51762445
|
C | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-3928C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762445 | ||||||
chr15:51762648
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-69-3725T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762648 | ||||||
chr15:51762652
|
C | T | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-3721C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762652 | ||||||
chr15:51762678
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-69-3695C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762678 | ||||||
chr15:51762853
|
C | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-3520C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762853 | ||||||
chr15:51762912
|
T | C | 2 | a0001c0001t0006g0025a0001c0001t0029g0026 | 2 | NA18946.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-69-3461T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762912 | ||||||
chr15:51762913
|
G | C | 1 | a0001c0001t0007g0220 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-69-3460G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762913 | ||||||
chr15:51762922
|
C | T | 1 | a0001c0001t0023g0333 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-69-3451C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762922 | ||||||
chr15:51762974
|
T | G | 1 | a0001c0001t0007g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-69-3399T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51762974 | ||||||
chr15:51763053
|
A | G | 1 | a0001c0001t0006g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-69-3320A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763053 | ||||||
chr15:51763060
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-3313G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763060 | ||||||
chr15:51763077
|
G | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-3296G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763077 | ||||||
chr15:51763101
|
AT | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-69-3267delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763101 | |||||
chr15:51763106
|
T | A | 135 | a0001c0001t0001g0285a0001c0001t0002g0001a0001c0001t0002g0002others(132): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-69-3267T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763106 | ||||||
chr15:51763106
|
TA | T | 50 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(47): Show | 54 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.-69-3256delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763106 | |||||
chr15:51763107
|
A | T | 2 | a0001c0001t0008g0275a0001c0001t0023g0251 | 2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-69-3266A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763107 | ||||||
chr15:51763108
|
A | T | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-3265A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763108 | ||||||
chr15:51763131
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-3242G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763131 | ||||||
chr15:51763143
|
TGCCCAGG others(17): Show |
T | 1 | a0001c0001t0001g0347 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-69-3228_-69-3205d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51763143 | |||||
chr15:51763203
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-3170C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763203 | ||||||
chr15:51763205
|
T | C | 1 | a0001c0001t0017g0004 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-69-3168T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763205 | ||||||
chr15:51763272
|
C | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-69-3101C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763272 | ||||||
chr15:51763341
|
A | G | 7 | a0001c0001t0009g0010a0001c0001t0009g0166a0001c0001t0009g0169others(4): Show | 8 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-69-3032A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763341 | ||||||
chr15:51763357
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-69-3016C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763357 | ||||||
chr15:51763388
|
T | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(103): Show | 107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-69-2985T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763388 | ||||||
chr15:51763723
|
T | G | 1 | a0001c0001t0001g0293 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-2650T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763723 | ||||||
chr15:51763736
|
G | T | 44 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(41): Show | 46 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.-69-2637G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763736 | ||||||
chr15:51763837
|
A | G | 1 | a0001c0001t0001g0346 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-69-2536A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763837 | ||||||
chr15:51763974
|
G | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-2399G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51763974 | ||||||
chr15:51764048
|
T | G | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-2325T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764048 | ||||||
chr15:51764049
|
G | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-2324G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764049 | ||||||
chr15:51764085
|
T | TA | 38 | a0001c0001t0002g0044a0001c0001t0005g0011a0001c0001t0005g0177others(35): Show | 40 | HG00544.hp1 HG01106.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.-69-2276dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | |||||
chr15:51764085
|
TA | T | 153 | a0001c0001t0001g0153a0001c0001t0002g0001a0001c0001t0002g0002others(150): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-2276delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | |||||
chr15:51764085
|
TAA | T | 5 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-2277_-69-2276d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51764085 | |||||
chr15:51764178
|
T | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-69-2195T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764178 | ||||||
chr15:51764211
|
A | G | 1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-69-2162A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764211 | ||||||
chr15:51764254
|
T | C | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-69-2119T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764254 | ||||||
chr15:51764266
|
G | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-2107G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764266 | ||||||
chr15:51764343
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-2030A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764343 | ||||||
chr15:51764377
|
G | T | 2 | a0001c0001t0016g0141a0001c0001t0016g0142 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1996G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764377 | ||||||
chr15:51764396
|
A | C | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-1977A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764396 | ||||||
chr15:51764440
|
C | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1933C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764440 | ||||||
chr15:51764484
|
G | A | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1889G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764484 | ||||||
chr15:51764556
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-1817C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764556 | ||||||
chr15:51764701
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-1672T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764701 | ||||||
chr15:51764740
|
G | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-1633G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764740 | ||||||
chr15:51764807
|
T | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-1566T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764807 | ||||||
chr15:51764825
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-69-1548A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51764825 | ||||||
chr15:51765012
|
A | AT | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1351dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 51765012 | |||||
chr15:51765030
|
T | A | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-69-1343T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765030 | ||||||
chr15:51765063
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0130 | 2 | NA19006.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-69-1310T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765063 | ||||||
chr15:51765160
|
C | T | 2 | a0001c0001t0003g0219a0001c0001t0003g0240 | 2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-69-1213C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765160 | ||||||
chr15:51765213
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-69-1160C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765213 | ||||||
chr15:51765255
|
C | A | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-69-1118C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765255 | ||||||
chr15:51765517
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-69-856C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765517 | ||||||
chr15:51765564
|
A | C | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-69-809A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765564 | ||||||
chr15:51765677
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-69-696C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765677 | ||||||
chr15:51765743
|
A | G | 2 | a0001c0001t0004g0049a0001c0001t0004g0050 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-69-630A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765743 | ||||||
chr15:51765772
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-69-601A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765772 | ||||||
chr15:51765897
|
T | C | 1 | a0001c0001t0017g0004 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-69-476T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765897 | ||||||
chr15:51765987
|
A | G | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-386A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765987 | ||||||
chr15:51765988
|
T | C | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-385T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51765988 | ||||||
chr15:51766184
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-69-189A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 1/9 | chr15 | 51766184 | ||||||
chr15:51766747
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+180G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766747 | ||||||
chr15:51766808
|
G | A | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(133): Show | 143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.126+241G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766808 | ||||||
chr15:51766879
|
A | G | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+312A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766879 | ||||||
chr15:51766892
|
T | C | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.126+325T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51766892 | ||||||
chr15:51767031
|
A | AT | 160 | a0001c0001t0001g0341a0001c0001t0001g0346a0001c0001t0002g0001others(157): Show | 168 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.126+478dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767031 | |||||
chr15:51767031
|
A | ATT | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+477_126+478dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767031 | |||||
chr15:51767085
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+518G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767085 | ||||||
chr15:51767214
|
C | T | 29 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(26): Show | 30 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+647C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767214 | ||||||
chr15:51767410
|
G | T | 1 | a0001c0001t0049g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+843G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767410 | ||||||
chr15:51767634
|
TA | T | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(149): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-616delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 51767634 | |||||
chr15:51767769
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.127-493A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767769 | ||||||
chr15:51767788
|
A | T | 6 | a0001c0001t0007g0206a0001c0001t0007g0207a0001c0001t0007g0209others(3): Show | 6 | HG02486.hp1 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-474A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767788 | ||||||
chr15:51767970
|
A | G | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(133): Show | 143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.127-292A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51767970 | ||||||
chr15:51768095
|
T | C | 2 | a0001c0001t0003g0219a0001c0001t0003g0240 | 2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.127-167T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768095 | ||||||
chr15:51768110
|
G | A | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.127-152G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768110 | ||||||
chr15:51768221
|
G | A | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-41G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 2/9 | chr15 | 51768221 | ||||||
chr15:51768460
|
C | CT | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(148): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.283+54dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768460 | |||||
chr15:51768460
|
C | CTTTT | 26 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0180others(23): Show | 27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.283+51_283+54dupTT others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768460 | |||||
chr15:51768601
|
G | A | 24 | a0001c0001t0004g0045a0001c0001t0004g0049a0001c0001t0004g0050others(21): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.283+183G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768601 | ||||||
chr15:51768609
|
A | G | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(133): Show | 143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.283+191A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768609 | ||||||
chr15:51768703
|
T | C | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0018g0264others(2): Show | 5 | HG01109.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+285T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768703 | ||||||
chr15:51768731
|
A | AGATTCAG others(71): Show |
6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+394_283+471dup others(78): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51768731 | |||||
chr15:51768754
|
C | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(133): Show | 143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.283+336C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768754 | ||||||
chr15:51768784
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283+366G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768784 | ||||||
chr15:51768890
|
G | T | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.283+472G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768890 | ||||||
chr15:51768910
|
T | C | 1 | a0001c0001t0003g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.283+492T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768910 | ||||||
chr15:51768927
|
T | C | 343 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(340): Show | 360 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.283+509T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51768927 | ||||||
chr15:51769017
|
T | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+599T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769017 | ||||||
chr15:51769025
|
A | G | 1 | a0001c0001t0035g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283+607A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769025 | ||||||
chr15:51769324
|
A | T | 4 | a0001c0001t0015g0216a0001c0001t0015g0217a0001c0001t0015g0218others(1): Show | 4 | HG01081.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+906A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769324 | ||||||
chr15:51769536
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.283+1118G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769536 | ||||||
chr15:51769622
|
G | T | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+1204G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769622 | ||||||
chr15:51769743
|
A | G | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+1325A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769743 | ||||||
chr15:51769761
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.283+1343G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769761 | ||||||
chr15:51769772
|
C | A | 1 | a0001c0001t0001g0297 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.283+1354C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769772 | ||||||
chr15:51769824
|
A | C | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.283+1406A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769824 | ||||||
chr15:51769898
|
A | G | 1 | a0001c0001t0007g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283+1480A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51769898 | ||||||
chr15:51770313
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+1895T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770313 | ||||||
chr15:51770480
|
C | A | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.283+2062C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770480 | ||||||
chr15:51770487
|
T | C | 1 | a0001c0001t0006g0025 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.283+2069T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770487 | ||||||
chr15:51770510
|
C | T | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+2092C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770510 | ||||||
chr15:51770584
|
C | T | 1 | a0001c0001t0005g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.283+2166C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770584 | ||||||
chr15:51770623
|
A | G | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.283+2205A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770623 | ||||||
chr15:51770851
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.283+2433G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770851 | ||||||
chr15:51770910
|
G | A | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.283+2492G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770910 | ||||||
chr15:51770982
|
T | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+2564T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51770982 | ||||||
chr15:51771139
|
G | A | 1 | a0001c0001t0006g0027 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.284-2573G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771139 | ||||||
chr15:51771242
|
C | T | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.284-2470C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771242 | ||||||
chr15:51771282
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0033g0002 | 3 | HG02451.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.284-2430C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771282 | ||||||
chr15:51771301
|
A | G | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.284-2411A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771301 | ||||||
chr15:51771339
|
C | T | 1 | a0001c0001t0004g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.284-2373C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771339 | ||||||
chr15:51771348
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284-2364A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771348 | ||||||
chr15:51771542
|
C | G | 182 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(179): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.284-2170C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771542 | ||||||
chr15:51771553
|
A | T | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-2159A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771553 | ||||||
chr15:51771928
|
T | A | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.284-1784T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51771928 | ||||||
chr15:51772033
|
T | C | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1679T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772033 | ||||||
chr15:51772089
|
G | A | 16 | a0001c0001t0005g0177a0001c0001t0005g0179a0001c0001t0005g0181others(13): Show | 16 | HG01496.hp1 HG01934.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-1623G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772089 | ||||||
chr15:51772179
|
C | T | 2 | a0001c0001t0004g0049a0001c0001t0004g0050 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.284-1533C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772179 | ||||||
chr15:51772216
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-1496G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772216 | ||||||
chr15:51772219
|
A | C | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-1493A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772219 | ||||||
chr15:51772319
|
G | A | 16 | a0001c0001t0008g0203a0001c0001t0008g0260a0001c0001t0008g0261others(13): Show | 16 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-1393G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772319 | ||||||
chr15:51772480
|
G | A | 253 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(250): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.284-1232G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772480 | ||||||
chr15:51772790
|
G | A | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(84): Show | 91 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.284-922G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51772790 | ||||||
chr15:51773028
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(130): Show | 139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.284-684C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773028 | ||||||
chr15:51773212
|
A | G | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-500A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773212 | ||||||
chr15:51773274
|
A | C | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.284-438A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773274 | ||||||
chr15:51773328
|
C | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.284-384C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773328 | ||||||
chr15:51773435
|
A | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0044others(55): Show | 60 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.284-277A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773435 | ||||||
chr15:51773623
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.284-89A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773623 | ||||||
chr15:51773628
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-84C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | chr15 | 51773628 | ||||||
chr15:51773672
|
C | CA | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.284-39dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 51773672 | |||||
chr15:51773992
|
A | C | 253 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(250): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.406+158A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51773992 | ||||||
chr15:51774015
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406+181G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774015 | ||||||
chr15:51774111
|
G | A | 140 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(137): Show | 148 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.406+277G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774111 | ||||||
chr15:51774124
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.406+290C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774124 | ||||||
chr15:51774281
|
A | G | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+447A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774281 | ||||||
chr15:51774298
|
A | C | 1 | a0001c0001t0002g0112 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.406+464A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774298 | ||||||
chr15:51774306
|
A | T | 1 | a0001c0001t0010g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406+472A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774306 | ||||||
chr15:51774438
|
T | C | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.406+604T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774438 | ||||||
chr15:51774464
|
G | A | 1 | a0001c0001t0012g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.406+630G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774464 | ||||||
chr15:51774594
|
A | G | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+760A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774594 | ||||||
chr15:51774739
|
A | G | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+905A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774739 | ||||||
chr15:51774927
|
A | C | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1093A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774927 | ||||||
chr15:51774954
|
A | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+1120A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51774954 | ||||||
chr15:51775074
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.406+1240C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775074 | ||||||
chr15:51775262
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.406+1428A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775262 | ||||||
chr15:51775288
|
T | C | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.406+1454T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775288 | ||||||
chr15:51775335
|
T | C | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.406+1501T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775335 | ||||||
chr15:51775458
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0044others(48): Show | 53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.407-1474A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775458 | ||||||
chr15:51775563
|
C | CT | 56 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(53): Show | 58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.407-1364dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775563 | |||||
chr15:51775569
|
C | T | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(120): Show | 131 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.407-1363C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775569 | ||||||
chr15:51775570
|
C | CT | 25 | a0001c0001t0001g0162a0001c0001t0001g0329a0001c0001t0001g0330others(22): Show | 27 | HG00544.hp2 HG01433.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-1337dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | |||||
chr15:51775570
|
C | CTT | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(89): Show | 97 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.407-1338_407-1337d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | |||||
chr15:51775570
|
C | CTTT | 16 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(13): Show | 16 | HG00735.hp1 HG01106.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.407-1339_407-1337d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | |||||
chr15:51775570
|
C | T | 57 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.407-1362C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775570 | ||||||
chr15:51775570
|
CT | C | 15 | a0001c0001t0001g0272a0001c0001t0001g0285a0001c0001t0001g0299others(12): Show | 15 | HG00323.hp2 HG00408.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-1337delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 51775570 | |||||
chr15:51775575
|
T | C | 1 | a0001c0001t0028g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.407-1357T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775575 | ||||||
chr15:51775576
|
T | C | 2 | a0001c0001t0012g0133a0001c0001t0012g0134 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.407-1356T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775576 | ||||||
chr15:51775579
|
T | C | 1 | a0001c0001t0016g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-1353T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775579 | ||||||
chr15:51775670
|
G | C | 168 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(165): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.407-1262G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775670 | ||||||
chr15:51775708
|
G | A | 2 | a0001c0001t0003g0210a0001c0001t0003g0213 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.407-1224G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51775708 | ||||||
chr15:51776070
|
G | C | 24 | a0001c0001t0004g0045a0001c0001t0004g0049a0001c0001t0004g0050others(21): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.407-862G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776070 | ||||||
chr15:51776073
|
T | C | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.407-859T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776073 | ||||||
chr15:51776113
|
T | G | 1 | a0001c0001t0016g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.407-819T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776113 | ||||||
chr15:51776117
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407-815C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776117 | ||||||
chr15:51776211
|
A | G | 4 | a0001c0001t0001g0284a0001c0001t0001g0293a0001c0001t0001g0328others(1): Show | 4 | NA18612.hp2 NA18982.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-721A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776211 | ||||||
chr15:51776300
|
G | A | 1 | a0001c0001t0049g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.407-632G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776300 | ||||||
chr15:51776400
|
C | T | 1 | a0001c0001t0005g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.407-532C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776400 | ||||||
chr15:51776416
|
T | C | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.407-516T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776416 | ||||||
chr15:51776677
|
T | C | 135 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(132): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.407-255T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776677 | ||||||
chr15:51776712
|
A | G | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.407-220A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776712 | ||||||
chr15:51776726
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-206A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776726 | ||||||
chr15:51776786
|
T | C | 1 | a0001c0001t0008g0260 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.407-146T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776786 | ||||||
chr15:51776810
|
G | A | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.407-122G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776810 | ||||||
chr15:51776917
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.407-15G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 4/9 | chr15 | 51776917 | ||||||
chr15:51777033
|
A | C | 1 | a0001c0001t0007g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.493+15A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777033 | ||||||
chr15:51777065
|
A | G | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493+47A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777065 | ||||||
chr15:51777081
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.493+63G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777081 | ||||||
chr15:51777096
|
T | C | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493+78T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777096 | ||||||
chr15:51777193
|
G | A | 4 | a0001c0001t0006g0029a0001c0001t0006g0031a0001c0001t0040g0030others(1): Show | 4 | NA18964.hp1 NA19003.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+175G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777193 | ||||||
chr15:51777544
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.493+526T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777544 | ||||||
chr15:51777570
|
C | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0326a0001c0001t0001g0327 | 3 | NA18961.hp2 NA19001.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.493+552C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777570 | ||||||
chr15:51777573
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+555G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777573 | ||||||
chr15:51777638
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+620C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777638 | ||||||
chr15:51777643
|
A | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+625A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777643 | ||||||
chr15:51777747
|
A | G | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.493+729A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51777747 | ||||||
chr15:51778019
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.493+1001T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778019 | ||||||
chr15:51778051
|
G | A | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+1033G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778051 | ||||||
chr15:51778174
|
A | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+1156A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778174 | ||||||
chr15:51778189
|
G | A | 1 | a0001c0001t0006g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.493+1171G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778189 | ||||||
chr15:51778254
|
C | T | 135 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(132): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.493+1236C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778254 | ||||||
chr15:51778323
|
C | G | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.493+1305C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778323 | ||||||
chr15:51778341
|
T | G | 1 | a0001c0001t0050g0301 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.493+1323T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778341 | ||||||
chr15:51778349
|
G | C | 1 | a0001c0001t0003g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.493+1331G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778349 | ||||||
chr15:51778413
|
C | T | 1 | a0001c0001t0028g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.493+1395C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778413 | ||||||
chr15:51778426
|
T | A | 24 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(21): Show | 25 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.493+1408T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778426 | ||||||
chr15:51778453
|
A | T | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.493+1435A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778453 | ||||||
chr15:51778467
|
C | A | 1 | a0001c0001t0002g0130 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.493+1449C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778467 | ||||||
chr15:51778507
|
T | TA | 126 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(123): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.493+1502dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778507 | |||||
chr15:51778508
|
A | T | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.493+1490A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778508 | ||||||
chr15:51778517
|
A | AG | 8 | a0001c0001t0002g0130a0001c0001t0012g0017a0001c0001t0012g0132others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+1499_493+1500i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778517 | ||||||
chr15:51778638
|
T | G | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+1620T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778638 | ||||||
chr15:51778643
|
C | CT | 129 | a0001c0001t0001g0283a0001c0001t0001g0293a0001c0001t0001g0296others(126): Show | 135 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.493+1651dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | |||||
chr15:51778643
|
C | CTT | 33 | a0001c0001t0002g0022a0001c0001t0002g0052a0001c0001t0002g0056others(30): Show | 33 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.493+1650_493+1651d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | |||||
chr15:51778643
|
CT | C | 33 | a0001c0001t0003g0003a0001c0001t0003g0211a0001c0001t0003g0212others(30): Show | 39 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.493+1651delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | |||||
chr15:51778643
|
CTT | C | 15 | a0001c0001t0001g0285a0001c0001t0001g0302a0001c0001t0001g0344others(12): Show | 16 | HG00140.hp2 HG00733.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+1650_493+1651d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | |||||
chr15:51778643
|
CTTT | C | 29 | a0001c0001t0002g0087a0001c0001t0005g0011a0001c0001t0005g0177others(26): Show | 31 | HG00544.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.493+1649_493+1651d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51778643 | |||||
chr15:51778667
|
T | C | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.493+1649T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778667 | ||||||
chr15:51778747
|
T | G | 9 | a0001c0001t0001g0279a0001c0001t0001g0284a0001c0001t0001g0293others(6): Show | 9 | HG02155.hp2 NA18612.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.493+1729T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778747 | ||||||
chr15:51778810
|
A | G | 17 | a0001c0001t0003g0003a0001c0001t0003g0210a0001c0001t0003g0213others(14): Show | 20 | HG00639.hp2 HG00733.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.493+1792A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778810 | ||||||
chr15:51778830
|
A | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG02615.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.493+1812A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778830 | ||||||
chr15:51778980
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.493+1962A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51778980 | ||||||
chr15:51779089
|
G | A | 3 | a0001c0001t0017g0004a0001c0001t0017g0149a0001c0001t0024g0009 | 5 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-1955G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779089 | ||||||
chr15:51779241
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.494-1803C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779241 | ||||||
chr15:51779242
|
G | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-1802G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779242 | ||||||
chr15:51779273
|
T | A | 1 | a0001c0001t0001g0351 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.494-1771T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779273 | ||||||
chr15:51779411
|
C | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-1633C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779411 | ||||||
chr15:51779442
|
A | G | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.494-1602A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779442 | ||||||
chr15:51779460
|
A | G | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.494-1584A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779460 | ||||||
chr15:51779573
|
C | T | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.494-1471C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779573 | ||||||
chr15:51779686
|
C | CT | 33 | a0001c0001t0001g0351a0001c0001t0005g0011a0001c0001t0005g0177others(30): Show | 34 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.494-1346dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51779686 | |||||
chr15:51779686
|
CT | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-1346delT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 51779686 | |||||
chr15:51779743
|
C | A | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.494-1301C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779743 | ||||||
chr15:51779765
|
C | G | 1 | a0001c0001t0006g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.494-1279C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779765 | ||||||
chr15:51779940
|
C | A | 7 | a0001c0001t0009g0010a0001c0001t0009g0166a0001c0001t0009g0169others(4): Show | 8 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1104C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779940 | ||||||
chr15:51779941
|
C | A | 1 | a0001c0001t0029g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.494-1103C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51779941 | ||||||
chr15:51780016
|
T | C | 1 | a0001c0001t0011g0304 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.494-1028T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780016 | ||||||
chr15:51780023
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.494-1021G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780023 | ||||||
chr15:51780218
|
C | T | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.494-826C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780218 | ||||||
chr15:51780240
|
C | G | 1 | a0001c0001t0037g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.494-804C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780240 | ||||||
chr15:51780400
|
A | G | 130 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(127): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.494-644A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780400 | ||||||
chr15:51780437
|
T | C | 9 | a0001c0001t0002g0086a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG02074.hp1 HG02129.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-607T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780437 | ||||||
chr15:51780752
|
C | T | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-292C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 5/9 | chr15 | 51780752 | ||||||
chr15:51781210
|
A | ATCATGAG others(37): Show |
1 | a0001c0001t0001g0351 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.624+40_624+83dupTG others(42): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781210 | |||||
chr15:51781492
|
G | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.624+318G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781492 | ||||||
chr15:51781587
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+413G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781587 | ||||||
chr15:51781605
|
T | A | 38 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(35): Show | 39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+431T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781605 | ||||||
chr15:51781619
|
G | A | 146 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(143): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.624+445G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781619 | ||||||
chr15:51781651
|
T | C | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+477T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781651 | ||||||
chr15:51781695
|
G | A | 31 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.624+521G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781695 | ||||||
chr15:51781705
|
A | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(125): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.624+531A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781705 | ||||||
chr15:51781718
|
T | C | 128 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(125): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.624+544T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781718 | ||||||
chr15:51781803
|
G | GGA | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+649_624+650dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781803 | |||||
chr15:51781803
|
G | GGAGA | 74 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(71): Show | 80 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.624+647_624+650dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781803 | |||||
chr15:51781821
|
A | AGT | 141 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(138): Show | 148 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.624+648_624+649ins others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781821 | |||||
chr15:51781821
|
A | AGTGT | 6 | a0001c0001t0002g0019a0001c0001t0002g0083a0001c0001t0002g0084others(3): Show | 6 | HG01891.hp1 HG01928.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+648_624+649ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781821 | |||||
chr15:51781823
|
A | AGAGAGAG others(3): Show |
2 | a0001c0001t0001g0154a0001c0001t0018g0264 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.624+650_624+651ins others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | AGAGAGAG others(1): Show |
12 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(9): Show | 12 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | AGAGAGT | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | AGAGT | 5 | a0001c0001t0003g0249a0001c0001t0003g0250a0001c0001t0012g0133others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+650_624+651ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | AGT | 6 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0328others(3): Show | 6 | HG00639.hp1 HG00733.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+668_624+669dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | AGTGT | 6 | a0001c0001t0005g0177a0001c0001t0005g0182a0001c0001t0005g0183others(3): Show | 6 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+666_624+669dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51781823 | |||||
chr15:51781823
|
A | T | 149 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(146): Show | 156 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.624+649A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781823 | ||||||
chr15:51781824
|
G | T | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.624+650G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781824 | ||||||
chr15:51781825
|
T | A | 6 | a0001c0001t0003g0213a0001c0001t0003g0229a0001c0001t0003g0230others(3): Show | 6 | HG00323.hp2 HG01255.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+651T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781825 | ||||||
chr15:51781983
|
A | T | 1 | a0001c0001t0001g0318 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.625-738A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51781983 | ||||||
chr15:51782047
|
A | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-674A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782047 | ||||||
chr15:51782324
|
A | G | 1 | a0001c0001t0049g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625-397A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782324 | ||||||
chr15:51782376
|
G | A | 31 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.625-345G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782376 | ||||||
chr15:51782427
|
G | A | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-294G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782427 | ||||||
chr15:51782494
|
GACACTCA others(5): Show |
G | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.625-224_625-213del others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 51782494 | |||||
chr15:51782648
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.625-73G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 6/9 | chr15 | 51782648 | ||||||
chr15:51783060
|
T | C | 1 | a0001c0001t0008g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.732+232T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783060 | ||||||
chr15:51783271
|
C | T | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.732+443C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783271 | ||||||
chr15:51783398
|
C | T | 31 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+570C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783398 | ||||||
chr15:51783406
|
C | T | 1 | a0001c0001t0023g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.732+578C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783406 | ||||||
chr15:51783479
|
CA | C | 248 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(245): Show | 264 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.732+663delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783479 | |||||
chr15:51783520
|
A | T | 1 | a0001c0001t0001g0346 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.732+692A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783520 | ||||||
chr15:51783745
|
T | TGATA | 82 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0152others(79): Show | 86 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.732+962_732+965dup others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783745
|
T | TGATAGAT others(1): Show |
33 | a0001c0001t0001g0161a0001c0001t0001g0257a0001c0001t0001g0283others(30): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.732+958_732+965dup others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783745
|
T | TGATAGAT others(5): Show |
2 | a0001c0001t0001g0348a0001c0001t0014g0325 | 2 | NA18967.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.732+954_732+965dup others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783745
|
T | TGATAGAT others(13): Show |
1 | a0001c0001t0005g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.732+946_732+965dup others(20): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783745
|
TGATA | T | 22 | a0001c0001t0001g0281a0001c0001t0003g0212a0001c0001t0003g0230others(19): Show | 23 | HG00735.hp2 HG01081.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+962_732+965del others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783745
|
TGATAGAT others(1): Show |
T | 9 | a0001c0001t0001g0162a0001c0001t0007g0220a0001c0001t0007g0222others(6): Show | 9 | HG01255.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+958_732+965del others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783745 | |||||
chr15:51783775
|
A | ATAGATAG others(5): Show |
2 | a0001c0001t0006g0032a0001c0001t0006g0039 | 2 | NA19077.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.732+958_732+959ins others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | |||||
chr15:51783775
|
A | ATAGATAG others(1): Show |
10 | a0001c0001t0006g0005a0001c0001t0006g0034a0001c0001t0006g0035others(7): Show | 11 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+954_732+955ins others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | |||||
chr15:51783775
|
A | ATAGG | 20 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(17): Show | 20 | HG01433.hp1 HG01891.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.732+950_732+951ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783775 | |||||
chr15:51783775
|
A | G | 95 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(92): Show | 100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.732+947A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783775 | ||||||
chr15:51783791
|
A | ATAGG | 4 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(1): Show | 4 | NA18747.hp1 NA18971.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+965_732+966ins others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51783791 | |||||
chr15:51783791
|
A | G | 1 | a0001c0001t0013g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+963A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783791 | ||||||
chr15:51783887
|
T | C | 1 | a0001c0001t0018g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732+1059T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51783887 | ||||||
chr15:51784025
|
C | T | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+1197C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784025 | ||||||
chr15:51784047
|
T | C | 1 | a0001c0001t0008g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.732+1219T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784047 | ||||||
chr15:51784199
|
T | G | 131 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(128): Show | 139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.732+1371T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784199 | ||||||
chr15:51784325
|
C | CCA | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+1497_732+1498i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784325 | ||||||
chr15:51784326
|
G | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+1498G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784326 | ||||||
chr15:51784429
|
T | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+1601T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784429 | ||||||
chr15:51784540
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+1712A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784540 | ||||||
chr15:51784608
|
T | A | 38 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(35): Show | 39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.732+1780T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784608 | ||||||
chr15:51784659
|
A | G | 1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.732+1831A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784659 | ||||||
chr15:51784764
|
T | G | 22 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(19): Show | 23 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+1936T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784764 | ||||||
chr15:51784844
|
C | A | 188 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(185): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.732+2016C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784844 | ||||||
chr15:51784959
|
A | T | 1 | a0001c0001t0007g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+2131A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51784959 | ||||||
chr15:51785057
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.732+2229C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785057 | ||||||
chr15:51785135
|
G | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+2307G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785135 | ||||||
chr15:51785139
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0336 | 3 | HG01934.hp1 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.732+2311G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785139 | ||||||
chr15:51785184
|
G | A | 1 | a0001c0001t0008g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.732+2356G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785184 | ||||||
chr15:51785275
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+2447G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785275 | ||||||
chr15:51785411
|
C | CA | 25 | a0001c0001t0005g0011a0001c0001t0005g0179a0001c0001t0005g0180others(22): Show | 26 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.732+2605dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | |||||
chr15:51785411
|
CA | C | 274 | a0001c0001t0001g0016a0001c0001t0001g0254a0001c0001t0001g0255others(271): Show | 287 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.732+2605delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | |||||
chr15:51785411
|
CAA | C | 16 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0006g0031others(13): Show | 18 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.732+2604_732+2605d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | |||||
chr15:51785411
|
CAAA | C | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+2603_732+2605d others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51785411 | |||||
chr15:51785532
|
G | A | 38 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(35): Show | 39 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.732+2704G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785532 | ||||||
chr15:51785962
|
A | T | 1 | a0001c0001t0001g0345 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.732+3134A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51785962 | ||||||
chr15:51786038
|
G | A | 169 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(166): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.732+3210G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786038 | ||||||
chr15:51786154
|
A | G | 15 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(12): Show | 16 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+3326A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786154 | ||||||
chr15:51786206
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+3378C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786206 | ||||||
chr15:51786282
|
G | A | 32 | a0001c0001t0002g0095a0001c0001t0005g0011a0001c0001t0005g0177others(29): Show | 33 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.732+3454G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786282 | ||||||
chr15:51786366
|
C | T | 130 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(127): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.732+3538C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786366 | ||||||
chr15:51786615
|
G | A | 52 | a0001c0001t0003g0003a0001c0001t0003g0210a0001c0001t0003g0211others(49): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.732+3787G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786615 | ||||||
chr15:51786716
|
A | G | 1 | a0001c0001t0010g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.732+3888A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786716 | ||||||
chr15:51786964
|
A | T | 28 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(25): Show | 29 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.732+4136A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51786964 | ||||||
chr15:51787129
|
CCG | C | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.732+4305_732+4306d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51787129 | |||||
chr15:51787275
|
G | C | 1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.732+4447G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787275 | ||||||
chr15:51787311
|
G | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+4483G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787311 | ||||||
chr15:51787354
|
G | C | 1 | a0001c0001t0035g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.732+4526G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787354 | ||||||
chr15:51787402
|
G | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+4574G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787402 | ||||||
chr15:51787662
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.732+4834T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787662 | ||||||
chr15:51787672
|
A | G | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+4844A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787672 | ||||||
chr15:51787752
|
C | T | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+4924C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51787752 | ||||||
chr15:51788024
|
A | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.732+5196A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788024 | ||||||
chr15:51788182
|
A | C | 128 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(125): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.732+5354A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788182 | ||||||
chr15:51788344
|
A | G | 15 | a0001c0001t0007g0013a0001c0001t0007g0206a0001c0001t0007g0207others(12): Show | 16 | HG01255.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+5516A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788344 | ||||||
chr15:51788368
|
G | C | 183 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(180): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.732+5540G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788368 | ||||||
chr15:51788467
|
G | A | 1 | a0001c0001t0004g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.732+5639G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788467 | ||||||
chr15:51788473
|
C | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+5645C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788473 | ||||||
chr15:51788518
|
G | A | 2 | a0001c0001t0016g0141a0001c0001t0016g0142 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+5690G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788518 | ||||||
chr15:51788606
|
T | C | 145 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(142): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.732+5778T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788606 | ||||||
chr15:51788611
|
G | C | 3 | a0001c0001t0008g0261a0001c0001t0008g0267a0001c0001t0008g0274 | 3 | NA18969.hp2 NA19002.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.732+5783G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788611 | ||||||
chr15:51788829
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6001A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788829 | ||||||
chr15:51788836
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6008T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788836 | ||||||
chr15:51788839
|
C | A | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6011C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788839 | ||||||
chr15:51788871
|
T | A | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6043T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788871 | ||||||
chr15:51788880
|
C | T | 1 | a0001c0001t0038g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.732+6052C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788880 | ||||||
chr15:51788922
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6094G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788922 | ||||||
chr15:51788927
|
C | G | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6099C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788927 | ||||||
chr15:51788932
|
T | G | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6104T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788932 | ||||||
chr15:51788942
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6114A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788942 | ||||||
chr15:51788949
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6121T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788949 | ||||||
chr15:51788953
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6125T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788953 | ||||||
chr15:51788970
|
G | A | 1 | a0001c0001t0008g0267 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.732+6142G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788970 | ||||||
chr15:51788974
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.732+6146G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51788974 | ||||||
chr15:51789037
|
A | G | 15 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0027others(12): Show | 16 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+6209A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789037 | ||||||
chr15:51789141
|
C | T | 17 | a0001c0001t0008g0203a0001c0001t0008g0260a0001c0001t0008g0261others(14): Show | 17 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+6313C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789141 | ||||||
chr15:51789242
|
A | G | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.732+6414A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789242 | ||||||
chr15:51789314
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.732+6486G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789314 | ||||||
chr15:51789401
|
G | A | 2 | a0001c0001t0005g0187a0001c0001t0005g0189 | 2 | NA18747.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.732+6573G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789401 | ||||||
chr15:51789428
|
A | G | 1 | a0001c0001t0054g0199 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.732+6600A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789428 | ||||||
chr15:51789445
|
G | A | 17 | a0001c0001t0008g0203a0001c0001t0008g0260a0001c0001t0008g0261others(14): Show | 17 | HG01358.hp2 HG02056.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+6617G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789445 | ||||||
chr15:51789577
|
G | A | 1 | a0001c0001t0026g0252 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.732+6749G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789577 | ||||||
chr15:51789584
|
C | T | 169 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(166): Show | 178 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.732+6756C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789584 | ||||||
chr15:51789600
|
A | G | 31 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+6772A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789600 | ||||||
chr15:51789601
|
T | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+6773T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789601 | ||||||
chr15:51789640
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732+6812C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789640 | ||||||
chr15:51789816
|
A | G | 128 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(125): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.732+6988A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789816 | ||||||
chr15:51789862
|
G | T | 1 | a0001c0001t0018g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+7034G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789862 | ||||||
chr15:51789885
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.732+7057T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789885 | ||||||
chr15:51789923
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.732+7095G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51789923 | ||||||
chr15:51790012
|
A | G | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.732+7184A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790012 | ||||||
chr15:51790049
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.732+7221C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790049 | ||||||
chr15:51790074
|
G | A | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+7246G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790074 | ||||||
chr15:51790151
|
C | G | 1 | a0001c0001t0001g0354 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.732+7323C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790151 | ||||||
chr15:51790233
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7405C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790233 | ||||||
chr15:51790357
|
A | G | 1 | a0001c0001t0028g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.732+7529A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790357 | ||||||
chr15:51790408
|
G | T | 1 | a0001c0001t0009g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.732+7580G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790408 | ||||||
chr15:51790449
|
C | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7621C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790449 | ||||||
chr15:51790468
|
G | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+7640G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790468 | ||||||
chr15:51790561
|
G | A | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-7636G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790561 | ||||||
chr15:51790633
|
G | A | 2 | a0001c0001t0003g0229a0001c0001t0003g0231 | 2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.733-7564G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790633 | ||||||
chr15:51790656
|
A | G | 1 | a0001c0001t0007g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.733-7541A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790656 | ||||||
chr15:51790823
|
C | T | 9 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(6): Show | 10 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-7374C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790823 | ||||||
chr15:51790849
|
G | A | 2 | a0001c0001t0020g0057a0001c0001t0020g0113 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.733-7348G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790849 | ||||||
chr15:51790982
|
A | G | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.733-7215A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51790982 | ||||||
chr15:51791160
|
C | T | 52 | a0001c0001t0003g0003a0001c0001t0003g0210a0001c0001t0003g0211others(49): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.733-7037C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791160 | ||||||
chr15:51791504
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6693A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791504 | ||||||
chr15:51791665
|
C | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6532C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791665 | ||||||
chr15:51791715
|
A | G | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-6482A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791715 | ||||||
chr15:51791728
|
C | A | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6469C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791728 | ||||||
chr15:51791729
|
A | C | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6468A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791729 | ||||||
chr15:51791732
|
C | A | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-6465C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791732 | ||||||
chr15:51791764
|
C | G | 1 | a0001c0001t0002g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.733-6433C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51791764 | ||||||
chr15:51792033
|
G | T | 130 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(127): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.733-6164G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792033 | ||||||
chr15:51792110
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-6087C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792110 | ||||||
chr15:51792220
|
C | A | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-5977C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792220 | ||||||
chr15:51792253
|
T | C | 1 | a0001c0001t0007g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733-5944T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792253 | ||||||
chr15:51792265
|
C | T | 23 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(20): Show | 24 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.733-5932C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792265 | ||||||
chr15:51792317
|
C | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-5880C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792317 | ||||||
chr15:51792328
|
G | A | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-5869G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792328 | ||||||
chr15:51792409
|
T | C | 130 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(127): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.733-5788T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792409 | ||||||
chr15:51792721
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733-5476G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792721 | ||||||
chr15:51792780
|
C | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-5417C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792780 | ||||||
chr15:51792885
|
G | A | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.733-5312G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792885 | ||||||
chr15:51792951
|
G | T | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-5246G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51792951 | ||||||
chr15:51793178
|
A | T | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-5019A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793178 | ||||||
chr15:51793329
|
A | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG02615.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.733-4868A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793329 | ||||||
chr15:51793364
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.733-4833A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793364 | ||||||
chr15:51793439
|
G | A | 2 | a0001c0001t0003g0249a0001c0001t0003g0250 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.733-4758G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793439 | ||||||
chr15:51793503
|
T | A | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.733-4694T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793503 | ||||||
chr15:51793618
|
C | T | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-4579C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793618 | ||||||
chr15:51793777
|
G | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4420G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793777 | ||||||
chr15:51793807
|
G | A | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-4390G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793807 | ||||||
chr15:51793818
|
T | G | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-4379T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793818 | ||||||
chr15:51793879
|
T | A | 7 | a0001c0001t0005g0177a0001c0001t0005g0182a0001c0001t0005g0183others(4): Show | 7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4318T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793879 | ||||||
chr15:51793880
|
G | T | 7 | a0001c0001t0005g0177a0001c0001t0005g0182a0001c0001t0005g0183others(4): Show | 7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4317G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793880 | ||||||
chr15:51793881
|
C | T | 7 | a0001c0001t0005g0177a0001c0001t0005g0182a0001c0001t0005g0183others(4): Show | 7 | NA18612.hp1 NA18959.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-4316C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793881 | ||||||
chr15:51793974
|
G | A | 1 | a0001c0001t0008g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.733-4223G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51793974 | ||||||
chr15:51794092
|
G | C | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-4105G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794092 | ||||||
chr15:51794105
|
C | T | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-4092C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794105 | ||||||
chr15:51794214
|
C | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-3983C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794214 | ||||||
chr15:51794225
|
G | A | 3 | a0001c0001t0008g0261a0001c0001t0008g0267a0001c0001t0008g0274 | 3 | NA18969.hp2 NA19002.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.733-3972G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794225 | ||||||
chr15:51794532
|
T | C | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.733-3665T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794532 | ||||||
chr15:51794569
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.733-3628G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794569 | ||||||
chr15:51794630
|
T | A | 1 | a0001c0001t0013g0148 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733-3567T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794630 | ||||||
chr15:51794660
|
C | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-3537C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794660 | ||||||
chr15:51794780
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.733-3417A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794780 | ||||||
chr15:51794793
|
A | T | 24 | a0001c0001t0004g0045a0001c0001t0004g0049a0001c0001t0004g0050others(21): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.733-3404A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794793 | ||||||
chr15:51794806
|
A | G | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-3391A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51794806 | ||||||
chr15:51795024
|
C | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.733-3173C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795024 | ||||||
chr15:51795080
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.733-3117C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795080 | ||||||
chr15:51795227
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2970C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795227 | ||||||
chr15:51795229
|
T | C | 1 | a0002c0002t0004g0061 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.733-2968T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795229 | ||||||
chr15:51795250
|
G | A | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-2947G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795250 | ||||||
chr15:51795268
|
TA | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-2921delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795268 | |||||
chr15:51795428
|
C | CA | 115 | a0001c0001t0001g0016a0001c0001t0001g0258a0001c0001t0001g0259others(112): Show | 116 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.733-2753dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795428 | |||||
chr15:51795428
|
CA | C | 53 | a0001c0001t0004g0069a0001c0001t0005g0011a0001c0001t0005g0177others(50): Show | 55 | HG00423.hp2 HG00544.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.733-2753delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795428 | |||||
chr15:51795442
|
A | AG | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-2755_733-2754i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795442 | ||||||
chr15:51795466
|
G | C | 1 | a0001c0001t0017g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-2731G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795466 | ||||||
chr15:51795475
|
G | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2722G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795475 | ||||||
chr15:51795563
|
CTGCT | C | 20 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0257others(17): Show | 21 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.733-2620_733-2617d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | |||||
chr15:51795563
|
CTGCTTGC others(1): Show |
C | 20 | a0001c0001t0001g0295a0001c0001t0002g0021a0001c0001t0002g0115others(17): Show | 22 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.733-2624_733-2617d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | |||||
chr15:51795563
|
CTGCTTGC others(5): Show |
C | 26 | a0001c0001t0002g0020a0001c0001t0005g0011a0001c0001t0005g0177others(23): Show | 29 | HG00423.hp2 HG00544.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.733-2628_733-2617d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795563 | |||||
chr15:51795565
|
GCTTGCTT others(9): Show |
G | 26 | a0001c0001t0002g0019a0001c0001t0005g0179a0001c0001t0005g0180others(23): Show | 26 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-2628_733-2613d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(13): Show |
G | 14 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(11): Show | 14 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.733-2628_733-2609d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(17): Show |
G | 19 | a0001c0001t0002g0051a0001c0001t0002g0097a0001c0001t0002g0103others(16): Show | 19 | HG00140.hp1 HG00741.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.733-2628_733-2605d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(21): Show |
G | 40 | a0001c0001t0002g0044a0001c0001t0002g0055a0001c0001t0002g0056others(37): Show | 42 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-2628_733-2601d others(30): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(25): Show |
G | 19 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0052others(16): Show | 20 | HG00408.hp2 HG00741.hp2 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.733-2628_733-2597d others(34): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(29): Show |
G | 9 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0087others(6): Show | 11 | HG02451.hp2 HG02523.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-2628_733-2593d others(38): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795565
|
GCTTGCTT others(33): Show |
G | 5 | a0001c0001t0002g0094a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG00323.hp1 HG00609.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2628_733-2589d others(42): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795565 | |||||
chr15:51795569
|
G | T | 2 | a0001c0001t0006g0039a0001c0001t0010g0122 | 2 | HG02280.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.733-2628G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795569 | ||||||
chr15:51795569
|
GCTTGCTT others(5): Show |
G | 8 | a0001c0001t0003g0213a0001c0001t0003g0219a0001c0001t0003g0231others(5): Show | 8 | HG01081.hp2 HG01433.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-2624_733-2613d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | |||||
chr15:51795569
|
GCTTGCTT others(9): Show |
G | 3 | a0001c0001t0007g0206a0001c0001t0013g0145a0001c0001t0013g0146 | 3 | HG03540.hp2 NA18747.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.733-2624_733-2609d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | |||||
chr15:51795569
|
GCTTGCTT others(13): Show |
G | 3 | a0001c0001t0010g0048a0001c0001t0013g0147a0001c0001t0013g0148 | 3 | HG02145.hp1 HG04115.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.733-2624_733-2605d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | |||||
chr15:51795569
|
GCTTGCTT others(17): Show |
G | 4 | a0001c0001t0007g0207a0001c0001t0007g0221a0001c0001t0007g0222others(1): Show | 4 | HG02257.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-2624_733-2601d others(26): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | |||||
chr15:51795569
|
GCTTGCTT others(21): Show |
G | 6 | a0001c0001t0007g0013a0001c0001t0007g0220a0001c0001t0007g0223others(3): Show | 7 | HG01255.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-2624_733-2597d others(30): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795569 | |||||
chr15:51795573
|
G | T | 14 | a0001c0001t0002g0022a0001c0001t0003g0228a0001c0001t0003g0245others(11): Show | 14 | HG00738.hp1 HG01081.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.733-2624G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795573 | ||||||
chr15:51795573
|
GCTTGCTT others(1): Show |
G | 5 | a0001c0001t0001g0256a0001c0001t0003g0211a0001c0001t0003g0244others(2): Show | 6 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-2620_733-2613d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | |||||
chr15:51795573
|
GCTTGCTT others(5): Show |
G | 5 | a0001c0001t0003g0003a0001c0001t0007g0012a0001c0001t0007g0214others(2): Show | 8 | HG01074.hp2 HG01516.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-2620_733-2609d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | |||||
chr15:51795573
|
GCTTGCTT others(9): Show |
G | 3 | a0001c0001t0007g0215a0001c0001t0007g0238a0001c0001t0014g0316 | 3 | HG02970.hp1 NA18522.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.733-2620_733-2605d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | |||||
chr15:51795573
|
GCTTGCTT others(13): Show |
G | 3 | a0001c0001t0019g0204a0001c0001t0019g0205a0001c0001t0019g0208 | 3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.733-2620_733-2601d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795573 | |||||
chr15:51795577
|
G | GCTTT | 5 | a0001c0001t0001g0291a0001c0001t0001g0302a0001c0001t0001g0323others(2): Show | 5 | NA18612.hp2 NA18980.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2561_733-2558d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
G | GCTTTCTT others(1): Show |
3 | a0001c0001t0001g0284a0001c0001t0001g0315a0001c0001t0001g0350 | 3 | HG02155.hp2 NA18952.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.733-2565_733-2558d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
G | GCTTTCTT others(5): Show |
1 | a0001c0001t0001g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.733-2569_733-2558d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
G | T | 52 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(49): Show | 54 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.733-2620G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795577 | ||||||
chr15:51795577
|
GCTTT | G | 18 | a0001c0001t0001g0258a0001c0001t0001g0308a0001c0001t0001g0311others(15): Show | 18 | HG00609.hp1 HG01109.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.733-2561_733-2558d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
GCTTTCTT others(1): Show |
G | 14 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0001g0303others(11): Show | 14 | HG00642.hp1 HG01358.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.733-2565_733-2558d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
GCTTTCTT others(5): Show |
G | 4 | a0001c0001t0001g0319a0001c0001t0001g0336a0001c0001t0001g0345others(1): Show | 4 | HG00639.hp1 HG00733.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2569_733-2558d others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
GCTTTCTT others(9): Show |
G | 1 | a0001c0001t0025g0352 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.733-2573_733-2558d others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795577
|
GCTTTCTT others(13): Show |
G | 4 | a0001c0001t0001g0016a0001c0001t0001g0300a0001c0001t0001g0337others(1): Show | 5 | HG00544.hp2 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2577_733-2558d others(22): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795577 | |||||
chr15:51795581
|
T | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0327a0001c0001t0001g0351others(1): Show | 4 | NA18957.hp2 NA18979.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2616T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795581 | ||||||
chr15:51795585
|
T | G | 4 | a0001c0001t0001g0332a0001c0001t0018g0264a0001c0001t0018g0265others(1): Show | 4 | HG00609.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2612T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795585 | ||||||
chr15:51795589
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.733-2608T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795589 | ||||||
chr15:51795593
|
T | G | 2 | a0001c0001t0001g0319a0001c0001t0001g0345 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.733-2604T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795593 | ||||||
chr15:51795597
|
T | G | 1 | a0001c0001t0025g0352 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.733-2600T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795597 | ||||||
chr15:51795610
|
C | CTTTCT | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02258.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.733-2584_733-2580d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | |||||
chr15:51795610
|
C | CTTTCTTT others(2): Show |
7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-2584_733-2576d others(11): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | |||||
chr15:51795610
|
C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.733-2584_733-2572d others(15): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795610 | |||||
chr15:51795636
|
T | C | 1 | a0001c0001t0005g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.733-2561T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795636 | ||||||
chr15:51795678
|
C | T | 1 | a0001c0001t0018g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.733-2519C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795678 | ||||||
chr15:51795679
|
A | G | 4 | a0001c0001t0002g0115a0001c0001t0020g0057a0001c0001t0020g0113others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-2518A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795679 | ||||||
chr15:51795709
|
C | T | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.733-2488C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795709 | ||||||
chr15:51795713
|
A | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-2484A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795713 | ||||||
chr15:51795909
|
A | G | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-2288A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51795909 | ||||||
chr15:51795929
|
CTTTCTT | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2255_733-2250d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51795929 | |||||
chr15:51796094
|
T | TATTTTTG | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-2102_733-2101i others(9): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51796094 | |||||
chr15:51796533
|
T | C | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-1664T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796533 | ||||||
chr15:51796569
|
C | G | 2 | a0001c0001t0028g0078a0001c0001t0031g0079 | 2 | HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.733-1628C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796569 | ||||||
chr15:51796699
|
A | C | 1 | a0001c0001t0003g0232 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.733-1498A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796699 | ||||||
chr15:51796959
|
T | C | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.733-1238T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796959 | ||||||
chr15:51796971
|
G | C | 1 | a0001c0001t0003g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.733-1226G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796971 | ||||||
chr15:51796991
|
C | G | 37 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(34): Show | 38 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.733-1206C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51796991 | ||||||
chr15:51797088
|
G | A | 1 | a0001c0001t0017g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-1109G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797088 | ||||||
chr15:51797114
|
A | C | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-1083A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797114 | ||||||
chr15:51797234
|
T | C | 168 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(165): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.733-963T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797234 | ||||||
chr15:51797261
|
C | A | 1 | a0001c0001t0049g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.733-936C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797261 | ||||||
chr15:51797424
|
C | T | 15 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0027others(12): Show | 16 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-773C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797424 | ||||||
chr15:51797500
|
A | G | 1 | a0001c0001t0028g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.733-697A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797500 | ||||||
chr15:51797503
|
C | T | 37 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(34): Show | 38 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.733-694C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797503 | ||||||
chr15:51797574
|
A | G | 1 | a0001c0001t0001g0348 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.733-623A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797574 | ||||||
chr15:51797605
|
G | A | 30 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(27): Show | 31 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.733-592G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797605 | ||||||
chr15:51797628
|
C | A | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.733-569C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797628 | ||||||
chr15:51797629
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.733-568C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797629 | ||||||
chr15:51797630
|
G | C | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.733-567G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797630 | ||||||
chr15:51797745
|
A | G | 1 | a0001c0001t0042g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.733-452A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797745 | ||||||
chr15:51797795
|
T | A | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-402T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797795 | ||||||
chr15:51797881
|
C | CA | 24 | a0001c0001t0001g0292a0001c0001t0001g0309a0001c0001t0002g0056others(21): Show | 26 | HG00140.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-303dupA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | |||||
chr15:51797881
|
CA | C | 31 | a0001c0001t0004g0067a0001c0001t0004g0069a0001c0001t0005g0011others(28): Show | 32 | HG00544.hp1 HG01106.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.733-303delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | |||||
chr15:51797881
|
CAA | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-304_733-303del others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797881 | |||||
chr15:51797903
|
G | GTT | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-286_733-285dup others(2): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 51797903 | |||||
chr15:51797993
|
T | G | 1 | a0001c0001t0002g0110 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.733-204T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 7/9 | chr15 | 51797993 | ||||||
chr15:51798508
|
A | G | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+168A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798508 | ||||||
chr15:51798527
|
A | G | 1 | a0001c0001t0007g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.876+187A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798527 | ||||||
chr15:51798684
|
T | G | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.876+344T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798684 | ||||||
chr15:51798970
|
G | A | 184 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.876+630G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51798970 | ||||||
chr15:51799022
|
C | T | 1 | a0001c0001t0024g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.876+682C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799022 | ||||||
chr15:51799330
|
G | T | 185 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(182): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.876+990G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799330 | ||||||
chr15:51799435
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.876+1095C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799435 | ||||||
chr15:51799505
|
G | C | 3 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG02155.hp2 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.876+1165G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799505 | ||||||
chr15:51799521
|
AG | A | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(120): Show | 130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.876+1182delG | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799521 | ||||||
chr15:51799588
|
G | A | 175 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(172): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.876+1248G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799588 | ||||||
chr15:51799609
|
G | A | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+1269G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51799609 | ||||||
chr15:51799630
|
A | ATG | 4 | a0001c0001t0002g0115a0001c0001t0020g0057a0001c0001t0020g0113others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+1293_876+1294d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51799630 | |||||
chr15:51800124
|
C | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+1784C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800124 | ||||||
chr15:51800246
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.876+1906T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800246 | ||||||
chr15:51800396
|
T | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.876+2056T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800396 | ||||||
chr15:51800488
|
A | G | 1 | a0001c0001t0010g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.876+2148A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800488 | ||||||
chr15:51800529
|
G | A | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2189G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800529 | ||||||
chr15:51800583
|
C | A | 3 | a0001c0001t0010g0048a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02145.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.876+2243C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800583 | ||||||
chr15:51800627
|
T | G | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2287T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800627 | ||||||
chr15:51800755
|
GAGTACAA others(6): Show |
G | 1 | a0001c0001t0002g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.876+2419_876+2431d others(15): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51800755 | |||||
chr15:51800907
|
A | G | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+2567A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51800907 | ||||||
chr15:51801217
|
C | CCT | 39 | a0001c0001t0001g0298a0001c0001t0001g0326a0001c0001t0002g0001others(36): Show | 40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.876+2897_876+2898d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | |||||
chr15:51801217
|
C | CCTCT | 3 | a0001c0001t0002g0174a0001c0001t0021g0047a0001c0001t0021g0090 | 3 | HG00609.hp2 HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.876+2895_876+2898d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | |||||
chr15:51801217
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.876+2877C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801217 | ||||||
chr15:51801217
|
CCT | C | 21 | a0001c0001t0001g0159a0001c0001t0001g0291a0001c0001t0001g0297others(18): Show | 25 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.876+2897_876+2898d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | |||||
chr15:51801217
|
CCTCTCT | C | 3 | a0001c0001t0001g0154a0001c0001t0012g0017a0001c0001t0012g0137 | 3 | HG01884.hp2 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.876+2893_876+2898d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801217 | |||||
chr15:51801225
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.876+2885T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801225 | ||||||
chr15:51801229
|
T | TCA | 6 | a0001c0001t0001g0152a0001c0001t0009g0010a0001c0001t0009g0164others(3): Show | 7 | HG00140.hp2 HG02965.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.876+2890_876+2891i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801229 | |||||
chr15:51801229
|
T | TCACA | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0009g0169others(2): Show | 5 | HG02280.hp2 HG03130.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2890_876+2891i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801229 | |||||
chr15:51801231
|
T | A | 17 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(14): Show | 18 | HG00140.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.876+2891T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801231 | ||||||
chr15:51801231
|
TCTCTCTC others(1): Show |
T | 5 | a0001c0001t0012g0132a0001c0001t0012g0133a0001c0001t0012g0134others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2893_876+2900d others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801231 | |||||
chr15:51801233
|
T | A | 20 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 21 | HG00140.hp2 HG02280.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.876+2893T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801233 | ||||||
chr15:51801233
|
T | TCACACAC others(3): Show |
2 | a0001c0001t0010g0119a0001c0001t0010g0120 | 2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | |||||
chr15:51801233
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0010g0048a0001c0001t0010g0122 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | |||||
chr15:51801233
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0010g0008 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.876+2894_876+2895i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801233 | |||||
chr15:51801235
|
T | A | 31 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(28): Show | 33 | HG00140.hp2 HG01243.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.876+2895T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801235 | ||||||
chr15:51801235
|
T | TCA | 9 | a0001c0001t0001g0322a0001c0001t0003g0212a0001c0001t0003g0229others(6): Show | 10 | HG00323.hp2 HG00642.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACA | 4 | a0001c0001t0003g0231a0001c0001t0003g0235a0001c0001t0003g0249others(1): Show | 4 | HG00735.hp2 HG00738.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACACA | 5 | a0001c0001t0003g0233a0001c0001t0007g0215a0001c0001t0007g0220others(2): Show | 5 | HG02647.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACACAC others(1): Show |
6 | a0001c0001t0003g0230a0001c0001t0007g0206a0001c0001t0007g0207others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+2896_876+2897i others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACACAC others(3): Show |
2 | a0001c0001t0007g0012a0001c0001t0007g0214 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.876+2896_876+2897i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0007g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.876+2896_876+2897i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0007g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.876+2896_876+2897i others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
TCTCA | T | 6 | a0001c0001t0007g0238a0001c0001t0013g0143a0001c0001t0013g0145others(3): Show | 6 | HG02970.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+2897_876+2900d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801235
|
TCTCACA | T | 3 | a0001c0001t0003g0213a0001c0001t0003g0245a0001c0001t0013g0147 | 3 | HG03834.hp2 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.876+2897_876+2902d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801235 | |||||
chr15:51801237
|
T | A | 72 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(69): Show | 76 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.876+2897T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801237 | ||||||
chr15:51801237
|
T | TCA | 24 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0308others(21): Show | 24 | HG00408.hp1 HG01109.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.876+2943_876+2944d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCACA | 3 | a0001c0001t0001g0272a0001c0001t0001g0279a0001c0001t0001g0299 | 3 | HG02572.hp1 NA18957.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.876+2941_876+2944d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCACACA | 2 | a0001c0001t0005g0185a0001c0001t0017g0004 | 3 | HG01167.hp1 HG01169.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.876+2939_876+2944d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCACACAC others(3): Show |
7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0125others(4): Show | 7 | HG01123.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2935_876+2944d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCA | 16 | a0001c0001t0002g0007a0001c0001t0002g0056a0001c0001t0002g0096others(13): Show | 17 | HG00408.hp2 HG00738.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACA | 8 | a0001c0001t0002g0044a0001c0001t0002g0083a0001c0001t0002g0093others(5): Show | 8 | HG01496.hp2 HG02257.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACAC others(1): Show |
4 | a0001c0001t0002g0051a0001c0001t0002g0102a0001c0001t0002g0112others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(10): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACAC others(3): Show |
12 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0187others(9): Show | 12 | HG01106.hp2 HG01943.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACAC others(5): Show |
5 | a0001c0001t0002g0081a0001c0001t0002g0101a0001c0001t0005g0011others(2): Show | 6 | HG00544.hp1 HG01433.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+2898_876+2899i others(14): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACAC others(7): Show |
1 | a0001c0001t0005g0193 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.876+2898_876+2899i others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCACAC others(9): Show |
1 | a0001c0001t0005g0186 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.876+2898_876+2899i others(18): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
T | TCTCTCAC others(3): Show |
1 | a0001c0001t0002g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.876+2898_876+2899i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
TCA | T | 31 | a0001c0001t0001g0273a0001c0001t0001g0296a0001c0001t0001g0339others(28): Show | 33 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.876+2943_876+2944d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
TCACA | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0300a0001c0001t0001g0310others(8): Show | 12 | HG00544.hp2 HG01934.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+2941_876+2944d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801237
|
TCACACAC others(7): Show |
T | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG01109.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+2931_876+2944d others(16): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801237 | |||||
chr15:51801239
|
A | T | 23 | a0001c0001t0001g0324a0001c0001t0002g0002a0001c0001t0002g0053others(20): Show | 24 | HG00140.hp1 HG00741.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.876+2899A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801239 | ||||||
chr15:51801241
|
A | T | 22 | a0001c0001t0002g0002a0001c0001t0002g0080a0001c0001t0002g0094others(19): Show | 25 | HG00323.hp1 HG00423.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.876+2901A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801241 | ||||||
chr15:51801275
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+2944_876+2945i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801275 | |||||
chr15:51801281
|
A | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2941A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801281 | ||||||
chr15:51801283
|
A | C | 3 | a0001c0001t0006g0040a0001c0001t0006g0042a0001c0001t0040g0030 | 3 | NA18943.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.876+2943A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | ||||||
chr15:51801283
|
A | G | 1 | a0001c0001t0048g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.876+2943A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | ||||||
chr15:51801283
|
A | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2943A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801283 | ||||||
chr15:51801284
|
C | CACA | 3 | a0001c0001t0002g0139a0001c0001t0015g0239a0001c0001t0035g0018 | 3 | HG00741.hp2 HG01081.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.876+2944_876+2945i others(5): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | ||||||
chr15:51801284
|
C | CTG | 3 | a0001c0001t0006g0040a0001c0001t0006g0042a0001c0001t0040g0030 | 3 | NA18943.hp2 NA18965.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.876+2944_876+2945i others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | ||||||
chr15:51801284
|
C | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+2944C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801284 | ||||||
chr15:51801285
|
C | T | 10 | a0001c0001t0006g0040a0001c0001t0006g0042a0001c0001t0012g0017others(7): Show | 10 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.876+2945C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801285 | ||||||
chr15:51801288
|
G | C | 11 | a0001c0001t0006g0035a0001c0001t0006g0040a0001c0001t0006g0042others(8): Show | 11 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+2948G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801288 | ||||||
chr15:51801288
|
G | GTC | 8 | a0001c0001t0001g0151a0001c0001t0002g0019a0001c0001t0002g0020others(5): Show | 8 | HG01891.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.876+2974_876+2975d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | |||||
chr15:51801288
|
G | GTCTC | 20 | a0001c0001t0006g0005a0001c0001t0006g0024a0001c0001t0006g0025others(17): Show | 21 | HG00423.hp2 HG01257.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.876+2972_876+2975d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | |||||
chr15:51801288
|
G | GTCTCTC | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.876+2970_876+2975d others(8): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | |||||
chr15:51801288
|
GTC | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(94): Show | 101 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.876+2974_876+2975d others(4): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | |||||
chr15:51801288
|
GTCTC | G | 13 | a0001c0001t0002g0123a0001c0001t0009g0010a0001c0001t0009g0165others(10): Show | 14 | HG02145.hp2 HG03209.hp2 HG03579.hp2 others(11): Show |
intron_variant | MODIFIER | c.876+2972_876+2975d others(6): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801288 | |||||
chr15:51801316
|
A | G | 1 | a0001c0001t0009g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.876+2976A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801316 | ||||||
chr15:51801380
|
G | A | 1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+3040G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801380 | ||||||
chr15:51801591
|
G | T | 1 | a0001c0001t0049g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.876+3251G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801591 | ||||||
chr15:51801655
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.876+3315G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801655 | ||||||
chr15:51801734
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+3394A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801734 | ||||||
chr15:51801889
|
C | T | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(121): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.876+3549C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801889 | ||||||
chr15:51801914
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+3574A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801914 | ||||||
chr15:51801918
|
C | T | 2 | a0001c0001t0004g0068a0001c0001t0004g0072 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.876+3578C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51801918 | ||||||
chr15:51801947
|
T | TATAAC | 176 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(173): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.876+3612_876+3616d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801947 | |||||
chr15:51801947
|
T | TATAACAT others(3): Show |
1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.876+3616_876+3617i others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51801947 | |||||
chr15:51802012
|
G | A | 16 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(13): Show | 17 | HG00140.hp2 HG04115.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+3672G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802012 | ||||||
chr15:51802137
|
C | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.876+3797C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802137 | ||||||
chr15:51802152
|
C | T | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.876+3812C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802152 | ||||||
chr15:51802171
|
C | T | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(121): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.876+3831C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802171 | ||||||
chr15:51802219
|
CA | C | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.876+3888delA | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51802219 | |||||
chr15:51802403
|
T | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0244 | 4 | HG01074.hp2 HG01192.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.877-3974T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802403 | ||||||
chr15:51802483
|
G | A | 1 | a0001c0001t0002g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.877-3894G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802483 | ||||||
chr15:51802545
|
G | A | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(121): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.877-3832G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802545 | ||||||
chr15:51802803
|
T | C | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-3574T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802803 | ||||||
chr15:51802928
|
T | C | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(121): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.877-3449T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802928 | ||||||
chr15:51802981
|
A | C | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-3396A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802981 | ||||||
chr15:51802982
|
A | T | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(121): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.877-3395A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51802982 | ||||||
chr15:51803113
|
G | A | 1 | a0001c0001t0016g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.877-3264G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803113 | ||||||
chr15:51803144
|
A | AATTAAAT others(3): Show |
7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-3232_877-3223d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51803144 | |||||
chr15:51803168
|
C | CT | 128 | a0001c0001t0001g0016a0001c0001t0001g0150a0001c0001t0001g0151others(125): Show | 131 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.877-3186dupT | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51803168 | |||||
chr15:51803184
|
T | TC | 98 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(95): Show | 102 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.877-3193_877-3192i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803184 | ||||||
chr15:51803190
|
T | G | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-3187T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803190 | ||||||
chr15:51803190
|
T | TG | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.877-3187_877-3186i others(3): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803190 | ||||||
chr15:51803275
|
G | T | 1 | a0001c0001t0008g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.877-3102G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803275 | ||||||
chr15:51803288
|
C | A | 1 | a0001c0001t0053g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.877-3089C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803288 | ||||||
chr15:51803305
|
T | C | 177 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.877-3072T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803305 | ||||||
chr15:51803381
|
A | G | 1 | a0001c0001t0008g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.877-2996A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803381 | ||||||
chr15:51803396
|
G | T | 1 | a0001c0001t0036g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877-2981G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803396 | ||||||
chr15:51803449
|
G | A | 3 | a0001c0001t0012g0132a0001c0001t0012g0135a0001c0001t0012g0136 | 3 | HG02451.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.877-2928G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803449 | ||||||
chr15:51803511
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.877-2866C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803511 | ||||||
chr15:51803625
|
A | G | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-2752A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803625 | ||||||
chr15:51803880
|
C | T | 1 | a0001c0001t0005g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.877-2497C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803880 | ||||||
chr15:51803952
|
A | G | 3 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341 | 3 | HG00642.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.877-2425A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51803952 | ||||||
chr15:51804027
|
G | A | 1 | a0001c0001t0034g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.877-2350G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804027 | ||||||
chr15:51804116
|
C | T | 1 | a0001c0001t0010g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.877-2261C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804116 | ||||||
chr15:51804153
|
G | T | 2 | a0001c0001t0003g0229a0001c0001t0003g0231 | 2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.877-2224G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804153 | ||||||
chr15:51804181
|
G | T | 1 | a0001c0001t0001g0347 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.877-2196G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804181 | ||||||
chr15:51804194
|
A | T | 2 | a0001c0001t0017g0004a0001c0001t0017g0149 | 3 | HG01167.hp1 HG01169.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.877-2183A>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804194 | ||||||
chr15:51804445
|
A | G | 5 | a0001c0001t0007g0012a0001c0001t0007g0214a0001c0001t0007g0215others(2): Show | 6 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-1932A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804445 | ||||||
chr15:51804460
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1917A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804460 | ||||||
chr15:51804553
|
A | ATGTTT | 10 | a0001c0001t0005g0177a0001c0001t0005g0182a0001c0001t0005g0183others(7): Show | 10 | NA18612.hp1 NA18747.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.877-1824_877-1823i others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804553 | ||||||
chr15:51804554
|
C | T | 26 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(23): Show | 27 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.877-1823C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804554 | ||||||
chr15:51804554
|
CGTTTTGT others(3): Show |
C | 1 | a0001c0001t0002g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.877-1802_877-1793d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804554 | |||||
chr15:51804575
|
GTTTTGTT others(3): Show |
G | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.877-1797_877-1788d others(12): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804575 | |||||
chr15:51804580
|
GTTTTT | G | 13 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(10): Show | 13 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.877-1790_877-1786d others(7): Show |
TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 51804580 | |||||
chr15:51804585
|
T | G | 33 | a0001c0001t0001g0310a0001c0001t0001g0322a0001c0001t0005g0011others(30): Show | 34 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.877-1792T>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804585 | ||||||
chr15:51804601
|
C | T | 295 | a0001c0001t0001g0016a0001c0001t0001g0150a0001c0001t0001g0151others(292): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.877-1776C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804601 | ||||||
chr15:51804665
|
C | T | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.877-1712C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804665 | ||||||
chr15:51804683
|
C | T | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1694C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804683 | ||||||
chr15:51804727
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0033g0002 | 3 | HG02451.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.877-1650C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804727 | ||||||
chr15:51804814
|
G | A | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.877-1563G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804814 | ||||||
chr15:51804896
|
G | A | 1 | a0001c0001t0012g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.877-1481G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51804896 | ||||||
chr15:51805055
|
T | C | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1322T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805055 | ||||||
chr15:51805083
|
C | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02145.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.877-1294C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805083 | ||||||
chr15:51805160
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1217A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805160 | ||||||
chr15:51805179
|
C | A | 1 | a0001c0001t0005g0193 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.877-1198C>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805179 | ||||||
chr15:51805192
|
T | C | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.877-1185T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805192 | ||||||
chr15:51805244
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1133G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805244 | ||||||
chr15:51805272
|
A | C | 1 | a0001c0001t0003g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877-1105A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805272 | ||||||
chr15:51805327
|
A | C | 10 | a0001c0001t0009g0010a0001c0001t0009g0164a0001c0001t0009g0165others(7): Show | 11 | HG00140.hp2 NA18946.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.877-1050A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805327 | ||||||
chr15:51805420
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-957A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805420 | ||||||
chr15:51805683
|
T | C | 1 | a0001c0001t0043g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877-694T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805683 | ||||||
chr15:51805685
|
G | C | 1 | a0001c0001t0007g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.877-692G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805685 | ||||||
chr15:51805904
|
A | G | 1 | a0001c0001t0023g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.877-473A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805904 | ||||||
chr15:51805932
|
T | C | 3 | a0001c0001t0019g0204a0001c0001t0019g0205a0001c0001t0019g0208 | 3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.877-445T>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 8/9 | chr15 | 51805932 | ||||||
chr15:51806692
|
C | T | 1 | a0001c0001t0047g0282 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1021+171C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806692 | ||||||
chr15:51806704
|
T | A | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(124): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1021+183T>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806704 | ||||||
chr15:51806835
|
C | G | 8 | a0001c0001t0009g0010a0001c0001t0009g0166a0001c0001t0009g0169others(5): Show | 9 | NA18946.hp2 NA18957.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1021+314C>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806835 | ||||||
chr15:51806961
|
A | G | 27 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0179others(24): Show | 28 | HG00544.hp1 HG01106.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.1021+440A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51806961 | ||||||
chr15:51807433
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0018g0264others(2): Show | 5 | HG01109.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021+912C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807433 | ||||||
chr15:51807517
|
C | T | 4 | a0001c0001t0012g0132a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-903C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807517 | ||||||
chr15:51807540
|
G | A | 1 | a0001c0001t0017g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1022-880G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807540 | ||||||
chr15:51807562
|
C | T | 3 | a0001c0001t0001g0314a0001c0001t0001g0332a0001c0001t0050g0301 | 3 | HG00609.hp1 HG02523.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1022-858C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807562 | ||||||
chr15:51807808
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-612A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807808 | ||||||
chr15:51807814
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1022-606G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807814 | ||||||
chr15:51807865
|
C | T | 6 | a0001c0001t0013g0143a0001c0001t0013g0145a0001c0001t0013g0146others(3): Show | 6 | HG04115.hp1 NA18747.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-555C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807865 | ||||||
chr15:51807948
|
A | G | 1 | a0001c0001t0002g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1022-472A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807948 | ||||||
chr15:51807949
|
G | T | 1 | a0001c0001t0002g0110 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1022-471G>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807949 | ||||||
chr15:51807978
|
G | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0132a0001c0001t0012g0133others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-442G>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51807978 | ||||||
chr15:51808018
|
C | T | 6 | a0001c0001t0002g0094a0001c0001t0002g0104a0001c0001t0002g0126others(3): Show | 6 | HG00323.hp1 HG00741.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022-402C>T | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808018 | ||||||
chr15:51808094
|
A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(175): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1022-326A>G | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808094 | ||||||
chr15:51808106
|
G | A | 3 | a0001c0001t0002g0080a0001c0001t0028g0078a0001c0001t0031g0079 | 3 | HG01496.hp2 HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1022-314G>A | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808106 | ||||||
chr15:51808223
|
A | C | 229 | a0001c0001t0001g0016a0001c0001t0001g0150a0001c0001t0001g0151others(226): Show | 239 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1022-197A>C | TMOD2 | ENSG00000128872.10 | transcript | ENST00000249700.9 | protein_coding | 9/9 | chr15 | 51808223 |