geneid | 7042 |
---|---|
ensemblid | ENSG00000092969.12 |
hgncid | 11768 |
symbol | TGFB2 |
name | transforming growth factor beta 2 |
refseq_nuc | NM_003238.6 |
refseq_prot | NP_003229.1 |
ensembl_nuc | ENST00000366930.9 |
ensembl_prot | ENSP00000355897.4 |
mane_status | MANE Select |
chr | chr1 |
start | 218345336 |
end | 218444619 |
strand | + |
ver | v1.2 |
region | chr1:218345336-218444619 |
region5000 | chr1:218340336-218449619 |
regionname0 | TGFB2_chr1_218345336_218444619 |
regionname5000 | TGFB2_chr1_218340336_218449619 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 414 | 288 | 82 | 47 | 121 | 6 | 30 | 95 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0002 | 0/0 | 414 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0003 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1245 | 287 | 82 | 47 | 121 | 6 | 29 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
c0002 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
c0003 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
c0004 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4624 | 46 | 9 | 12 | 13 | 2 | 10 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0002 | 0/0 | 4622 | 37 | 2 | 3 | 26 | 1 | 5 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0003 | 0/0 | 4628 | 29 | 11 | 4 | 11 | 0 | 3 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0004 | 0/0 | 4626 | 23 | 4 | 4 | 15 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0005 | 0/1 | 4623 | 9 | 3 | 2 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0006 | 0/0 | 4625 | 8 | 0 | 0 | 6 | 2 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0007 | 0/0 | 4623 | 8 | 0 | 5 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0008 | 0/0 | 4622 | 7 | 0 | 6 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0009 | 0/0 | 4627 | 6 | 1 | 1 | 2 | 0 | 2 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0010 | 0/0 | 4636 | 5 | 0 | 0 | 5 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0011 | 0/0 | 4626 | 4 | 3 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0012 | 0/0 | 4630 | 4 | 0 | 0 | 4 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0013 | 0/0 | 4628 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0014 | 0/0 | 4625 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0015 | 0/0 | 4624 | 3 | 0 | 0 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0016 | 0/0 | 4624 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0017 | 0/0 | 4619 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0018 | 0/0 | 4636 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0019 | 0/0 | 4630 | 3 | 2 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0020 | 0/0 | 4628 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0021 | 0/0 | 4636 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0022 | 0/0 | 4629 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0023 | 0/0 | 4627 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0024 | 0/0 | 4627 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0025 | 0/0 | 4626 | 2 | 0 | 1 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0026 | 0/0 | 4639 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0027 | 0/0 | 4634 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0028 | 0/0 | 4636 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0029 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0030 | 0/0 | 4638 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0031 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0032 | 0/0 | 4628 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0033 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0034 | 1/0 | 4624 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0035 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0036 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0037 | 0/0 | 4630 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0038 | 0/0 | 4625 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0039 | 0/0 | 4629 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0040 | 0/0 | 4628 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0041 | 0/0 | 4628 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0042 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0043 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0044 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0045 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0046 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0047 | 0/0 | 4628 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0048 | 0/0 | 4630 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0049 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0050 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0051 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0052 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0053 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0054 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0055 | 0/0 | 4623 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0056 | 0/0 | 4623 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0057 | 0/0 | 4631 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0058 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0059 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0060 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0061 | 0/0 | 4624 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0062 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0063 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0064 | 0/0 | 4623 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0065 | 0/0 | 4623 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0066 | 0/0 | 4622 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0067 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0068 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0069 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0070 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0071 | 0/0 | 4622 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0072 | 0/0 | 4623 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0073 | 0/0 | 4623 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0074 | 0/0 | 4623 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0075 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0076 | 0/0 | 4640 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0077 | 0/0 | 4639 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0078 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0079 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0080 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0081 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0082 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0083 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0084 | 0/0 | 4628 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0085 | 0/0 | 4628 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0086 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0087 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0088 | 0/0 | 4644 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0089 | 0/0 | 4639 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0090 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
t0091 | 0/0 | 4630 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1245 | 287 | 82 | 47 | 121 | 6 | 29 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0002 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0002c0003 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0003c0004 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5868 | 46 | 9 | 12 | 13 | 2 | 10 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0002 | 0/0 | 5866 | 35 | 2 | 2 | 26 | 1 | 4 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0003 | 0/0 | 5872 | 28 | 11 | 4 | 10 | 0 | 3 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0004 | 0/0 | 5870 | 23 | 4 | 4 | 15 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0005 | 0/1 | 5867 | 9 | 3 | 2 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0006 | 0/0 | 5869 | 8 | 0 | 0 | 6 | 2 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0007 | 0/0 | 5867 | 8 | 0 | 5 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0008 | 0/0 | 5866 | 7 | 0 | 6 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0009 | 0/0 | 5871 | 6 | 1 | 1 | 2 | 0 | 2 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0010 | 0/0 | 5880 | 5 | 0 | 0 | 5 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0011 | 0/0 | 5870 | 4 | 3 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0012 | 0/0 | 5874 | 4 | 0 | 0 | 4 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0013 | 0/0 | 5872 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0014 | 0/0 | 5869 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0015 | 0/0 | 5868 | 3 | 0 | 0 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0016 | 0/0 | 5868 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0017 | 0/0 | 5863 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0018 | 0/0 | 5880 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0019 | 0/0 | 5874 | 3 | 2 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0020 | 0/0 | 5872 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0021 | 0/0 | 5880 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0022 | 0/0 | 5873 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0023 | 0/0 | 5871 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0024 | 0/0 | 5871 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0025 | 0/0 | 5870 | 2 | 0 | 1 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0026 | 0/0 | 5883 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0027 | 0/0 | 5878 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0028 | 0/0 | 5880 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0029 | 0/0 | 5876 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0030 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0031 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0032 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0033 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0034 | 1/0 | 5868 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0035 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0036 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0037 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0038 | 0/0 | 5869 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0039 | 0/0 | 5873 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0040 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0041 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0042 | 0/0 | 5871 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0043 | 0/0 | 5870 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0044 | 0/0 | 5870 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0045 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0046 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0047 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0048 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0049 | 0/0 | 5870 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0050 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0051 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0052 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0053 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0054 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0055 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0056 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0057 | 0/0 | 5875 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0058 | 0/0 | 5868 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0059 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0060 | 0/0 | 5868 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0061 | 0/0 | 5868 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0062 | 0/0 | 5868 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0063 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0064 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0065 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0066 | 0/0 | 5866 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0067 | 0/0 | 5866 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0068 | 0/0 | 5868 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0069 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0070 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0071 | 0/0 | 5866 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0072 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0073 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0074 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0075 | 0/0 | 5866 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0076 | 0/0 | 5884 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0077 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0078 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0079 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0080 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0081 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0082 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0083 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0084 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0085 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0086 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0087 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0088 | 0/0 | 5888 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0089 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0090 | 0/0 | 5881 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0001t0091 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0001c0002t0002 | 0/0 | 5866 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0002c0003t0002 | 0/0 | 5866 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
a0003c0004t0003 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | copy fasta | chr1 | 218340336 | 218449619 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0020g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0021g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0021g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0022g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0022g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0023g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0023g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0024g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0025g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0026g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0026g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0027g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0027g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0028g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0028g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0029g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0029g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0030g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0030g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0031g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0032g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0033g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0034g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0035g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0036g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0037g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0038g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0039g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0040g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0041g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0042g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0043g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0044g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0045g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0046g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0047g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0048g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0049g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0050g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0051g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0052g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0053g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0054g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0055g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0056g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0057g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0058g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0059g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0060g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0061g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0062g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0063g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0064g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0065g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0066g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0067g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0068g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0069g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0070g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0071g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0072g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0073g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0074g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0075g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0076g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0077g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0078g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0079g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0080g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0081g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0082g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0083g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0084g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0085g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0086g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0087g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0088g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0089g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0090g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0091g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0003c0004t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0006 | g0089 | EUR | GBR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00438 | hp2 | a0001 | c0001 | t0022 | g0214 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00639 | hp2 | a0002 | c0003 | t0002 | g0080 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0182 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00741 | hp2 | a0001 | c0001 | t0048 | g0241 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0193 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01081 | hp1 | a0001 | c0001 | t0062 | g0107 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01081 | hp2 | a0001 | c0001 | t0066 | g0134 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0225 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01243 | hp1 | a0001 | c0001 | t0026 | g0279 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0272 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0101 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0078 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0259 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01358 | hp2 | a0001 | c0001 | t0042 | g0247 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01433 | hp1 | a0001 | c0001 | t0025 | g0201 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01433 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01496 | hp1 | a0001 | c0001 | t0049 | g0150 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0192 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01515 | hp1 | a0001 | c0001 | t0044 | g0238 | EUR | IBS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01884 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01891 | hp2 | a0001 | c0001 | t0082 | g0264 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0130 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02055 | hp2 | a0001 | c0001 | t0050 | g0205 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02056 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02080 | hp1 | a0001 | c0001 | t0022 | g0037 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02257 | hp1 | a0001 | c0001 | t0014 | g0174 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02257 | hp2 | a0001 | c0001 | t0085 | g0262 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02258 | hp1 | a0001 | c0001 | t0077 | g0280 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0282 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02273 | hp1 | a0001 | c0001 | t0043 | g0052 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02280 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02293 | hp1 | a0001 | c0001 | t0007 | g0119 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02572 | hp1 | a0001 | c0001 | t0057 | g0141 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02572 | hp2 | a0001 | c0001 | t0073 | g0063 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0185 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02602 | hp2 | a0001 | c0001 | t0015 | g0200 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02615 | hp1 | a0001 | c0001 | t0075 | g0065 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02615 | hp2 | a0001 | c0001 | t0027 | g0269 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0111 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0285 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02717 | hp1 | a0001 | c0001 | t0076 | g0281 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0270 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0221 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02809 | hp1 | a0001 | c0001 | t0019 | g0273 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02809 | hp2 | a0001 | c0001 | t0021 | g0228 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0266 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0212 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0004 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02965 | hp1 | a0001 | c0001 | t0067 | g0120 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02965 | hp2 | a0001 | c0001 | t0074 | g0064 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02970 | hp1 | a0001 | c0001 | t0029 | g0267 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02970 | hp2 | a0001 | c0001 | t0080 | g0263 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03017 | hp1 | a0001 | c0001 | t0061 | g0172 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0038 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03098 | hp1 | a0001 | c0001 | t0036 | g0220 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03130 | hp1 | a0001 | c0001 | t0090 | g0011 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03130 | hp2 | a0001 | c0001 | t0060 | g0060 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03139 | hp1 | a0001 | c0001 | t0086 | g0213 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0211 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03195 | hp1 | a0001 | c0001 | t0078 | g0271 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03195 | hp2 | a0001 | c0001 | t0063 | g0086 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0226 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03225 | hp1 | a0001 | c0001 | t0087 | g0210 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03516 | hp2 | a0001 | c0001 | t0016 | g0062 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03540 | hp1 | a0001 | c0001 | t0028 | g0276 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03669 | hp1 | a0001 | c0001 | t0038 | g0229 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03710 | hp1 | a0001 | c0001 | t0025 | g0202 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04184 | hp1 | a0001 | c0001 | t0071 | g0162 | SAS | BEB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04204 | hp1 | a0001 | c0001 | t0039 | g0041 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04204 | hp2 | a0001 | c0001 | t0041 | g0249 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04228 | hp1 | a0001 | c0001 | t0051 | g0168 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04228 | hp2 | a0001 | c0001 | t0009 | g0034 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18522 | hp1 | a0001 | c0001 | t0081 | g0268 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18612 | hp2 | a0001 | c0001 | t0010 | g0016 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18747 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18940 | hp1 | a0001 | c0001 | t0017 | g0147 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18942 | hp1 | a0001 | c0001 | t0046 | g0230 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18942 | hp2 | a0001 | c0001 | t0023 | g0043 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18946 | hp2 | a0001 | c0001 | t0037 | g0215 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18948 | hp2 | a0001 | c0001 | t0045 | g0046 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18949 | hp2 | a0001 | c0001 | t0009 | g0250 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18952 | hp1 | a0001 | c0001 | t0070 | g0132 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18964 | hp2 | a0001 | c0001 | t0056 | g0177 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18966 | hp2 | a0001 | c0001 | t0058 | g0184 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18967 | hp2 | a0001 | c0001 | t0055 | g0149 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18979 | hp2 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18983 | hp2 | a0001 | c0001 | t0023 | g0231 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18985 | hp2 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18989 | hp2 | a0001 | c0001 | t0017 | g0146 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18991 | hp1 | a0001 | c0001 | t0033 | g0044 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18992 | hp1 | a0001 | c0001 | t0089 | g0010 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18992 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18995 | hp2 | a0001 | c0001 | t0030 | g0009 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18998 | hp1 | a0003 | c0004 | t0003 | g0042 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18998 | hp2 | a0001 | c0001 | t0065 | g0187 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19002 | hp2 | a0001 | c0001 | t0054 | g0186 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19003 | hp1 | a0001 | c0001 | t0015 | g0142 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19003 | hp2 | a0001 | c0001 | t0017 | g0148 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19004 | hp1 | a0001 | c0001 | t0047 | g0050 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19007 | hp2 | a0001 | c0001 | t0024 | g0006 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19011 | hp2 | a0001 | c0001 | t0088 | g0007 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19043 | hp1 | a0001 | c0001 | t0084 | g0286 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19043 | hp2 | a0001 | c0001 | t0064 | g0075 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19057 | hp1 | a0001 | c0001 | t0091 | g0012 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19057 | hp2 | a0001 | c0001 | t0069 | g0104 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19058 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19074 | hp1 | a0001 | c0001 | t0068 | g0171 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19077 | hp1 | a0001 | c0001 | t0072 | g0100 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19080 | hp2 | a0001 | c0001 | t0013 | g0245 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19084 | hp1 | a0001 | c0001 | t0053 | g0058 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19084 | hp2 | a0001 | c0001 | t0030 | g0021 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19087 | hp1 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19088 | hp2 | a0001 | c0001 | t0059 | g0059 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19091 | hp2 | a0001 | c0001 | t0015 | g0135 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19240 | hp2 | a0001 | c0001 | t0028 | g0275 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20129 | hp1 | a0001 | c0001 | t0031 | g0284 | AFR | ASW | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20129 | hp2 | a0001 | c0001 | t0052 | g0055 | AFR | ASW | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0145 | EUR | TSI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | GIH | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20905 | hp2 | a0001 | c0001 | t0040 | g0028 | SAS | GIH | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0278 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0067 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0283 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03471 | hp2 | a0001 | c0001 | t0079 | g0265 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0277 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0260 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20300 | hp2 | a0001 | c0001 | t0035 | g0254 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA21309 | hp2 | a0001 | c0001 | t0083 | g0023 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0164 | REF | REF | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0034 | g0190 | REF | REF | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218346973
|
G | A | 1 | a0002 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.272G>A | p.Arg91His | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1638/5868 | 272/1245 | 91/414 | chr1 | 218346973 | ||
chr1:218441262
|
C | T | 1 | a0003 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ser382Phe | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2511/5868 | 1145/1245 | 382/414 | chr1 | 218441262 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218346815
|
G | A | 1 | a0001c0002 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.114G>A | p.Glu38Glu | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1480/5868 | 114/1245 | 38/414 | chr1 | 218346815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218345400
|
A | G | 7 | a0001c0001t0010a0001c0001t0012a0001c0001t0030others(4): Show | 15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-1302A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1302 | chr1 | 218345400 | |||||
chr1:218345472
|
G | A | 3 | a0001c0001t0020a0001c0001t0031a0001c0001t0032 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1230G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1230 | chr1 | 218345472 | |||||
chr1:218345557
|
G | C | 1 | a0001c0001t0033 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1145G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1145 | chr1 | 218345557 | |||||
chr1:218345686
|
C | T | 3 | a0001c0001t0029a0001c0001t0086a0001c0001t0087 | 4 | HG02886.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1016C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1016 | chr1 | 218345686 | |||||
chr1:218345918
|
A | C | 93 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | 289 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(286): Show |
5_prime_UTR_variant | MODIFIER | c.-784A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 784 | chr1 | 218345918 | |||||
chr1:218345956
|
G | T | 1 | a0001c0001t0085 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-746G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 746 | chr1 | 218345956 | |||||
chr1:218345988
|
A | C | 27 | a0001c0001t0010a0001c0001t0012a0001c0001t0018others(24): Show | 44 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-714A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 714 | chr1 | 218345988 | |||||
chr1:218346025
|
T | C | 52 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(49): Show | 132 | HG00438.hp2 HG00738.hp2 HG01109.hp1 others(129): Show |
5_prime_UTR_variant | MODIFIER | c.-677T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 677 | chr1 | 218346025 | |||||
chr1:218346054
|
A | ACG | 5 | a0001c0001t0020a0001c0001t0031a0001c0001t0032others(2): Show | 6 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-646_-645dupGC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 644 | INFO_REALIGN_3_PRIME | chr1 | 218346054 | ||||
chr1:218346056
|
G | GCA | 11 | a0001c0001t0013a0001c0001t0014a0001c0001t0015others(8): Show | 21 | HG00741.hp2 HG01243.hp2 HG01433.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-622_-621dupAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACA | 4 | a0001c0001t0012a0001c0001t0029a0001c0001t0035others(1): Show | 8 | HG02523.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-624_-621dupACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACACA | 6 | a0001c0001t0027a0001c0001t0078a0001c0001t0080others(3): Show | 7 | HG02615.hp2 HG02717.hp2 HG02970.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-626_-621dupACACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACACAC others(1): Show |
2 | a0001c0001t0018a0001c0001t0079 | 4 | HG02258.hp2 HG02280.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-628_-621dupACACAC others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0010a0001c0001t0028a0001c0001t0090 | 8 | HG02056.hp1 HG03130.hp1 HG03540.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-630_-621dupACACAC others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACACAC others(5): Show |
4 | a0001c0001t0026a0001c0001t0030a0001c0001t0076others(1): Show | 6 | HG01243.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-632_-621dupACACAC others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
G | GCACACAC others(11): Show |
1 | a0001c0001t0088 | 1 | NA19011.hp2 | 5_prime_UTR_variant | MODIFIER | c.-638_-621dupACACAC others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346056
|
GCACA | G | 1 | a0001c0001t0017 | 3 | NA18940.hp1 NA18989.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-624_-621delACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 621 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | ||||
chr1:218346076
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0082 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-621_-620insACGCAC others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346076 | ||||
chr1:218346081
|
C | CACACACA others(6): Show |
1 | a0001c0001t0089 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-621_-620insACACAC others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | chr1 | 218346081 | |||||
chr1:218346082
|
G | A | 2 | a0001c0001t0027a0001c0001t0078 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-620G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | chr1 | 218346082 | |||||
chr1:218346315
|
T | C | 1 | a0001c0001t0080 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-387T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 387 | chr1 | 218346315 | |||||
chr1:218346352
|
C | G | 1 | a0001c0001t0047 | 1 | NA19004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-350C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 350 | chr1 | 218346352 | |||||
chr1:218346414
|
A | T | 4 | a0001c0001t0016a0001c0001t0073a0001c0001t0074others(1): Show | 6 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-288A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 288 | chr1 | 218346414 | |||||
chr1:218346586
|
A | AAAAC | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(50): Show | 133 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-113_-110dupACAA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 109 | INFO_REALIGN_3_PRIME | chr1 | 218346586 | ||||
chr1:218441401
|
G | A | 7 | a0001c0001t0038a0001c0001t0051a0001c0001t0052others(4): Show | 7 | HG03669.hp1 HG04228.hp1 NA18967.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*39G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 39 | chr1 | 218441401 | |||||
chr1:218441427
|
C | T | 1 | a0001c0001t0072 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 65 | chr1 | 218441427 | |||||
chr1:218441496
|
C | CG | 4 | a0001c0001t0036a0001c0001t0039a0001c0001t0057others(1): Show | 4 | HG02572.hp1 HG03098.hp1 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*136dupG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 137 | INFO_REALIGN_3_PRIME | chr1 | 218441496 | ||||
chr1:218441497
|
G | A | 1 | a0001c0001t0056 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 135 | chr1 | 218441497 | |||||
chr1:218441563
|
A | T | 54 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(51): Show | 160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 201 | chr1 | 218441563 | |||||
chr1:218441683
|
G | GACAACAA others(2): Show |
4 | a0001c0001t0021a0001c0001t0050a0001c0001t0057others(1): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*335_*343dupCAACAA others(3): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 344 | INFO_REALIGN_3_PRIME | chr1 | 218441683 | ||||
chr1:218442082
|
T | C | 1 | a0001c0001t0059 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 720 | chr1 | 218442082 | |||||
chr1:218442087
|
G | C | 2 | a0001c0001t0064a0001c0001t0073 | 2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*725G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 725 | chr1 | 218442087 | |||||
chr1:218442109
|
A | C | 64 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(61): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*747A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 747 | chr1 | 218442109 | |||||
chr1:218442146
|
G | A | 1 | a0001c0001t0043 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 784 | chr1 | 218442146 | |||||
chr1:218442150
|
GT | G | 9 | a0001c0001t0021a0001c0001t0038a0001c0001t0050others(6): Show | 10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*799delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 799 | INFO_REALIGN_3_PRIME | chr1 | 218442150 | ||||
chr1:218442331
|
T | C | 1 | a0001c0001t0077 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 969 | chr1 | 218442331 | |||||
chr1:218442343
|
C | G | 1 | a0001c0001t0046 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*981C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 981 | chr1 | 218442343 | |||||
chr1:218442355
|
A | G | 1 | a0001c0001t0045 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 993 | chr1 | 218442355 | |||||
chr1:218442459
|
G | A | 1 | a0001c0001t0040 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1097 | chr1 | 218442459 | |||||
chr1:218442490
|
G | A | 2 | a0001c0001t0049a0001c0001t0060 | 2 | HG01496.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1128G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1128 | chr1 | 218442490 | |||||
chr1:218442583
|
G | C | 1 | a0001c0001t0061 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1221 | chr1 | 218442583 | |||||
chr1:218442672
|
C | T | 64 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(61): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1310 | chr1 | 218442672 | |||||
chr1:218442677
|
T | G | 2 | a0001c0001t0059a0001c0001t0065 | 2 | NA18998.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1315 | chr1 | 218442677 | |||||
chr1:218442751
|
C | T | 1 | a0001c0001t0071 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1389 | chr1 | 218442751 | |||||
chr1:218442805
|
T | A | 4 | a0001c0001t0021a0001c0001t0050a0001c0001t0057others(1): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1443T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1443 | chr1 | 218442805 | |||||
chr1:218442817
|
G | A | 1 | a0001c0001t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1455G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1455 | chr1 | 218442817 | |||||
chr1:218442864
|
T | C | 2 | a0001c0001t0044a0001c0001t0066 | 2 | HG01081.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1502T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1502 | chr1 | 218442864 | |||||
chr1:218442890
|
A | G | 1 | a0001c0001t0024 | 2 | NA19007.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1528A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1528 | chr1 | 218442890 | |||||
chr1:218442947
|
C | G | 2 | a0001c0001t0008a0001c0001t0043 | 8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1585C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1585 | chr1 | 218442947 | |||||
chr1:218442986
|
T | A | 25 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(22): Show | 57 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1624T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1624 | chr1 | 218442986 | |||||
chr1:218443118
|
G | C | 1 | a0001c0001t0051 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1756 | chr1 | 218443118 | |||||
chr1:218443278
|
A | T | 1 | a0001c0001t0070 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1916 | chr1 | 218443278 | |||||
chr1:218443369
|
C | T | 1 | a0001c0001t0069 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2007 | chr1 | 218443369 | |||||
chr1:218443370
|
G | A | 5 | a0001c0001t0007a0001c0001t0023a0001c0001t0024others(2): Show | 14 | HG01258.hp1 HG01496.hp2 HG01928.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2008G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2008 | chr1 | 218443370 | |||||
chr1:218443550
|
T | C | 4 | a0001c0001t0038a0001c0001t0051a0001c0001t0052others(1): Show | 4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2188T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2188 | chr1 | 218443550 | |||||
chr1:218443631
|
T | C | 1 | a0001c0001t0084 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2269 | chr1 | 218443631 | |||||
chr1:218443709
|
G | GT | 2 | a0001c0001t0006a0001c0001t0022 | 10 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2361dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2362 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | ||||
chr1:218443709
|
GT | G | 22 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(19): Show | 49 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2361delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2361 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | ||||
chr1:218443709
|
GTT | G | 42 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(39): Show | 122 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2360_*2361delTT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2360 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | ||||
chr1:218443710
|
T | G | 1 | a0001c0001t0062 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2348T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2348 | chr1 | 218443710 | |||||
chr1:218443793
|
C | G | 64 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(61): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*2431C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2431 | chr1 | 218443793 | |||||
chr1:218443926
|
A | G | 2 | a0001c0001t0038a0001c0001t0053 | 2 | HG03669.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2564A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2564 | chr1 | 218443926 | |||||
chr1:218444201
|
G | A | 58 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(55): Show | 164 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2839G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2839 | chr1 | 218444201 | |||||
chr1:218444312
|
G | A | 1 | a0001c0001t0059 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2950G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2950 | chr1 | 218444312 | |||||
chr1:218444558
|
C | T | 58 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(55): Show | 164 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3196C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 3196 | chr1 | 218444558 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218347160
|
T | C | 2 | a0001c0001t0024g0005a0001c0001t0024g0006 | 2 | NA19007.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.346+113T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347160 | ||||||
chr1:218347245
|
T | G | 15 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+198T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347245 | ||||||
chr1:218347372
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285others(1): Show | 5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+325A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347372 | ||||||
chr1:218347442
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346+395G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347442 | ||||||
chr1:218347457
|
G | A | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+410G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347457 | ||||||
chr1:218347501
|
G | A | 33 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0029others(30): Show | 33 | HG00738.hp2 HG01175.hp2 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.346+454G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347501 | ||||||
chr1:218347579
|
T | C | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+532T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347579 | ||||||
chr1:218347653
|
A | G | 131 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(128): Show | 133 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(130): Show |
intron_variant | MODIFIER | c.346+606A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347653 | ||||||
chr1:218347669
|
T | C | 2 | a0001c0001t0004g0209a0001c0001t0011g0208 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.346+622T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347669 | ||||||
chr1:218347933
|
A | AT | 22 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0003g0053others(19): Show | 22 | HG00738.hp2 HG01169.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.346+904dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218347933 | |||||
chr1:218347933
|
AT | A | 18 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0004g0209others(15): Show | 18 | HG00438.hp2 HG02523.hp2 HG02896.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+904delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218347933 | |||||
chr1:218348080
|
A | AAAAG | 8 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0029g0266others(5): Show | 8 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+1049_346+1052d others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218348080 | |||||
chr1:218348080
|
A | G | 12 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0018g0282others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+1033A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348080 | ||||||
chr1:218348158
|
A | G | 3 | a0001c0001t0002g0204a0001c0001t0005g0203a0001c0001t0050g0205 | 3 | HG02055.hp1 HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.346+1111A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348158 | ||||||
chr1:218348267
|
G | A | 236 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(233): Show | 238 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.346+1220G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348267 | ||||||
chr1:218348379
|
T | C | 1 | a0001c0001t0080g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.346+1332T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348379 | ||||||
chr1:218348522
|
C | T | 1 | a0001c0001t0043g0052 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.346+1475C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348522 | ||||||
chr1:218348756
|
T | C | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+1709T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348756 | ||||||
chr1:218348939
|
A | G | 13 | a0001c0001t0003g0022a0001c0001t0003g0251a0001c0001t0003g0253others(10): Show | 13 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+1892A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348939 | ||||||
chr1:218349126
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0029g0266a0001c0001t0029g0267 | 3 | HG01891.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.346+2079C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349126 | ||||||
chr1:218349220
|
G | C | 2 | a0001c0001t0029g0266a0001c0001t0029g0267 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.346+2173G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349220 | ||||||
chr1:218349244
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160 | 3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.346+2197G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349244 | ||||||
chr1:218349338
|
C | CA | 12 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2299dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218349338 | |||||
chr1:218349344
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.346+2297A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349344 | ||||||
chr1:218349348
|
G | A | 15 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+2301G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349348 | ||||||
chr1:218349364
|
C | A | 1 | a0001c0001t0003g0024 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.346+2317C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349364 | ||||||
chr1:218349683
|
A | G | 25 | a0001c0001t0003g0232a0001c0001t0003g0237a0001c0001t0003g0239others(22): Show | 26 | HG00438.hp2 HG00741.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.346+2636A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349683 | ||||||
chr1:218349705
|
C | A | 16 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+2658C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349705 | ||||||
chr1:218349857
|
G | A | 10 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(7): Show | 10 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+2810G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349857 | ||||||
chr1:218349912
|
T | G | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+2865T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349912 | ||||||
chr1:218349921
|
G | A | 13 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0018g0282others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+2874G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349921 | ||||||
chr1:218350142
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.346+3095A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350142 | ||||||
chr1:218350183
|
C | T | 15 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+3136C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350183 | ||||||
chr1:218350184
|
G | A | 3 | a0001c0001t0002g0057a0001c0001t0002g0163a0001c0001t0071g0162 | 3 | HG03491.hp2 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.346+3137G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350184 | ||||||
chr1:218350206
|
C | G | 3 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+3159C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350206 | ||||||
chr1:218350308
|
G | A | 89 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(86): Show | 91 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.346+3261G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350308 | ||||||
chr1:218350388
|
C | T | 112 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(109): Show | 114 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(111): Show |
intron_variant | MODIFIER | c.346+3341C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350388 | ||||||
chr1:218350637
|
GTTATC | G | 4 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285others(1): Show | 5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+3594_346+3598d others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218350637 | |||||
chr1:218350750
|
T | C | 1 | a0001c0001t0060g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.346+3703T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350750 | ||||||
chr1:218350962
|
A | G | 81 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(78): Show | 83 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.346+3915A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350962 | ||||||
chr1:218350981
|
A | T | 1 | a0001c0001t0085g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+3934A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350981 | ||||||
chr1:218351082
|
T | C | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219 | 3 | HG03225.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.346+4035T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351082 | ||||||
chr1:218351199
|
A | G | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+4152A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351199 | ||||||
chr1:218351290
|
A | G | 238 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(235): Show | 240 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.346+4243A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351290 | ||||||
chr1:218351299
|
T | C | 34 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0029others(31): Show | 34 | HG00738.hp2 HG01175.hp2 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.346+4252T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351299 | ||||||
chr1:218352241
|
C | T | 3 | a0001c0001t0015g0200a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02602.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+5194C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352241 | ||||||
chr1:218352246
|
C | A | 72 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(69): Show | 73 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.346+5199C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352246 | ||||||
chr1:218352262
|
G | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+5215G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352262 | ||||||
chr1:218352392
|
T | A | 2 | a0001c0001t0086g0213a0001c0001t0087g0210 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+5345T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352392 | ||||||
chr1:218352684
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+5637T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352684 | ||||||
chr1:218352716
|
G | A | 7 | a0001c0001t0016g0062a0001c0001t0016g0066a0001c0001t0016g0067others(4): Show | 7 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+5669G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352716 | ||||||
chr1:218352749
|
C | T | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+5702C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352749 | ||||||
chr1:218352886
|
G | C | 72 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0001t0003g0025others(69): Show | 73 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.346+5839G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352886 | ||||||
chr1:218353369
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.346+6322C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353369 | ||||||
chr1:218353402
|
T | G | 1 | a0001c0001t0029g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.346+6355T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353402 | ||||||
chr1:218353471
|
T | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+6424T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353471 | ||||||
chr1:218353498
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.346+6451A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353498 | ||||||
chr1:218353635
|
G | A | 2 | a0001c0001t0021g0221a0001c0001t0036g0220 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.346+6588G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353635 | ||||||
chr1:218353760
|
T | C | 1 | a0001c0001t0082g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+6713T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353760 | ||||||
chr1:218353772
|
C | T | 3 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+6725C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353772 | ||||||
chr1:218353787
|
G | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+6740G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353787 | ||||||
chr1:218353850
|
G | A | 11 | a0001c0001t0004g0209a0001c0001t0011g0208a0001c0001t0013g0211others(8): Show | 11 | HG01243.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+6803G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353850 | ||||||
chr1:218353899
|
C | A | 1 | a0001c0001t0005g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.346+6852C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353899 | ||||||
chr1:218353906
|
A | T | 4 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+6859A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353906 | ||||||
chr1:218354045
|
A | C | 11 | a0001c0001t0003g0022a0001c0001t0003g0253a0001c0001t0003g0255others(8): Show | 11 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+6998A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354045 | ||||||
chr1:218354191
|
A | C | 1 | a0001c0001t0003g0024 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.346+7144A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354191 | ||||||
chr1:218354204
|
C | G | 17 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(14): Show | 17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7157C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354204 | ||||||
chr1:218354214
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+7167T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354214 | ||||||
chr1:218354225
|
G | T | 1 | a0001c0001t0079g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.346+7178G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354225 | ||||||
chr1:218354273
|
C | T | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+7226C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354273 | ||||||
chr1:218354517
|
A | G | 17 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(14): Show | 17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7470A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354517 | ||||||
chr1:218354554
|
G | T | 4 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+7507G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354554 | ||||||
chr1:218354740
|
T | C | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+7693T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354740 | ||||||
chr1:218354745
|
G | A | 17 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(14): Show | 17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7698G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354745 | ||||||
chr1:218354892
|
A | C | 19 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(16): Show | 19 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.346+7845A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354892 | ||||||
chr1:218354987
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.346+7940C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354987 | ||||||
chr1:218355028
|
A | G | 17 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(14): Show | 17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7981A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355028 | ||||||
chr1:218355173
|
T | C | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.346+8126T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355173 | ||||||
chr1:218355577
|
C | T | 21 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(18): Show | 21 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.346+8530C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355577 | ||||||
chr1:218355582
|
G | A | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+8535G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355582 | ||||||
chr1:218355656
|
C | T | 6 | a0001c0001t0004g0209a0001c0001t0011g0208a0001c0001t0013g0211others(3): Show | 6 | HG02809.hp2 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+8609C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355656 | ||||||
chr1:218355838
|
A | T | 4 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+8791A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355838 | ||||||
chr1:218355903
|
A | T | 2 | a0001c0001t0003g0251a0001c0001t0085g0262 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.346+8856A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355903 | ||||||
chr1:218355938
|
A | C | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+8891A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355938 | ||||||
chr1:218355962
|
G | A | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+8915G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355962 | ||||||
chr1:218356000
|
T | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+8953T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356000 | ||||||
chr1:218356111
|
T | C | 2 | a0001c0001t0002g0167a0001c0001t0008g0166 | 2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.346+9064T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356111 | ||||||
chr1:218356224
|
A | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+9177A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356224 | ||||||
chr1:218356244
|
G | A | 3 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+9197G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356244 | ||||||
chr1:218356400
|
G | A | 3 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0074 | 3 | NA18964.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.346+9353G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356400 | ||||||
chr1:218356425
|
T | C | 18 | a0001c0001t0001g0061a0001c0001t0003g0022a0001c0001t0003g0251others(15): Show | 18 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+9378T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356425 | ||||||
chr1:218356519
|
G | A | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+9472G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356519 | ||||||
chr1:218356698
|
G | A | 3 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+9651G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356698 | ||||||
chr1:218356707
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+9660C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356707 | ||||||
chr1:218356848
|
C | T | 20 | a0001c0001t0004g0209a0001c0001t0010g0015a0001c0001t0010g0016others(17): Show | 20 | HG02056.hp1 HG02523.hp2 HG02809.hp2 others(17): Show |
intron_variant | MODIFIER | c.346+9801C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356848 | ||||||
chr1:218356883
|
G | A | 9 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0019g0272others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+9836G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356883 | ||||||
chr1:218357219
|
G | GA | 20 | a0001c0001t0001g0076a0001c0001t0003g0217a0001c0001t0003g0218others(17): Show | 20 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+10187dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357219 | |||||
chr1:218357219
|
GA | G | 6 | a0001c0001t0001g0061a0001c0001t0020g0004a0001c0001t0029g0267others(3): Show | 7 | HG01433.hp2 HG01891.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+10187delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357219 | |||||
chr1:218357227
|
A | G | 11 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0018g0282others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+10180A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357227 | ||||||
chr1:218357305
|
G | C | 3 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271 | 3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+10258G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357305 | ||||||
chr1:218357416
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.346+10369A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357416 | ||||||
chr1:218357418
|
T | A | 3 | a0001c0001t0001g0061a0001c0001t0029g0267a0001c0001t0082g0264 | 3 | HG01891.hp2 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.346+10371T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357418 | ||||||
chr1:218357702
|
T | G | 13 | a0001c0001t0003g0022a0001c0001t0003g0251a0001c0001t0003g0253others(10): Show | 13 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+10655T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357702 | ||||||
chr1:218357807
|
G | C | 1 | a0001c0001t0005g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.346+10760G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357807 | ||||||
chr1:218357820
|
A | T | 4 | a0001c0001t0001g0154a0001c0001t0003g0049a0001c0001t0004g0048others(1): Show | 4 | NA18966.hp1 NA19004.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+10773A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357820 | ||||||
chr1:218357842
|
G | T | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+10795G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357842 | ||||||
chr1:218357902
|
AGTT | A | 5 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0019g0273others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10862_346+1086 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357902 | |||||
chr1:218357929
|
A | G | 5 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0019g0273others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10882A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357929 | ||||||
chr1:218358020
|
C | T | 5 | a0001c0001t0018g0274a0001c0001t0018g0277a0001c0001t0019g0273others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10973C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358020 | ||||||
chr1:218358083
|
G | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+11036G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358083 | ||||||
chr1:218358426
|
T | A | 231 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0076others(228): Show | 233 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.346+11379T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358426 | ||||||
chr1:218358461
|
T | C | 3 | a0001c0001t0026g0278a0001c0001t0026g0279a0001c0001t0077g0280 | 3 | HG01243.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+11414T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358461 | ||||||
chr1:218358504
|
T | C | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+11457T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358504 | ||||||
chr1:218358548
|
C | CT | 40 | a0001c0001t0001g0143a0001c0001t0002g0157a0001c0001t0003g0022others(37): Show | 40 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.346+11519dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218358548 | |||||
chr1:218358557
|
T | C | 1 | a0001c0001t0004g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.346+11510T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358557 | ||||||
chr1:218358572
|
A | G | 216 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0076others(213): Show | 218 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.346+11525A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358572 | ||||||
chr1:218358583
|
C | T | 1 | a0001c0001t0082g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+11536C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358583 | ||||||
chr1:218358628
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.346+11581A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358628 | ||||||
chr1:218358641
|
G | C | 1 | a0001c0001t0007g0088 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.346+11594G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358641 | ||||||
chr1:218358764
|
A | G | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+11717A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358764 | ||||||
chr1:218358790
|
C | T | 4 | a0001c0001t0027g0269a0001c0001t0027g0270a0001c0001t0078g0271others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+11743C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358790 | ||||||
chr1:218358799
|
C | T | 7 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0002g0204others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+11752C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358799 | ||||||
chr1:218358829
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0018g0274a0001c0001t0018g0277others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+11782A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358829 | ||||||
chr1:218358956
|
G | A | 1 | a0001c0001t0004g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.346+11909G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358956 | ||||||
chr1:218358973
|
TGGTCAAG others(15): Show |
T | 2 | a0001c0001t0025g0201a0001c0001t0025g0202 | 2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.346+11927_346+1194 others(26): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358973 | ||||||
chr1:218358996
|
A | T | 2 | a0001c0001t0025g0201a0001c0001t0025g0202 | 2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.346+11949A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358996 | ||||||
chr1:218359116
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.346+12069C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359116 | ||||||
chr1:218359132
|
A | T | 1 | a0001c0001t0016g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346+12085A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359132 | ||||||
chr1:218359181
|
G | C | 12 | a0001c0001t0001g0061a0001c0001t0018g0274a0001c0001t0018g0277others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.346+12134G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359181 | ||||||
chr1:218359310
|
G | T | 3 | a0001c0001t0026g0278a0001c0001t0026g0279a0001c0001t0077g0280 | 3 | HG01243.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+12263G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359310 | ||||||
chr1:218359421
|
C | T | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+12374C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359421 | ||||||
chr1:218359430
|
C | T | 2 | a0001c0001t0009g0250a0001c0001t0021g0221 | 2 | HG02723.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.346+12383C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359430 | ||||||
chr1:218359680
|
G | T | 5 | a0001c0001t0018g0282a0001c0001t0019g0283a0001c0001t0026g0278others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+12633G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359680 | ||||||
chr1:218360025
|
C | A | 2 | a0001c0001t0079g0265a0001c0001t0084g0286 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.346+12978C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360025 | ||||||
chr1:218360234
|
T | C | 1 | a0001c0001t0021g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.346+13187T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360234 | ||||||
chr1:218360301
|
C | T | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+13254C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360301 | ||||||
chr1:218360477
|
C | T | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+13430C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360477 | ||||||
chr1:218360478
|
G | A | 9 | a0001c0001t0001g0061a0001c0001t0018g0274a0001c0001t0018g0277others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+13431G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360478 | ||||||
chr1:218360616
|
G | A | 1 | a0001c0001t0025g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.346+13569G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360616 | ||||||
chr1:218360658
|
C | T | 18 | a0001c0001t0001g0061a0001c0001t0003g0251a0001c0001t0003g0253others(15): Show | 18 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+13611C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360658 | ||||||
chr1:218360805
|
G | A | 4 | a0001c0001t0018g0282a0001c0001t0019g0283a0001c0001t0026g0278others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+13758G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360805 | ||||||
chr1:218360855
|
A | AT | 6 | a0001c0001t0004g0047a0001c0001t0016g0062a0001c0001t0016g0066others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+13816dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218360855 | |||||
chr1:218360865
|
C | G | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+13818C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360865 | ||||||
chr1:218360957
|
C | A | 5 | a0001c0001t0004g0209a0001c0001t0011g0208a0001c0001t0013g0211others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+13910C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360957 | ||||||
chr1:218361120
|
T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346+14073T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361120 | ||||||
chr1:218361194
|
A | G | 5 | a0001c0001t0003g0227a0001c0001t0018g0282a0001c0001t0019g0283others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+14147A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361194 | ||||||
chr1:218361366
|
C | A | 1 | a0001c0001t0046g0230 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.346+14319C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361366 | ||||||
chr1:218361461
|
C | T | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+14414C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361461 | ||||||
chr1:218361513
|
G | A | 1 | a0001c0001t0006g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.346+14466G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361513 | ||||||
chr1:218361636
|
C | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.346+14589C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361636 | ||||||
chr1:218361648
|
T | C | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+14601T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361648 | ||||||
chr1:218361817
|
G | C | 3 | a0001c0001t0003g0227a0001c0001t0026g0278a0001c0001t0026g0279 | 3 | HG01109.hp1 HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+14770G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361817 | ||||||
chr1:218361923
|
T | A | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+14876T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361923 | ||||||
chr1:218361950
|
G | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+14903G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361950 | ||||||
chr1:218362267
|
T | G | 1 | a0001c0001t0003g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.346+15220T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362267 | ||||||
chr1:218362337
|
C | T | 17 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(14): Show | 18 | HG01433.hp2 HG02056.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+15290C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362337 | ||||||
chr1:218362423
|
C | G | 1 | a0001c0001t0004g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.346+15376C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362423 | ||||||
chr1:218362476
|
G | A | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+15429G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362476 | ||||||
chr1:218362573
|
A | G | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+15526A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362573 | ||||||
chr1:218362621
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.346+15574C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362621 | ||||||
chr1:218362712
|
C | T | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+15665C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362712 | ||||||
chr1:218362843
|
G | T | 1 | a0001c0001t0041g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15796G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362843 | ||||||
chr1:218362846
|
T | G | 1 | a0001c0001t0041g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15799T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362846 | ||||||
chr1:218362861
|
A | G | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+15814A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362861 | ||||||
chr1:218362862
|
G | A | 1 | a0001c0001t0041g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15815G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362862 | ||||||
chr1:218363074
|
T | C | 1 | a0001c0001t0003g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.346+16027T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363074 | ||||||
chr1:218363501
|
G | A | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+16454G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363501 | ||||||
chr1:218363519
|
T | C | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+16472T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363519 | ||||||
chr1:218363580
|
A | C | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+16533A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363580 | ||||||
chr1:218363597
|
C | A | 1 | a0001c0001t0006g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.346+16550C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363597 | ||||||
chr1:218363663
|
T | C | 2 | a0001c0001t0002g0091a0001c0001t0015g0142 | 2 | NA18943.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.346+16616T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363663 | ||||||
chr1:218363913
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+16866C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363913 | ||||||
chr1:218363947
|
G | A | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+16900G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363947 | ||||||
chr1:218363968
|
T | C | 128 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0154others(125): Show | 130 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.346+16921T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363968 | ||||||
chr1:218364290
|
T | C | 2 | a0001c0001t0003g0053a0001c0001t0003g0054 | 2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.346+17243T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364290 | ||||||
chr1:218364410
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.346+17363G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364410 | ||||||
chr1:218364450
|
C | T | 1 | a0001c0001t0002g0138 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.346+17403C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364450 | ||||||
chr1:218364480
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.346+17433C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364480 | ||||||
chr1:218364517
|
A | T | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+17470A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364517 | ||||||
chr1:218364584
|
T | C | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+17537T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364584 | ||||||
chr1:218364719
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.346+17672A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364719 | ||||||
chr1:218364754
|
A | C | 1 | a0001c0001t0082g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+17707A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364754 | ||||||
chr1:218364786
|
A | C | 2 | a0001c0001t0027g0269a0001c0001t0027g0270 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+17739A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364786 | ||||||
chr1:218364791
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+17744G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364791 | ||||||
chr1:218364806
|
C | G | 30 | a0001c0001t0001g0061a0001c0001t0010g0015a0001c0001t0010g0016others(27): Show | 31 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.346+17759C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364806 | ||||||
chr1:218364945
|
T | C | 1 | a0001c0001t0068g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.346+17898T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364945 | ||||||
chr1:218365023
|
C | G | 3 | a0001c0001t0001g0136a0001c0001t0002g0137a0001c0001t0015g0135 | 3 | HG00558.hp1 NA18979.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.346+17976C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365023 | ||||||
chr1:218365096
|
C | T | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+18049C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365096 | ||||||
chr1:218365118
|
C | T | 19 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(16): Show | 19 | HG02056.hp1 HG02523.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.346+18071C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365118 | ||||||
chr1:218365431
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0026g0279 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+18384G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365431 | ||||||
chr1:218365664
|
A | AT | 34 | a0001c0001t0001g0084a0001c0001t0001g0124a0001c0001t0001g0128others(31): Show | 34 | HG00558.hp1 HG00621.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.346+18632dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | |||||
chr1:218365664
|
A | ATTTT | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+18629_346+1863 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | |||||
chr1:218365664
|
AT | A | 12 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0005g0203others(9): Show | 13 | HG01109.hp1 HG01433.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+18632delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | |||||
chr1:218365741
|
G | A | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+18694G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365741 | ||||||
chr1:218365898
|
G | C | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.346+18851G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365898 | ||||||
chr1:218365957
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0026g0279 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+18910G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365957 | ||||||
chr1:218366054
|
A | G | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+19007A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366054 | ||||||
chr1:218366135
|
G | A | 1 | a0001c0001t0082g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+19088G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366135 | ||||||
chr1:218366360
|
G | A | 1 | a0001c0001t0061g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+19313G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366360 | ||||||
chr1:218366405
|
G | C | 18 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(15): Show | 18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19358G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366405 | ||||||
chr1:218366445
|
C | T | 18 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(15): Show | 18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19398C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366445 | ||||||
chr1:218366483
|
A | T | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+19436A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366483 | ||||||
chr1:218366484
|
A | T | 1 | a0001c0001t0066g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.346+19437A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366484 | ||||||
chr1:218366615
|
G | A | 4 | a0001c0001t0026g0278a0001c0001t0026g0279a0001c0001t0027g0269others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+19568G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366615 | ||||||
chr1:218366715
|
G | A | 18 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(15): Show | 18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19668G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366715 | ||||||
chr1:218366907
|
C | T | 1 | a0001c0001t0004g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.346+19860C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366907 | ||||||
chr1:218367075
|
C | A | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+20028C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367075 | ||||||
chr1:218367079
|
T | C | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+20032T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367079 | ||||||
chr1:218367113
|
G | A | 21 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(18): Show | 21 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+20066G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367113 | ||||||
chr1:218367125
|
C | T | 18 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(15): Show | 18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+20078C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367125 | ||||||
chr1:218367291
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.346+20244G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367291 | ||||||
chr1:218367379
|
T | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.346+20332T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367379 | ||||||
chr1:218367522
|
G | A | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.346+20475G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367522 | ||||||
chr1:218367549
|
A | G | 13 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0255others(10): Show | 13 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+20502A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367549 | ||||||
chr1:218367792
|
AT | A | 4 | a0001c0001t0001g0152a0001c0001t0017g0146a0001c0001t0017g0147others(1): Show | 4 | NA18940.hp1 NA18989.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+20753delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218367792 | |||||
chr1:218367864
|
T | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346+20817T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367864 | ||||||
chr1:218367891
|
C | T | 2 | a0001c0001t0030g0009a0001c0001t0089g0010 | 2 | NA18992.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.346+20844C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367891 | ||||||
chr1:218367898
|
G | A | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+20851G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367898 | ||||||
chr1:218368365
|
A | G | 133 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0154others(130): Show | 135 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.346+21318A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368365 | ||||||
chr1:218368366
|
A | C | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+21319A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368366 | ||||||
chr1:218368647
|
T | C | 1 | a0001c0001t0091g0012 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.346+21600T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368647 | ||||||
chr1:218368650
|
T | C | 66 | a0001c0001t0001g0093a0001c0001t0001g0154a0001c0001t0001g0169others(63): Show | 67 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.346+21603T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368650 | ||||||
chr1:218368717
|
T | G | 133 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0154others(130): Show | 135 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.346+21670T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368717 | ||||||
chr1:218368724
|
GA | G | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21678delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368724 | ||||||
chr1:218368805
|
G | A | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21758G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368805 | ||||||
chr1:218368943
|
A | G | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21896A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368943 | ||||||
chr1:218368965
|
T | C | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+21918T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368965 | ||||||
chr1:218368978
|
C | T | 3 | a0001c0001t0013g0211a0001c0001t0013g0212a0001c0001t0021g0228 | 3 | HG02809.hp2 HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.346+21931C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368978 | ||||||
chr1:218369027
|
C | T | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21980C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369027 | ||||||
chr1:218369136
|
T | C | 1 | a0001c0001t0002g0173 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.346+22089T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369136 | ||||||
chr1:218369181
|
G | A | 2 | a0001c0001t0027g0269a0001c0001t0027g0270 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22134G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369181 | ||||||
chr1:218369250
|
G | A | 2 | a0001c0001t0027g0269a0001c0001t0027g0270 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22203G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369250 | ||||||
chr1:218369256
|
G | GA | 42 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0084others(39): Show | 43 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.346+22246dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
G | GAA | 6 | a0001c0001t0001g0175a0001c0001t0002g0173a0001c0001t0006g0072others(3): Show | 6 | HG02257.hp1 HG03239.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22245_346+2224 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GA | G | 33 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0085others(30): Show | 33 | HG00621.hp1 HG01081.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.346+22246delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAA | G | 6 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0011g0208others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22243_346+2224 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA | G | 17 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(14): Show | 17 | HG02056.hp1 HG02486.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+22240_346+2224 others(11): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(1): Show |
G | 12 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(9): Show | 12 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+22239_346+2224 others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(2): Show |
G | 17 | a0001c0001t0003g0049a0001c0001t0003g0232a0001c0001t0003g0251others(14): Show | 17 | HG00438.hp2 HG01261.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+22238_346+2224 others(13): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(3): Show |
G | 59 | a0001c0001t0001g0093a0001c0001t0001g0154a0001c0001t0001g0169others(56): Show | 60 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.346+22237_346+2224 others(14): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0003g0246a0001c0001t0033g0044a0001c0001t0037g0215 | 3 | NA18943.hp2 NA18946.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.346+22236_346+2224 others(15): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(5): Show |
G | 3 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285 | 4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+22235_346+2224 others(16): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0025g0202a0001c0001t0050g0205 | 2 | HG02055.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.346+22233_346+2224 others(18): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(12): Show |
G | 2 | a0001c0001t0027g0269a0001c0001t0027g0270 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22228_346+2224 others(23): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(13): Show |
G | 4 | a0001c0001t0001g0061a0001c0001t0018g0277a0001c0001t0019g0273others(1): Show | 4 | HG01891.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+22227_346+2224 others(24): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369256
|
GAAAAAAA others(14): Show |
G | 2 | a0001c0001t0003g0025a0001c0001t0081g0268 | 2 | HG03490.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.346+22226_346+2224 others(25): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | |||||
chr1:218369262
|
A | G | 1 | a0001c0001t0021g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.346+22215A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369262 | ||||||
chr1:218369291
|
A | G | 20 | a0001c0001t0003g0227a0001c0001t0010g0015a0001c0001t0010g0016others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+22244A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369291 | ||||||
chr1:218369319
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346+22272A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369319 | ||||||
chr1:218369328
|
T | G | 1 | a0001c0001t0021g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.346+22281T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369328 | ||||||
chr1:218369508
|
A | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0002g0204others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22461A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369508 | ||||||
chr1:218369513
|
T | G | 3 | a0001c0001t0030g0009a0001c0001t0088g0007a0001c0001t0089g0010 | 3 | NA18992.hp1 NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.346+22466T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369513 | ||||||
chr1:218369534
|
C | T | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+22487C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369534 | ||||||
chr1:218369641
|
C | T | 2 | a0001c0001t0018g0282a0001c0001t0019g0283 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+22594C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369641 | ||||||
chr1:218369650
|
G | A | 1 | a0001c0001t0038g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.346+22603G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369650 | ||||||
chr1:218369670
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.346+22623G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369670 | ||||||
chr1:218369969
|
G | T | 16 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(13): Show | 16 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+22922G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369969 | ||||||
chr1:218370076
|
G | A | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.346+23029G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370076 | ||||||
chr1:218370689
|
C | T | 6 | a0001c0001t0001g0102a0001c0001t0001g0206a0001c0001t0002g0118others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+23642C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370689 | ||||||
chr1:218370735
|
G | A | 3 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0011g0208 | 3 | HG01109.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.346+23688G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370735 | ||||||
chr1:218370780
|
A | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346+23733A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370780 | ||||||
chr1:218370876
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.346+23829G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370876 | ||||||
chr1:218370920
|
G | A | 1 | a0001c0001t0014g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.346+23873G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370920 | ||||||
chr1:218371068
|
G | A | 24 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(21): Show | 24 | HG01109.hp2 HG01261.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.346+24021G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371068 | ||||||
chr1:218371249
|
C | T | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+24202C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371249 | ||||||
chr1:218371309
|
C | A | 1 | a0001c0001t0082g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+24262C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371309 | ||||||
chr1:218371313
|
A | C | 16 | a0001c0001t0004g0026a0001c0001t0005g0203a0001c0001t0014g0196others(13): Show | 16 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+24266A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371313 | ||||||
chr1:218371753
|
T | G | 46 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(43): Show | 46 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.346+24706T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371753 | ||||||
chr1:218371835
|
A | G | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+24788A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371835 | ||||||
chr1:218371937
|
C | T | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+24890C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371937 | ||||||
chr1:218372091
|
A | C | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.346+25044A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372091 | ||||||
chr1:218372391
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0017g0146a0001c0001t0017g0147others(1): Show | 4 | NA18940.hp1 NA18989.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+25344G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372391 | ||||||
chr1:218372427
|
T | G | 6 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0011g0208others(3): Show | 6 | HG01109.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+25380T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372427 | ||||||
chr1:218372482
|
A | G | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346+25435A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372482 | ||||||
chr1:218372828
|
A | C | 136 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(133): Show | 138 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.346+25781A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372828 | ||||||
chr1:218372829
|
C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.346+25782C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372829 | ||||||
chr1:218372848
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0052g0055a0001c0001t0067g0120 | 3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.346+25801G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372848 | ||||||
chr1:218372894
|
C | T | 15 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02523.hp2 NA18522.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+25847C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372894 | ||||||
chr1:218373040
|
TG | T | 7 | a0001c0001t0001g0061a0001c0001t0018g0277a0001c0001t0019g0273others(4): Show | 7 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+25995delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218373040 | |||||
chr1:218373048
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.346+26001C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373048 | ||||||
chr1:218373093
|
G | A | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+26046G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373093 | ||||||
chr1:218373132
|
C | T | 2 | a0001c0001t0018g0274a0001c0001t0025g0201 | 2 | HG01433.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.346+26085C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373132 | ||||||
chr1:218373149
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+26102C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373149 | ||||||
chr1:218373159
|
A | T | 19 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(16): Show | 19 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.346+26112A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373159 | ||||||
chr1:218373266
|
G | T | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+26219G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373266 | ||||||
chr1:218373312
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.346+26265A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373312 | ||||||
chr1:218373466
|
T | C | 24 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(21): Show | 24 | HG01109.hp2 HG01261.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.346+26419T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373466 | ||||||
chr1:218373613
|
G | A | 10 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0011g0208others(7): Show | 10 | HG01109.hp1 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+26566G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373613 | ||||||
chr1:218373676
|
C | CTA | 10 | a0001c0001t0003g0227a0001c0001t0004g0209a0001c0001t0011g0208others(7): Show | 10 | HG01109.hp1 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+26631_346+2663 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218373676 | |||||
chr1:218373739
|
T | A | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346+26692T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373739 | ||||||
chr1:218373835
|
A | T | 16 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(13): Show | 16 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+26788A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373835 | ||||||
chr1:218374129
|
A | T | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+27082A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374129 | ||||||
chr1:218374156
|
T | C | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+27109T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374156 | ||||||
chr1:218374265
|
G | A | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+27218G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374265 | ||||||
chr1:218374329
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.346+27282T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374329 | ||||||
chr1:218374540
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+27493C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374540 | ||||||
chr1:218374643
|
T | C | 1 | a0001c0001t0031g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346+27596T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374643 | ||||||
chr1:218375073
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0018g0277a0001c0001t0019g0273others(3): Show | 6 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+28026G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375073 | ||||||
chr1:218375092
|
C | T | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.346+28045C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375092 | ||||||
chr1:218375179
|
C | T | 64 | a0001c0001t0001g0093a0001c0001t0001g0154a0001c0001t0001g0169others(61): Show | 65 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.346+28132C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375179 | ||||||
chr1:218375183
|
G | T | 2 | a0001c0001t0003g0244a0001c0001t0013g0245 | 2 | NA19011.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.346+28136G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375183 | ||||||
chr1:218375184
|
G | A | 5 | a0001c0001t0003g0232a0001c0001t0003g0237a0001c0001t0004g0235others(2): Show | 5 | HG01928.hp2 NA18747.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+28137G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375184 | ||||||
chr1:218375382
|
G | A | 1 | a0001c0001t0061g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+28335G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375382 | ||||||
chr1:218375407
|
C | CT | 114 | a0001c0001t0001g0093a0001c0001t0001g0154a0001c0001t0001g0169others(111): Show | 116 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.346+28372dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375407 | |||||
chr1:218375438
|
T | TA | 73 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0096others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.346+28403dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375438 | |||||
chr1:218375438
|
T | TAA | 8 | a0001c0001t0001g0061a0001c0001t0004g0003a0001c0001t0018g0277others(5): Show | 9 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+28402_346+2840 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375438 | |||||
chr1:218375451
|
C | A | 13 | a0001c0001t0001g0061a0001c0001t0003g0217a0001c0001t0003g0218others(10): Show | 13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+28404C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375451 | ||||||
chr1:218375554
|
A | G | 1 | a0001c0001t0061g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+28507A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375554 | ||||||
chr1:218375716
|
C | T | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+28669C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375716 | ||||||
chr1:218375800
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0175a0001c0001t0002g0178others(5): Show | 9 | HG02602.hp1 HG03239.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+28753T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375800 | ||||||
chr1:218375863
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0026g0279 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+28816G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375863 | ||||||
chr1:218375894
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0018g0277a0001c0001t0019g0273others(2): Show | 5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+28847C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375894 | ||||||
chr1:218375960
|
A | C | 1 | a0001c0001t0022g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.346+28913A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375960 | ||||||
chr1:218376012
|
A | T | 64 | a0001c0001t0001g0093a0001c0001t0001g0154a0001c0001t0001g0169others(61): Show | 65 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.346+28965A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376012 | ||||||
chr1:218376015
|
G | A | 3 | a0001c0001t0004g0235a0001c0001t0018g0282a0001c0001t0019g0283 | 3 | HG01928.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+28968G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376015 | ||||||
chr1:218376061
|
T | C | 3 | a0001c0001t0003g0227a0001c0001t0026g0278a0001c0001t0026g0279 | 3 | HG01109.hp1 HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+29014T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376061 | ||||||
chr1:218376102
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0018g0277a0001c0001t0019g0273others(3): Show | 6 | HG01243.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+29055C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376102 | ||||||
chr1:218376309
|
C | T | 1 | a0001c0001t0005g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.347-28860C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376309 | ||||||
chr1:218376361
|
A | T | 11 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-28808A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376361 | ||||||
chr1:218376618
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0026g0279 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.347-28551C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376618 | ||||||
chr1:218376824
|
A | T | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.347-28345A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376824 | ||||||
chr1:218376868
|
A | G | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-28301A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376868 | ||||||
chr1:218376919
|
G | A | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-28250G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376919 | ||||||
chr1:218377070
|
A | AG | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-28099_347-2809 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377070 | ||||||
chr1:218377074
|
A | T | 26 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(23): Show | 27 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.347-28095A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377074 | ||||||
chr1:218377144
|
C | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-28025C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377144 | ||||||
chr1:218377165
|
C | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.347-28004C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377165 | ||||||
chr1:218377166
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-28003G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377166 | ||||||
chr1:218377366
|
G | C | 14 | a0001c0001t0010g0015a0001c0001t0010g0016a0001c0001t0010g0018others(11): Show | 14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-27803G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377366 | ||||||
chr1:218377666
|
T | G | 52 | a0001c0001t0001g0076a0001c0001t0001g0097a0001c0001t0001g0102others(49): Show | 52 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.347-27503T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377666 | ||||||
chr1:218377681
|
C | T | 5 | a0001c0001t0003g0256a0001c0001t0003g0257a0001c0001t0003g0258others(2): Show | 5 | HG01261.hp2 HG02145.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-27488C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377681 | ||||||
chr1:218377687
|
C | T | 13 | a0001c0001t0002g0091a0001c0001t0010g0015a0001c0001t0010g0016others(10): Show | 13 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-27482C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377687 | ||||||
chr1:218377771
|
G | C | 10 | a0001c0001t0013g0211a0001c0001t0013g0212a0001c0001t0018g0277others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-27398G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377771 | ||||||
chr1:218377789
|
A | G | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.347-27380A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377789 | ||||||
chr1:218377856
|
C | G | 6 | a0001c0001t0004g0209a0001c0001t0011g0208a0001c0001t0020g0004others(3): Show | 7 | HG01433.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-27313C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377856 | ||||||
chr1:218377931
|
G | A | 10 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0003g0256others(7): Show | 10 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-27238G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377931 | ||||||
chr1:218377955
|
AGTGT | A | 4 | a0001c0001t0020g0004a0001c0001t0031g0284a0001c0001t0032g0285others(1): Show | 5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-27211_347-2720 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377955 | |||||
chr1:218377958
|
G | GTGTT | 8 | a0001c0001t0002g0094a0001c0001t0003g0053a0001c0001t0003g0054others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-27181_347-2717 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | |||||
chr1:218377958
|
GTGTT | G | 34 | a0001c0001t0002g0092a0001c0001t0002g0137a0001c0001t0003g0253others(31): Show | 34 | HG00438.hp1 HG00558.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-27181_347-2717 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | |||||
chr1:218377958
|
GTGTTTGT others(1): Show |
G | 9 | a0001c0001t0013g0211a0001c0001t0013g0212a0001c0001t0018g0277others(6): Show | 9 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-27185_347-2717 others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | |||||
chr1:218377958
|
GTGTTTGT others(9): Show |
G | 1 | a0001c0001t0015g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.347-27193_347-2717 others(20): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | |||||
chr1:218377960
|
GT | G | 3 | a0001c0001t0076g0281a0001c0001t0086g0213a0001c0001t0087g0210 | 3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.347-27206delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377960 | |||||
chr1:218377986
|
T | C | 2 | a0001c0001t0018g0282a0001c0001t0019g0283 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.347-27183T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377986 | ||||||
chr1:218377996
|
T | G | 9 | a0001c0001t0013g0211a0001c0001t0013g0212a0001c0001t0018g0277others(6): Show | 9 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-27173T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377996 | ||||||
chr1:218378121
|
C | A | 61 | a0001c0001t0001g0093a0001c0001t0001g0124a0001c0001t0002g0094others(58): Show | 62 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.347-27048C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378121 | ||||||
chr1:218378132
|
T | A | 1 | a0001c0001t0022g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.347-27037T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378132 | ||||||
chr1:218378148
|
G | GATTT | 5 | a0001c0001t0001g0114a0001c0001t0015g0200a0001c0001t0025g0202others(2): Show | 5 | HG02572.hp1 HG02602.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-26983_347-2698 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | |||||
chr1:218378148
|
GATTT | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0117a0001c0001t0001g0143others(3): Show | 6 | HG00558.hp1 HG01071.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-26983_347-2698 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | |||||
chr1:218378148
|
GATTTATT others(9): Show |
G | 3 | a0001c0001t0001g0169a0001c0001t0051g0168a0002c0003t0002g0080 | 3 | HG00140.hp2 HG00639.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.347-26995_347-2698 others(20): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | |||||
chr1:218378148
|
GATTTATT others(13): Show |
G | 155 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(152): Show | 156 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.347-26999_347-2698 others(24): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | |||||
chr1:218378152
|
T | G | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.347-27017T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378152 | ||||||
chr1:218378159
|
TTATTTAT others(11): Show |
T | 4 | a0001c0001t0004g0027a0001c0001t0023g0043a0001c0001t0045g0046others(1): Show | 4 | NA18942.hp2 NA18948.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-27008_347-2699 others(22): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378159 | |||||
chr1:218378239
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0163 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.347-26930C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378239 | ||||||
chr1:218378245
|
T | C | 159 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(156): Show | 160 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.347-26924T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378245 | ||||||
chr1:218378271
|
G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-26898G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378271 | ||||||
chr1:218378297
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.347-26872C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378297 | ||||||
chr1:218378356
|
T | C | 47 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0124others(44): Show | 47 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.347-26813T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378356 | ||||||
chr1:218378384
|
C | G | 2 | a0001c0001t0060g0060a0001c0001t0066g0134 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.347-26785C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378384 | ||||||
chr1:218378385
|
C | A | 4 | a0001c0001t0019g0272a0001c0001t0026g0278a0001c0001t0028g0275others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-26784C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378385 | ||||||
chr1:218378432
|
C | A | 46 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0093others(43): Show | 46 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.347-26737C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378432 | ||||||
chr1:218378454
|
G | A | 1 | a0001c0001t0005g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.347-26715G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378454 | ||||||
chr1:218378736
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(114): Show | 120 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.347-26433C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378736 | ||||||
chr1:218378773
|
G | GT | 214 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(211): Show | 218 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.347-26386dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378773 | |||||
chr1:218378773
|
G | GTT | 16 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0232others(13): Show | 16 | HG01243.hp2 HG01261.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.347-26387_347-2638 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378773 | |||||
chr1:218378932
|
G | A | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26237G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378932 | ||||||
chr1:218378945
|
T | C | 28 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0159others(25): Show | 28 | HG01109.hp1 HG01169.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-26224T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378945 | ||||||
chr1:218378948
|
C | T | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-26221C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378948 | ||||||
chr1:218378978
|
C | A | 21 | a0001c0001t0001g0061a0001c0001t0002g0091a0001c0001t0002g0121others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-26191C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378978 | ||||||
chr1:218379113
|
A | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(165): Show | 172 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.347-26056A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379113 | ||||||
chr1:218379122
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-26047C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379122 | ||||||
chr1:218379126
|
C | CT | 3 | a0001c0001t0004g0048a0001c0001t0008g0099a0001c0001t0025g0202 | 3 | HG03710.hp1 NA18966.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.347-26040dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | |||||
chr1:218379126
|
C | CTT | 154 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(151): Show | 158 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.347-26041_347-2604 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | |||||
chr1:218379126
|
C | CTTT | 10 | a0001c0001t0001g0096a0001c0001t0003g0025a0001c0001t0006g0073others(7): Show | 10 | HG00738.hp1 HG02293.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-26042_347-2604 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | |||||
chr1:218379130
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(165): Show | 172 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.347-26039C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379130 | ||||||
chr1:218379133
|
T | TC | 4 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-26036_347-2603 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379133 | ||||||
chr1:218379134
|
T | C | 31 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0105others(28): Show | 31 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.347-26035T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379134 | ||||||
chr1:218379143
|
C | T | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26026C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379143 | ||||||
chr1:218379150
|
A | T | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26019A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379150 | ||||||
chr1:218379169
|
G | C | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-26000G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379169 | ||||||
chr1:218379172
|
A | T | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-25997A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379172 | ||||||
chr1:218379187
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-25982C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379187 | ||||||
chr1:218379193
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0102others(58): Show | 63 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.347-25976T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379193 | ||||||
chr1:218379196
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-25973G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379196 | ||||||
chr1:218379201
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0081others(177): Show | 183 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.347-25968C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379201 | ||||||
chr1:218379213
|
A | G | 1 | a0001c0001t0071g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.347-25956A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379213 | ||||||
chr1:218379228
|
G | C | 28 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0105others(25): Show | 28 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-25941G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379228 | ||||||
chr1:218379242
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0085others(122): Show | 128 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-25927C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379242 | ||||||
chr1:218379324
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0002g0094a0001c0001t0006g0089others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-25845A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379324 | ||||||
chr1:218379383
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(210): Show | 217 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-25786C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379383 | ||||||
chr1:218379387
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(210): Show | 217 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-25782G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379387 | ||||||
chr1:218379429
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.347-25740C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379429 | ||||||
chr1:218379430
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0197a0001c0001t0003g0030others(1): Show | 4 | HG02004.hp1 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-25739G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379430 | ||||||
chr1:218379487
|
C | CTT | 65 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0077others(62): Show | 67 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-25669_347-2566 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | |||||
chr1:218379487
|
C | CTTT | 85 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0102others(82): Show | 87 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.347-25670_347-2566 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | |||||
chr1:218379487
|
C | CTTTCTT | 15 | a0001c0001t0002g0091a0001c0001t0002g0121a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02165.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-25679_347-2567 others(10): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | |||||
chr1:218379487
|
C | CTTTT | 29 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0105others(26): Show | 29 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.347-25671_347-2566 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | |||||
chr1:218379575
|
T | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-25594T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379575 | ||||||
chr1:218379629
|
T | C | 1 | a0001c0001t0010g0015 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.347-25540T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379629 | ||||||
chr1:218379699
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0075g0065 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.347-25470A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379699 | ||||||
chr1:218379955
|
A | G | 45 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0105others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.347-25214A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379955 | ||||||
chr1:218379960
|
G | A | 3 | a0001c0001t0012g0008a0001c0001t0012g0013a0001c0001t0012g0017 | 3 | HG02523.hp2 NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.347-25209G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379960 | ||||||
chr1:218379965
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.347-25204G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379965 | ||||||
chr1:218380187
|
C | T | 37 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(34): Show | 38 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.347-24982C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380187 | ||||||
chr1:218380201
|
C | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160 | 3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-24968C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380201 | ||||||
chr1:218380222
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.347-24947G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380222 | ||||||
chr1:218380404
|
T | G | 1 | a0001c0001t0067g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.347-24765T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380404 | ||||||
chr1:218380526
|
T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-24643T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380526 | ||||||
chr1:218380717
|
G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-24452G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380717 | ||||||
chr1:218380798
|
G | A | 1 | a0001c0001t0006g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.347-24371G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380798 | ||||||
chr1:218380884
|
C | T | 32 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0001g0087others(29): Show | 33 | HG01109.hp1 HG01169.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.347-24285C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380884 | ||||||
chr1:218381075
|
T | G | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-24094T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381075 | ||||||
chr1:218381091
|
C | G | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-24078C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381091 | ||||||
chr1:218381149
|
C | T | 2 | a0001c0001t0014g0174a0001c0001t0014g0191 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.347-24020C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381149 | ||||||
chr1:218381252
|
G | T | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-23917G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381252 | ||||||
chr1:218381258
|
G | GT | 114 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0093others(111): Show | 115 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.347-23896dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381258 | |||||
chr1:218381258
|
G | GTT | 11 | a0001c0001t0002g0179a0001c0001t0003g0217a0001c0001t0003g0227others(8): Show | 11 | HG01109.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-23897_347-2389 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381258 | |||||
chr1:218381258
|
G | T | 2 | a0001c0001t0002g0127a0001c0001t0027g0269 | 2 | HG02615.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.347-23911G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381258 | ||||||
chr1:218381263
|
T | TG | 2 | a0001c0001t0001g0001a0001c0001t0003g0045 | 3 | HG02056.hp2 NA18974.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.347-23906_347-2390 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381263 | ||||||
chr1:218381282
|
G | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-23887G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381282 | ||||||
chr1:218381290
|
CTG | C | 5 | a0001c0001t0019g0272a0001c0001t0026g0278a0001c0001t0028g0275others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-23877_347-2387 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381290 | |||||
chr1:218381444
|
C | T | 15 | a0001c0001t0002g0091a0001c0001t0002g0121a0001c0001t0010g0018others(12): Show | 15 | HG02056.hp1 HG02165.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-23725C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381444 | ||||||
chr1:218381490
|
G | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0097others(75): Show | 80 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.347-23679G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381490 | ||||||
chr1:218381501
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-23668G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381501 | ||||||
chr1:218381832
|
G | GGT | 11 | a0001c0001t0003g0253a0001c0001t0005g0111a0001c0001t0005g0164others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-23321_347-2332 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381832 | |||||
chr1:218381832
|
G | T | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-23337G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381832 | ||||||
chr1:218381832
|
GGT | G | 4 | a0001c0001t0001g0085a0001c0001t0001g0096a0001c0001t0076g0281others(1): Show | 4 | HG00738.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-23321_347-2332 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381832 | |||||
chr1:218381851
|
A | T | 3 | a0001c0001t0001g0103a0001c0001t0052g0055a0001c0001t0067g0120 | 3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-23318A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381851 | ||||||
chr1:218381859
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160 | 3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-23310G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381859 | ||||||
chr1:218381992
|
T | C | 1 | a0001c0001t0010g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.347-23177T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381992 | ||||||
chr1:218382009
|
G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-23160G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382009 | ||||||
chr1:218382013
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-23156C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382013 | ||||||
chr1:218382175
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0253others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-22994C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382175 | ||||||
chr1:218382250
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-22919C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382250 | ||||||
chr1:218382358
|
G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-22811G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382358 | ||||||
chr1:218382694
|
T | C | 38 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0093others(35): Show | 38 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.347-22475T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382694 | ||||||
chr1:218382752
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0159a0001c0001t0001g0161others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-22417G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382752 | ||||||
chr1:218382860
|
C | T | 107 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0081others(104): Show | 108 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.347-22309C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382860 | ||||||
chr1:218382863
|
G | A | 1 | a0001c0001t0036g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.347-22306G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382863 | ||||||
chr1:218382955
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(105): Show | 111 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.347-22214T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382955 | ||||||
chr1:218382980
|
G | T | 1 | a0001c0001t0043g0052 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.347-22189G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382980 | ||||||
chr1:218383349
|
C | A | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-21820C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383349 | ||||||
chr1:218383377
|
CT | C | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-21787delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218383377 | |||||
chr1:218383492
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-21677C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383492 | ||||||
chr1:218383532
|
G | T | 1 | a0001c0001t0003g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.347-21637G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383532 | ||||||
chr1:218383658
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160 | 3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-21511C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383658 | ||||||
chr1:218383703
|
C | T | 4 | a0001c0001t0004g0252a0001c0001t0018g0277a0001c0001t0026g0279others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-21466C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383703 | ||||||
chr1:218383937
|
G | T | 13 | a0001c0001t0002g0091a0001c0001t0010g0018a0001c0001t0010g0019others(10): Show | 13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-21232G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383937 | ||||||
chr1:218383968
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0075g0065 | 2 | HG01256.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.347-21201G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383968 | ||||||
chr1:218383988
|
T | G | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-21181T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383988 | ||||||
chr1:218384123
|
GA | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(154): Show | 161 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.347-21035delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218384123 | |||||
chr1:218384175
|
G | A | 11 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0161others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-20994G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384175 | ||||||
chr1:218384267
|
T | C | 33 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0106others(30): Show | 33 | HG00438.hp1 HG00738.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-20902T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384267 | ||||||
chr1:218384313
|
C | T | 13 | a0001c0001t0002g0091a0001c0001t0010g0018a0001c0001t0010g0019others(10): Show | 13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-20856C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384313 | ||||||
chr1:218384314
|
G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-20855G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384314 | ||||||
chr1:218384320
|
AGG | A | 5 | a0001c0001t0004g0224a0001c0001t0009g0222a0001c0001t0011g0225others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-20848_347-2084 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384320 | ||||||
chr1:218384401
|
A | G | 2 | a0001c0001t0004g0040a0001c0001t0004g0243 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.347-20768A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384401 | ||||||
chr1:218384419
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0075g0065 | 2 | HG01256.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.347-20750T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384419 | ||||||
chr1:218384470
|
G | A | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-20699G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384470 | ||||||
chr1:218384565
|
C | T | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-20604C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384565 | ||||||
chr1:218384578
|
G | T | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-20591G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384578 | ||||||
chr1:218384644
|
T | C | 3 | a0001c0001t0004g0252a0001c0001t0026g0279a0001c0001t0081g0268 | 3 | HG01243.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-20525T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384644 | ||||||
chr1:218384737
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0002g0095 | 2 | HG00621.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.347-20432T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384737 | ||||||
chr1:218384843
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.347-20326G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384843 | ||||||
chr1:218384985
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(99): Show | 105 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-20184C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384985 | ||||||
chr1:218385036
|
C | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.347-20133C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385036 | ||||||
chr1:218385097
|
G | A | 1 | a0001c0001t0005g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347-20072G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385097 | ||||||
chr1:218385103
|
A | G | 33 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0106others(30): Show | 33 | HG00438.hp1 HG00738.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-20066A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385103 | ||||||
chr1:218385113
|
CCT | C | 7 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(4): Show | 7 | HG01169.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-20051_347-2005 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218385113 | |||||
chr1:218385116
|
C | T | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-20053C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385116 | ||||||
chr1:218385189
|
A | C | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-19980A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385189 | ||||||
chr1:218385246
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(150): Show | 156 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.347-19923G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385246 | ||||||
chr1:218385343
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.347-19826T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385343 | ||||||
chr1:218385369
|
C | T | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-19800C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385369 | ||||||
chr1:218385411
|
C | T | 3 | a0001c0001t0003g0025a0001c0001t0018g0277a0001c0001t0077g0280 | 3 | HG02258.hp1 HG03490.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.347-19758C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385411 | ||||||
chr1:218385553
|
C | A | 3 | a0001c0001t0004g0252a0001c0001t0026g0279a0001c0001t0081g0268 | 3 | HG01243.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-19616C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385553 | ||||||
chr1:218385634
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0052g0055a0001c0001t0067g0120 | 3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-19535T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385634 | ||||||
chr1:218385690
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(108): Show | 114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.347-19479G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385690 | ||||||
chr1:218385752
|
T | C | 1 | a0001c0001t0033g0044 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.347-19417T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385752 | ||||||
chr1:218385938
|
A | G | 58 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0106others(55): Show | 59 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-19231A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385938 | ||||||
chr1:218386017
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-19152G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386017 | ||||||
chr1:218386071
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0002g0137a0001c0001t0015g0135 | 3 | HG00558.hp1 NA18979.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.347-19098G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386071 | ||||||
chr1:218386133
|
C | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(109): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.347-19036C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386133 | ||||||
chr1:218386198
|
G | C | 3 | a0001c0001t0001g0103a0001c0001t0052g0055a0001c0001t0067g0120 | 3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-18971G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386198 | ||||||
chr1:218386269
|
G | A | 13 | a0001c0001t0002g0091a0001c0001t0010g0018a0001c0001t0010g0019others(10): Show | 13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-18900G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386269 | ||||||
chr1:218386533
|
T | C | 8 | a0001c0001t0004g0224a0001c0001t0005g0111a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-18636T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386533 | ||||||
chr1:218386567
|
T | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0116a0001c0001t0026g0278others(3): Show | 6 | HG01256.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-18602T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386567 | ||||||
chr1:218386664
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0031g0284 | 3 | HG01433.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.347-18505G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386664 | ||||||
chr1:218386823
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(107): Show | 113 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.347-18346C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386823 | ||||||
chr1:218386888
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0116a0001c0001t0026g0278others(3): Show | 6 | HG01256.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-18281G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386888 | ||||||
chr1:218386998
|
C | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347-18171C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386998 | ||||||
chr1:218387115
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.347-18054G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387115 | ||||||
chr1:218387311
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(4): Show | 7 | HG01169.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-17858A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387311 | ||||||
chr1:218387347
|
A | C | 1 | a0001c0001t0068g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.347-17822A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387347 | ||||||
chr1:218387398
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.347-17771G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387398 | ||||||
chr1:218387598
|
G | T | 1 | a0001c0001t0074g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.347-17571G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387598 | ||||||
chr1:218387620
|
G | GA | 9 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0227others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-17548dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218387620 | |||||
chr1:218387630
|
G | C | 3 | a0001c0001t0001g0103a0001c0001t0026g0278a0001c0001t0084g0286 | 3 | HG02486.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347-17539G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387630 | ||||||
chr1:218387690
|
T | C | 1 | a0001c0001t0004g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.347-17479T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387690 | ||||||
chr1:218387834
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0005g0160others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-17335A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387834 | ||||||
chr1:218387944
|
C | G | 6 | a0001c0001t0003g0253a0001c0001t0004g0252a0001c0001t0018g0274others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-17225C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387944 | ||||||
chr1:218387959
|
C | T | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-17210C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387959 | ||||||
chr1:218388075
|
T | G | 1 | a0002c0003t0002g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.347-17094T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388075 | ||||||
chr1:218388102
|
A | C | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-17067A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388102 | ||||||
chr1:218388239
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0077others(122): Show | 126 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.347-16930C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388239 | ||||||
chr1:218388327
|
GC | G | 18 | a0001c0001t0001g0143a0001c0001t0002g0112a0001c0001t0002g0195others(15): Show | 18 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.347-16835delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218388327 | |||||
chr1:218388330
|
C | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347-16839C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388330 | ||||||
chr1:218388432
|
GACA | G | 13 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0103others(10): Show | 13 | HG01169.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-16733_347-1673 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218388432 | |||||
chr1:218388446
|
G | A | 1 | a0001c0001t0029g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.347-16723G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388446 | ||||||
chr1:218388631
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.347-16538G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388631 | ||||||
chr1:218388638
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347-16531G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388638 | ||||||
chr1:218389011
|
C | T | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347-16158C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389011 | ||||||
chr1:218389179
|
T | C | 1 | a0001c0001t0007g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.347-15990T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389179 | ||||||
chr1:218389199
|
C | A | 21 | a0001c0001t0001g0087a0001c0001t0001g0103a0001c0001t0004g0223others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-15970C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389199 | ||||||
chr1:218389297
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347-15872G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389297 | ||||||
chr1:218389366
|
C | T | 27 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(24): Show | 27 | HG01261.hp1 HG01346.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.347-15803C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389366 | ||||||
chr1:218389497
|
T | A | 5 | a0001c0001t0005g0111a0001c0001t0005g0160a0001c0001t0014g0174others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-15672T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389497 | ||||||
chr1:218389526
|
C | T | 32 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(29): Show | 32 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.347-15643C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389526 | ||||||
chr1:218389581
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0002g0204a0001c0001t0029g0266 | 3 | HG02622.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.347-15588A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389581 | ||||||
chr1:218389694
|
C | T | 76 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0103others(73): Show | 76 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(73): Show |
intron_variant | MODIFIER | c.347-15475C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389694 | ||||||
chr1:218389884
|
C | G | 1 | a0001c0001t0057g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.347-15285C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389884 | ||||||
chr1:218389973
|
A | C | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-15196A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389973 | ||||||
chr1:218390335
|
C | T | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-14834C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390335 | ||||||
chr1:218390350
|
AC | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0129a0001c0001t0004g0047 | 3 | NA18974.hp2 NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.347-14818delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390350 | ||||||
chr1:218390351
|
C | A | 78 | a0001c0001t0002g0057a0001c0001t0002g0092a0001c0001t0002g0095others(75): Show | 80 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.347-14818C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390351 | ||||||
chr1:218390467
|
T | C | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-14702T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390467 | ||||||
chr1:218390486
|
G | A | 1 | a0001c0001t0015g0135 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.347-14683G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390486 | ||||||
chr1:218390791
|
C | A | 1 | a0001c0001t0062g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-14378C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390791 | ||||||
chr1:218391010
|
T | C | 3 | a0001c0001t0003g0227a0001c0001t0028g0275a0001c0001t0028g0276 | 3 | HG01109.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-14159T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391010 | ||||||
chr1:218391155
|
G | A | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-14014G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391155 | ||||||
chr1:218391302
|
C | T | 70 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(67): Show | 70 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.347-13867C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391302 | ||||||
chr1:218391340
|
C | T | 1 | a0001c0001t0037g0215 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.347-13829C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391340 | ||||||
chr1:218391431
|
G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-13738G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391431 | ||||||
chr1:218391521
|
C | T | 1 | a0001c0001t0015g0200 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.347-13648C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391521 | ||||||
chr1:218391539
|
C | T | 147 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(144): Show | 149 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.347-13630C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391539 | ||||||
chr1:218391553
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347-13616C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391553 | ||||||
chr1:218391628
|
C | G | 133 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(130): Show | 133 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(130): Show |
intron_variant | MODIFIER | c.347-13541C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391628 | ||||||
chr1:218391635
|
T | C | 70 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(67): Show | 70 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.347-13534T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391635 | ||||||
chr1:218391641
|
A | C | 1 | a0001c0001t0039g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-13528A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391641 | ||||||
chr1:218391959
|
G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-13210G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391959 | ||||||
chr1:218391982
|
G | A | 138 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(135): Show | 140 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.347-13187G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391982 | ||||||
chr1:218392070
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-13099G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392070 | ||||||
chr1:218392080
|
G | A | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-13089G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392080 | ||||||
chr1:218392103
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.347-13066G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392103 | ||||||
chr1:218392168
|
G | A | 21 | a0001c0001t0001g0087a0001c0001t0003g0255a0001c0001t0004g0223others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.347-13001G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392168 | ||||||
chr1:218392301
|
C | T | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-12868C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392301 | ||||||
chr1:218392364
|
A | T | 1 | a0001c0001t0004g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.347-12805A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392364 | ||||||
chr1:218392595
|
C | CTGTCT | 10 | a0001c0001t0002g0091a0001c0001t0002g0173a0001c0001t0004g0031others(7): Show | 10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-12560_347-1255 others(9): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218392595 | |||||
chr1:218392805
|
C | A | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-12364C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392805 | ||||||
chr1:218392823
|
T | G | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-12346T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392823 | ||||||
chr1:218392900
|
G | A | 1 | a0001c0001t0011g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-12269G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392900 | ||||||
chr1:218392908
|
T | C | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-12261T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392908 | ||||||
chr1:218393206
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-11963C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393206 | ||||||
chr1:218393269
|
A | G | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-11900A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393269 | ||||||
chr1:218393297
|
A | G | 2 | a0001c0001t0005g0203a0001c0001t0087g0210 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.347-11872A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393297 | ||||||
chr1:218393513
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.347-11656A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393513 | ||||||
chr1:218393536
|
T | G | 45 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(42): Show | 45 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.347-11633T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393536 | ||||||
chr1:218393598
|
C | G | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-11571C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393598 | ||||||
chr1:218393767
|
C | G | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-11402C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393767 | ||||||
chr1:218393999
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-11170C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393999 | ||||||
chr1:218394100
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0105others(3): Show | 6 | HG00738.hp1 HG02004.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-11069G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394100 | ||||||
chr1:218394152
|
G | A | 150 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(147): Show | 152 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.347-11017G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394152 | ||||||
chr1:218394209
|
G | A | 3 | a0001c0001t0004g0252a0001c0001t0075g0065a0001c0001t0081g0268 | 3 | HG02615.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-10960G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394209 | ||||||
chr1:218394289
|
C | T | 13 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-10880C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394289 | ||||||
chr1:218394306
|
A | T | 10 | a0001c0001t0002g0091a0001c0001t0002g0173a0001c0001t0004g0031others(7): Show | 10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-10863A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394306 | ||||||
chr1:218394634
|
G | A | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.347-10535G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394634 | ||||||
chr1:218395017
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0140others(19): Show | 23 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.347-10152G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395017 | ||||||
chr1:218395131
|
G | A | 67 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(64): Show | 67 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-10038G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395131 | ||||||
chr1:218395140
|
T | A | 69 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(66): Show | 69 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.347-10029T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395140 | ||||||
chr1:218395197
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0181 | 2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.347-9972G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395197 | ||||||
chr1:218395428
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.347-9741C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395428 | ||||||
chr1:218395462
|
G | A | 67 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(64): Show | 67 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-9707G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395462 | ||||||
chr1:218395487
|
A | G | 134 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(131): Show | 134 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(131): Show |
intron_variant | MODIFIER | c.347-9682A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395487 | ||||||
chr1:218395564
|
A | G | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-9605A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395564 | ||||||
chr1:218395611
|
C | CT | 55 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0085others(52): Show | 55 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.347-9543dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218395611 | |||||
chr1:218395611
|
CT | C | 20 | a0001c0001t0001g0087a0001c0001t0003g0255a0001c0001t0004g0223others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.347-9543delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218395611 | |||||
chr1:218395618
|
T | C | 1 | a0001c0001t0004g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.347-9551T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395618 | ||||||
chr1:218395646
|
C | T | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.347-9523C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395646 | ||||||
chr1:218395685
|
C | A | 49 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0085others(46): Show | 49 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.347-9484C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395685 | ||||||
chr1:218395772
|
T | C | 67 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(64): Show | 67 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-9397T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395772 | ||||||
chr1:218395816
|
A | G | 2 | a0001c0001t0006g0089a0001c0001t0006g0145 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.347-9353A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395816 | ||||||
chr1:218395836
|
G | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-9333G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395836 | ||||||
chr1:218395866
|
G | A | 67 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(64): Show | 67 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-9303G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395866 | ||||||
chr1:218395883
|
G | A | 1 | a0001c0001t0035g0254 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.347-9286G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395883 | ||||||
chr1:218395905
|
C | T | 30 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0096others(27): Show | 30 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.347-9264C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395905 | ||||||
chr1:218395999
|
A | G | 1 | a0001c0001t0007g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.347-9170A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395999 | ||||||
chr1:218396128
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-9041C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396128 | ||||||
chr1:218396151
|
C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-9018C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396151 | ||||||
chr1:218396308
|
GTGGAATT others(9): Show |
G | 1 | a0001c0001t0024g0005 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.347-8860_347-8845d others(18): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396308 | ||||||
chr1:218396349
|
G | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-8820G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396349 | ||||||
chr1:218396541
|
CTT | C | 13 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-8617_347-8616d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218396541 | |||||
chr1:218396762
|
C | G | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.347-8407C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396762 | ||||||
chr1:218396834
|
C | T | 28 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(25): Show | 28 | HG01261.hp1 HG01346.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-8335C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396834 | ||||||
chr1:218396989
|
C | T | 46 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(43): Show | 46 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(43): Show |
intron_variant | MODIFIER | c.347-8180C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396989 | ||||||
chr1:218397128
|
C | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0103a0001c0001t0001g0158others(2): Show | 5 | HG01891.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-8041C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397128 | ||||||
chr1:218397161
|
A | C | 1 | a0001c0001t0004g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.347-8008A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397161 | ||||||
chr1:218397185
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-7984G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397185 | ||||||
chr1:218397266
|
T | TA | 13 | a0001c0001t0001g0128a0001c0001t0002g0091a0001c0001t0002g0173others(10): Show | 13 | HG02056.hp1 HG02074.hp1 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-7888dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | |||||
chr1:218397266
|
T | TAA | 44 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(41): Show | 44 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.347-7889_347-7888d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | |||||
chr1:218397266
|
TA | T | 21 | a0001c0001t0001g0087a0001c0001t0003g0255a0001c0001t0004g0223others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.347-7888delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | |||||
chr1:218397290
|
G | A | 13 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-7879G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397290 | ||||||
chr1:218397301
|
T | G | 73 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(70): Show | 74 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.347-7868T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397301 | ||||||
chr1:218397421
|
G | C | 6 | a0001c0001t0005g0111a0001c0001t0005g0160a0001c0001t0014g0174others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-7748G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397421 | ||||||
chr1:218397561
|
C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-7608C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397561 | ||||||
chr1:218397563
|
C | CA | 9 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0002g0115others(6): Show | 9 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-7587dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | |||||
chr1:218397563
|
C | CAA | 53 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(50): Show | 53 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.347-7588_347-7587d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | |||||
chr1:218397563
|
CA | C | 87 | a0001c0001t0001g0061a0001c0001t0001g0103a0001c0001t0001g0158others(84): Show | 88 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.347-7587delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | |||||
chr1:218397583
|
G | A | 8 | a0001c0001t0004g0224a0001c0001t0004g0252a0001c0001t0011g0225others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-7586G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397583 | ||||||
chr1:218397645
|
T | C | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-7524T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397645 | ||||||
chr1:218397724
|
A | G | 69 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(66): Show | 69 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.347-7445A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397724 | ||||||
chr1:218397738
|
T | C | 1 | a0001c0001t0053g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.347-7431T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397738 | ||||||
chr1:218397903
|
G | A | 1 | a0001c0001t0051g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-7266G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397903 | ||||||
chr1:218397972
|
C | G | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-7197C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397972 | ||||||
chr1:218398051
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-7118A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398051 | ||||||
chr1:218398219
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-6950G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398219 | ||||||
chr1:218398249
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.347-6920G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398249 | ||||||
chr1:218398415
|
A | T | 80 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0092others(77): Show | 82 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.347-6754A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398415 | ||||||
chr1:218398572
|
T | A | 1 | a0001c0001t0080g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347-6597T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398572 | ||||||
chr1:218398662
|
G | A | 80 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0092others(77): Show | 82 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.347-6507G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398662 | ||||||
chr1:218398680
|
C | T | 3 | a0001c0001t0050g0205a0001c0001t0057g0141a0001c0001t0063g0086 | 3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.347-6489C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398680 | ||||||
chr1:218398683
|
G | A | 1 | a0001c0001t0009g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.347-6486G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398683 | ||||||
chr1:218398733
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-6436G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398733 | ||||||
chr1:218398760
|
G | T | 10 | a0001c0001t0002g0091a0001c0001t0002g0173a0001c0001t0004g0031others(7): Show | 10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-6409G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398760 | ||||||
chr1:218398776
|
C | T | 1 | a0001c0001t0017g0146 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.347-6393C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398776 | ||||||
chr1:218398895
|
T | G | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-6274T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398895 | ||||||
chr1:218398925
|
C | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-6244C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398925 | ||||||
chr1:218399009
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-6160A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399009 | ||||||
chr1:218399044
|
C | T | 1 | a0001c0001t0039g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-6125C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399044 | ||||||
chr1:218399131
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.347-6038C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399131 | ||||||
chr1:218399238
|
C | G | 26 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0102others(23): Show | 26 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-5931C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399238 | ||||||
chr1:218399257
|
C | T | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-5912C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399257 | ||||||
chr1:218399288
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347-5881G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399288 | ||||||
chr1:218399353
|
G | A | 19 | a0001c0001t0001g0087a0001c0001t0003g0255a0001c0001t0004g0223others(16): Show | 19 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.347-5816G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399353 | ||||||
chr1:218399426
|
T | G | 65 | a0001c0001t0001g0087a0001c0001t0003g0253a0001c0001t0003g0255others(62): Show | 65 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.347-5743T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399426 | ||||||
chr1:218399466
|
A | G | 68 | a0001c0001t0001g0087a0001c0001t0003g0227a0001c0001t0003g0253others(65): Show | 68 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.347-5703A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399466 | ||||||
chr1:218399708
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-5461A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399708 | ||||||
chr1:218399764
|
T | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-5405T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399764 | ||||||
chr1:218399907
|
G | A | 12 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-5262G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399907 | ||||||
chr1:218400323
|
G | A | 3 | a0001c0001t0011g0226a0001c0001t0020g0004a0001c0001t0067g0120 | 4 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-4846G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400323 | ||||||
chr1:218400358
|
C | G | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-4811C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400358 | ||||||
chr1:218400399
|
T | C | 176 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0087others(173): Show | 178 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(175): Show |
intron_variant | MODIFIER | c.347-4770T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400399 | ||||||
chr1:218400426
|
C | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-4743C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400426 | ||||||
chr1:218400800
|
CCTGACCC others(3): Show |
C | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-4365_347-4356d others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218400800 | |||||
chr1:218400816
|
A | G | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-4353A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400816 | ||||||
chr1:218400824
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.347-4345G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400824 | ||||||
chr1:218400870
|
T | C | 2 | a0001c0001t0005g0164a0001c0001t0018g0277 | 2 | HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.347-4299T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400870 | ||||||
chr1:218401090
|
C | T | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-4079C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401090 | ||||||
chr1:218401100
|
G | C | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-4069G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401100 | ||||||
chr1:218401133
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.347-4036G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401133 | ||||||
chr1:218401228
|
A | G | 1 | a0001c0001t0063g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.347-3941A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401228 | ||||||
chr1:218401242
|
A | AT | 43 | a0001c0001t0003g0253a0001c0001t0004g0209a0001c0001t0005g0078others(40): Show | 43 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.347-3926dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218401242 | |||||
chr1:218401447
|
C | T | 73 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(70): Show | 73 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.347-3722C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401447 | ||||||
chr1:218401465
|
G | A | 5 | a0001c0001t0005g0111a0001c0001t0014g0174a0001c0001t0014g0191others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3704G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401465 | ||||||
chr1:218401530
|
G | A | 1 | a0001c0001t0052g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.347-3639G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401530 | ||||||
chr1:218401576
|
G | A | 10 | a0001c0001t0002g0091a0001c0001t0002g0173a0001c0001t0004g0031others(7): Show | 10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-3593G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401576 | ||||||
chr1:218401685
|
C | T | 12 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3484C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401685 | ||||||
chr1:218401828
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0003g0218a0001c0001t0003g0219others(2): Show | 5 | HG01169.hp1 HG02486.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3341G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401828 | ||||||
chr1:218401829
|
C | T | 1 | a0001c0001t0009g0250 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.347-3340C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401829 | ||||||
chr1:218401834
|
C | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0115a0001c0001t0004g0003others(1): Show | 5 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-3335C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401834 | ||||||
chr1:218401860
|
G | A | 93 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(90): Show | 95 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.347-3309G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401860 | ||||||
chr1:218401996
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.347-3173G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401996 | ||||||
chr1:218401998
|
G | A | 12 | a0001c0001t0001g0087a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3171G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401998 | ||||||
chr1:218402051
|
G | A | 1 | a0001c0001t0050g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347-3118G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402051 | ||||||
chr1:218402130
|
A | G | 227 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(224): Show | 229 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.347-3039A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402130 | ||||||
chr1:218402285
|
A | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-2884A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402285 | ||||||
chr1:218402380
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.347-2789A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402380 | ||||||
chr1:218402544
|
GA | G | 10 | a0001c0001t0001g0085a0001c0001t0021g0221a0001c0001t0021g0228others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-2618delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218402544 | |||||
chr1:218402545
|
A | G | 103 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0002g0056others(100): Show | 104 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.347-2624A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402545 | ||||||
chr1:218402683
|
T | C | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-2486T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402683 | ||||||
chr1:218402853
|
C | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.347-2316C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402853 | ||||||
chr1:218402862
|
G | A | 3 | a0001c0001t0003g0022a0001c0001t0027g0270a0001c0001t0031g0284 | 3 | HG02717.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.347-2307G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402862 | ||||||
chr1:218402935
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-2234C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402935 | ||||||
chr1:218402987
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.347-2182C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402987 | ||||||
chr1:218403203
|
T | G | 2 | a0001c0001t0001g0140a0001c0001t0051g0168 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.347-1966T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403203 | ||||||
chr1:218403207
|
GT | G | 58 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0209others(55): Show | 58 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.347-1955delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218403207 | |||||
chr1:218403328
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0084g0286 | 2 | HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347-1841G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403328 | ||||||
chr1:218403782
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0256 | 3 | HG02109.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.347-1387G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403782 | ||||||
chr1:218403836
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.347-1333G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403836 | ||||||
chr1:218403953
|
G | C | 51 | a0001c0001t0003g0253a0001c0001t0004g0209a0001c0001t0005g0078others(48): Show | 51 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(48): Show |
intron_variant | MODIFIER | c.347-1216G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403953 | ||||||
chr1:218403984
|
G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-1185G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403984 | ||||||
chr1:218404051
|
C | CA | 45 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0209others(42): Show | 45 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.347-1098dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | |||||
chr1:218404051
|
C | CAA | 10 | a0001c0001t0005g0111a0001c0001t0005g0164a0001c0001t0005g0203others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-1099_347-1098d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | |||||
chr1:218404051
|
CA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(203): Show | 208 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.347-1098delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | |||||
chr1:218404051
|
CAA | C | 7 | a0001c0001t0001g0076a0001c0001t0011g0226a0001c0001t0011g0260others(4): Show | 8 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-1099_347-1098d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | |||||
chr1:218404101
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.347-1068C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218404101 | ||||||
chr1:218404236
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-933C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218404236 | ||||||
chr1:218405343
|
T | TTTGTTG | 39 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(36): Show | 39 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.510+38_510+43dupGT others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | |||||
chr1:218405343
|
T | TTTGTTGT others(2): Show |
6 | a0001c0001t0003g0253a0001c0001t0005g0160a0001c0001t0019g0283others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+35_510+43dupGT others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | |||||
chr1:218405343
|
T | TTTGTTGT others(5): Show |
2 | a0001c0001t0004g0209a0001c0001t0018g0277 | 2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.510+32_510+43dupGT others(10): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | |||||
chr1:218405343
|
TTTG | T | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+41_510+43delGT others(1): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | |||||
chr1:218405384
|
A | ACT | 3 | a0001c0001t0003g0022a0001c0001t0027g0270a0001c0001t0031g0284 | 3 | HG02717.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.510+69_510+70dupCT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405384 | |||||
chr1:218405422
|
T | G | 1 | a0001c0001t0002g0125 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.510+90T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218405422 | ||||||
chr1:218405872
|
G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.510+540G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218405872 | ||||||
chr1:218406167
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.510+835C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406167 | ||||||
chr1:218406178
|
G | A | 10 | a0001c0001t0005g0111a0001c0001t0014g0174a0001c0001t0014g0191others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+846G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406178 | ||||||
chr1:218406192
|
T | TAC | 110 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0087others(107): Show | 111 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.510+883_510+884dup others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | |||||
chr1:218406192
|
T | TACAC | 50 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0236others(47): Show | 50 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+881_510+884dup others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | |||||
chr1:218406192
|
T | TACACAC | 3 | a0001c0001t0004g0209a0001c0001t0026g0278a0001c0001t0053g0058 | 3 | HG02486.hp1 HG02922.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.510+879_510+884dup others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | |||||
chr1:218406192
|
TAC | T | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+883_510+884del others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | |||||
chr1:218406212
|
C | G | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510+880C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406212 | ||||||
chr1:218406302
|
G | A | 58 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0209others(55): Show | 58 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.510+970G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406302 | ||||||
chr1:218406338
|
A | AT | 58 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0209others(55): Show | 58 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.510+1010dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406338 | |||||
chr1:218406409
|
G | A | 53 | a0001c0001t0003g0253a0001c0001t0003g0255a0001c0001t0004g0209others(50): Show | 53 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(50): Show |
intron_variant | MODIFIER | c.510+1077G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406409 | ||||||
chr1:218406511
|
A | G | 45 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(42): Show | 45 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+1179A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406511 | ||||||
chr1:218406526
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.510+1194C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406526 | ||||||
chr1:218406643
|
A | G | 163 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0194others(160): Show | 164 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.510+1311A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406643 | ||||||
chr1:218406658
|
G | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+1326G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406658 | ||||||
chr1:218406823
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510+1491G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406823 | ||||||
chr1:218406850
|
C | A | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.510+1518C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406850 | ||||||
chr1:218406883
|
G | A | 4 | a0001c0001t0007g0119a0001c0001t0007g0123a0001c0001t0007g0130others(1): Show | 4 | HG01496.hp2 HG01928.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1551G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406883 | ||||||
chr1:218407028
|
A | G | 218 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(215): Show | 219 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.510+1696A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407028 | ||||||
chr1:218407117
|
A | T | 47 | a0001c0001t0003g0255a0001c0001t0005g0078a0001c0001t0005g0079others(44): Show | 47 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+1785A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407117 | ||||||
chr1:218407141
|
A | C | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.510+1809A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407141 | ||||||
chr1:218407159
|
G | T | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+1827G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407159 | ||||||
chr1:218407174
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0003g0240a0001c0001t0048g0241 | 3 | HG00741.hp2 HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.510+1842T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407174 | ||||||
chr1:218407426
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+2094C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407426 | ||||||
chr1:218407467
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+2135C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407467 | ||||||
chr1:218407709
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0035g0254a0001c0001t0076g0281others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+2377G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407709 | ||||||
chr1:218407755
|
A | G | 6 | a0001c0001t0005g0111a0001c0001t0005g0160a0001c0001t0014g0174others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+2423A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407755 | ||||||
chr1:218407760
|
G | T | 48 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(45): Show | 48 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+2428G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407760 | ||||||
chr1:218408088
|
A | T | 7 | a0001c0001t0003g0253a0001c0001t0018g0277a0001c0001t0035g0254others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+2756A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408088 | ||||||
chr1:218408105
|
T | G | 52 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(49): Show | 52 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+2773T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408105 | ||||||
chr1:218408167
|
T | C | 166 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(163): Show | 167 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.510+2835T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408167 | ||||||
chr1:218408180
|
C | T | 6 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+2848C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408180 | ||||||
chr1:218408221
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510+2889G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408221 | ||||||
chr1:218408253
|
A | G | 40 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(37): Show | 40 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+2921A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408253 | ||||||
chr1:218408275
|
T | C | 92 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(89): Show | 92 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.510+2943T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408275 | ||||||
chr1:218408349
|
C | T | 2 | a0001c0001t0028g0275a0001c0001t0028g0276 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+3017C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408349 | ||||||
chr1:218408516
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+3184A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408516 | ||||||
chr1:218409021
|
C | T | 5 | a0001c0001t0002g0156a0001c0001t0002g0198a0001c0001t0004g0026others(2): Show | 5 | NA18940.hp2 NA18993.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+3689C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409021 | ||||||
chr1:218409089
|
G | A | 3 | a0001c0001t0035g0254a0001c0001t0076g0281a0001c0001t0086g0213 | 3 | HG02717.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510+3757G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409089 | ||||||
chr1:218409202
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+3870C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409202 | ||||||
chr1:218409273
|
C | A | 1 | a0001c0001t0064g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510+3941C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409273 | ||||||
chr1:218409294
|
A | G | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510+3962A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409294 | ||||||
chr1:218409301
|
A | G | 1 | a0001c0001t0004g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.510+3969A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409301 | ||||||
chr1:218409436
|
T | C | 99 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0002g0056others(96): Show | 100 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.510+4104T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409436 | ||||||
chr1:218409447
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0003g0049 | 2 | NA19074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.510+4115G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409447 | ||||||
chr1:218409499
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510+4167T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409499 | ||||||
chr1:218409598
|
A | G | 5 | a0001c0001t0002g0204a0001c0001t0013g0211a0001c0001t0013g0212others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+4266A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409598 | ||||||
chr1:218409618
|
T | C | 1 | a0001c0001t0053g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.510+4286T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409618 | ||||||
chr1:218409665
|
GA | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(51): Show | 54 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.510+4343delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218409665 | |||||
chr1:218409675
|
A | C | 11 | a0001c0001t0005g0111a0001c0001t0005g0160a0001c0001t0014g0174others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+4343A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409675 | ||||||
chr1:218409889
|
A | G | 3 | a0001c0001t0004g0209a0001c0001t0019g0283a0001c0001t0027g0269 | 3 | HG02559.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+4557A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409889 | ||||||
chr1:218410075
|
C | T | 2 | a0001c0001t0003g0253a0001c0001t0018g0277 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.510+4743C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410075 | ||||||
chr1:218410156
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.510+4824C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410156 | ||||||
chr1:218410428
|
C | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5096C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410428 | ||||||
chr1:218410485
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5153C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410485 | ||||||
chr1:218410958
|
A | G | 6 | a0001c0001t0002g0173a0001c0001t0010g0020a0001c0001t0030g0009others(3): Show | 6 | NA18986.hp2 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+5626A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410958 | ||||||
chr1:218410972
|
G | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5640G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410972 | ||||||
chr1:218410979
|
T | C | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5647T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410979 | ||||||
chr1:218411033
|
A | ATCC | 29 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0096others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.510+5703_510+5705d others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411033 | |||||
chr1:218411075
|
A | G | 1 | a0001c0001t0016g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.510+5743A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411075 | ||||||
chr1:218411077
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(51): Show | 54 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.510+5745C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411077 | ||||||
chr1:218411125
|
C | T | 1 | a0001c0001t0035g0254 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.510+5793C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411125 | ||||||
chr1:218411155
|
T | G | 6 | a0001c0001t0001g0103a0001c0001t0003g0255a0001c0001t0004g0209others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+5823T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411155 | ||||||
chr1:218411250
|
A | C | 1 | a0001c0001t0041g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510+5918A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411250 | ||||||
chr1:218411381
|
T | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+6049T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411381 | ||||||
chr1:218411610
|
A | C | 118 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(115): Show | 118 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(115): Show |
intron_variant | MODIFIER | c.510+6278A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411610 | ||||||
chr1:218411640
|
C | T | 1 | a0001c0001t0004g0040 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510+6308C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411640 | ||||||
chr1:218411789
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+6457C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411789 | ||||||
chr1:218411812
|
C | CAGAG | 44 | a0001c0001t0001g0103a0001c0001t0004g0209a0001c0001t0005g0078others(41): Show | 44 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+6482_510+6485d others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411812 | |||||
chr1:218411812
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+6480C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411812 | ||||||
chr1:218411845
|
A | T | 2 | a0001c0001t0018g0282a0001c0001t0029g0267 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510+6513A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411845 | ||||||
chr1:218411864
|
C | CA | 44 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0175others(41): Show | 44 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+6550dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | |||||
chr1:218411864
|
C | CAA | 8 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0036g0220others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+6549_510+6550d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | |||||
chr1:218411864
|
CA | C | 29 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0158others(26): Show | 30 | HG01109.hp1 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.510+6550delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | |||||
chr1:218411886
|
C | T | 1 | a0001c0001t0010g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510+6554C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411886 | ||||||
chr1:218411906
|
C | T | 40 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(37): Show | 40 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+6574C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411906 | ||||||
chr1:218412071
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510+6739C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412071 | ||||||
chr1:218412479
|
C | T | 93 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(90): Show | 93 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.510+7147C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412479 | ||||||
chr1:218412527
|
G | A | 5 | a0001c0001t0005g0111a0001c0001t0014g0174a0001c0001t0014g0191others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+7195G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412527 | ||||||
chr1:218412573
|
C | G | 9 | a0001c0001t0003g0022a0001c0001t0011g0226a0001c0001t0011g0260others(6): Show | 10 | HG01433.hp2 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+7241C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412573 | ||||||
chr1:218412599
|
C | T | 1 | a0001c0001t0004g0040 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510+7267C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412599 | ||||||
chr1:218412613
|
C | A | 1 | a0001c0001t0076g0281 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+7281C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412613 | ||||||
chr1:218412790
|
A | G | 226 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(223): Show | 228 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.510+7458A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412790 | ||||||
chr1:218412872
|
A | T | 94 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(91): Show | 94 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.510+7540A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412872 | ||||||
chr1:218412886
|
G | A | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+7554G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412886 | ||||||
chr1:218412955
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0004g0209a0001c0001t0019g0283others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+7623T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412955 | ||||||
chr1:218412956
|
T | C | 1 | a0001c0001t0067g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.510+7624T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412956 | ||||||
chr1:218412971
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0004g0209a0001c0001t0019g0283others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+7639T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412971 | ||||||
chr1:218412991
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.510+7659T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412991 | ||||||
chr1:218413180
|
T | C | 40 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(37): Show | 40 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+7848T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413180 | ||||||
chr1:218413363
|
G | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+8031G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413363 | ||||||
chr1:218413515
|
T | C | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8183T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413515 | ||||||
chr1:218413552
|
C | T | 1 | a0001c0001t0074g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.510+8220C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413552 | ||||||
chr1:218413769
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8437C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413769 | ||||||
chr1:218413824
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0004g0209a0001c0001t0019g0283others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+8492T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413824 | ||||||
chr1:218413940
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.510+8608G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413940 | ||||||
chr1:218414024
|
G | C | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8692G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414024 | ||||||
chr1:218414145
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.510+8813G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414145 | ||||||
chr1:218414195
|
A | T | 3 | a0001c0001t0050g0205a0001c0001t0057g0141a0001c0001t0063g0086 | 3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.510+8863A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414195 | ||||||
chr1:218414226
|
T | TGC | 3 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0256 | 3 | HG02109.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.510+8895_510+8896d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414226 | |||||
chr1:218414227
|
G | GCA | 34 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0093others(31): Show | 35 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.510+8921_510+8922d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | |||||
chr1:218414227
|
G | GCACACA | 3 | a0001c0001t0001g0114a0001c0001t0004g0209a0001c0001t0027g0269 | 3 | HG02615.hp2 HG02922.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.510+8917_510+8922d others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | |||||
chr1:218414227
|
GCA | G | 130 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(127): Show | 132 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.510+8921_510+8922d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | |||||
chr1:218414229
|
A | G | 46 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(43): Show | 46 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.510+8897A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414229 | ||||||
chr1:218414231
|
A | G | 29 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0096others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.510+8899A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414231 | ||||||
chr1:218414254
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+8922C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414254 | ||||||
chr1:218414294
|
A | G | 226 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(223): Show | 228 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.510+8962A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414294 | ||||||
chr1:218414685
|
A | C | 9 | a0001c0001t0001g0103a0001c0001t0003g0255a0001c0001t0004g0209others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+9353A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414685 | ||||||
chr1:218414796
|
CATGCAG | C | 93 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(90): Show | 93 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.510+9465_510+9470d others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414796 | ||||||
chr1:218414937
|
G | A | 108 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0002g0056others(105): Show | 110 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.510+9605G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414937 | ||||||
chr1:218415626
|
C | G | 7 | a0001c0001t0003g0253a0001c0001t0011g0208a0001c0001t0018g0277others(4): Show | 7 | HG01884.hp2 HG03471.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10294C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415626 | ||||||
chr1:218415673
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+10341C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415673 | ||||||
chr1:218415694
|
C | CA | 61 | a0001c0001t0001g0117a0001c0001t0001g0159a0001c0001t0002g0057others(58): Show | 62 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.510+10366dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | |||||
chr1:218415694
|
C | CAA | 40 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0002g0056others(37): Show | 40 | HG00621.hp1 HG01071.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+10365_510+1036 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | |||||
chr1:218415694
|
C | CAAA | 7 | a0001c0001t0001g0087a0001c0001t0002g0129a0001c0001t0002g0131others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10364_510+1036 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | |||||
chr1:218415697
|
AAG | A | 42 | a0001c0001t0001g0096a0001c0001t0005g0078a0001c0001t0005g0110others(39): Show | 42 | HG00738.hp1 HG01243.hp1 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.510+10367_510+1036 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415697 | |||||
chr1:218415698
|
AG | A | 39 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(36): Show | 39 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.510+10367delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415698 | ||||||
chr1:218415699
|
G | A | 145 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0102others(142): Show | 147 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.510+10367G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415699 | ||||||
chr1:218415722
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+10390A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415722 | ||||||
chr1:218415776
|
C | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+10444C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415776 | ||||||
chr1:218415855
|
T | C | 226 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(223): Show | 228 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.510+10523T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415855 | ||||||
chr1:218415860
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0010g0020a0001c0001t0033g0044 | 3 | NA18986.hp2 NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.510+10528A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415860 | ||||||
chr1:218416103
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0004g0209a0001c0001t0019g0283others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10771T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416103 | ||||||
chr1:218416124
|
TG | T | 42 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(39): Show | 42 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.510+10797delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218416124 | |||||
chr1:218416178
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0129 | 2 | NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.510+10846C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416178 | ||||||
chr1:218416292
|
C | CT | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+10970dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218416292 | |||||
chr1:218416296
|
T | C | 1 | a0001c0001t0067g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.510+10964T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416296 | ||||||
chr1:218416375
|
G | T | 3 | a0001c0001t0004g0209a0001c0001t0019g0283a0001c0001t0027g0269 | 3 | HG02559.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+11043G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416375 | ||||||
chr1:218416605
|
C | T | 2 | a0001c0001t0021g0221a0001c0001t0021g0228 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510+11273C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416605 | ||||||
chr1:218416649
|
C | T | 2 | a0001c0001t0021g0221a0001c0001t0021g0228 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510+11317C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416649 | ||||||
chr1:218416706
|
C | G | 1 | a0003c0004t0003g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.510+11374C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416706 | ||||||
chr1:218416813
|
A | G | 52 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0081others(49): Show | 52 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+11481A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416813 | ||||||
chr1:218416884
|
A | G | 10 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0003g0218others(7): Show | 10 | HG01169.hp1 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+11552A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416884 | ||||||
chr1:218417156
|
A | C | 7 | a0001c0001t0005g0111a0001c0001t0005g0160a0001c0001t0014g0174others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+11824A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417156 | ||||||
chr1:218417298
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510+11966C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417298 | ||||||
chr1:218417303
|
G | A | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.510+11971G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417303 | ||||||
chr1:218417313
|
G | A | 27 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0096others(24): Show | 27 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+11981G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417313 | ||||||
chr1:218417372
|
T | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+12040T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417372 | ||||||
chr1:218417430
|
A | G | 3 | a0001c0001t0011g0225a0001c0001t0028g0275a0001c0001t0028g0276 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+12098A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417430 | ||||||
chr1:218417531
|
G | T | 1 | a0001c0001t0065g0187 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.510+12199G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417531 | ||||||
chr1:218417705
|
T | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+12373T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417705 | ||||||
chr1:218417805
|
G | A | 1 | a0001c0001t0070g0132 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.510+12473G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417805 | ||||||
chr1:218417852
|
T | G | 5 | a0001c0001t0002g0112a0001c0001t0002g0195a0001c0001t0004g0233others(2): Show | 5 | HG01978.hp1 HG02056.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+12520T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417852 | ||||||
chr1:218417977
|
G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+12645G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417977 | ||||||
chr1:218418200
|
T | C | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+12868T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418200 | ||||||
chr1:218418281
|
G | A | 167 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(164): Show | 170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.510+12949G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418281 | ||||||
chr1:218418349
|
G | A | 1 | a0001c0001t0007g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.510+13017G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418349 | ||||||
chr1:218418423
|
G | A | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.510+13091G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418423 | ||||||
chr1:218418640
|
G | T | 5 | a0001c0001t0002g0156a0001c0001t0002g0198a0001c0001t0004g0026others(2): Show | 5 | NA18940.hp2 NA18993.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13308G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418640 | ||||||
chr1:218418704
|
G | C | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13372G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418704 | ||||||
chr1:218418773
|
G | A | 55 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(52): Show | 56 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(53): Show |
intron_variant | MODIFIER | c.510+13441G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418773 | ||||||
chr1:218418818
|
G | T | 2 | a0001c0001t0038g0229a0001c0001t0053g0058 | 2 | HG03669.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.510+13486G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418818 | ||||||
chr1:218418920
|
C | T | 1 | a0001c0001t0039g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.510+13588C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418920 | ||||||
chr1:218418932
|
T | C | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13600T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418932 | ||||||
chr1:218419192
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.510+13860T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419192 | ||||||
chr1:218419389
|
G | A | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.510+14057G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419389 | ||||||
chr1:218419528
|
T | C | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.510+14196T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419528 | ||||||
chr1:218419563
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.510+14231G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419563 | ||||||
chr1:218419645
|
A | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+14313A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419645 | ||||||
chr1:218419695
|
C | T | 101 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(98): Show | 103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.510+14363C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419695 | ||||||
chr1:218420080
|
G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-14002G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420080 | ||||||
chr1:218420478
|
A | T | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-13604A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420478 | ||||||
chr1:218420740
|
G | T | 3 | a0001c0001t0002g0173a0001c0001t0010g0020a0001c0001t0033g0044 | 3 | NA18986.hp2 NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.511-13342G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420740 | ||||||
chr1:218420887
|
GC | G | 3 | a0001c0001t0011g0225a0001c0001t0028g0275a0001c0001t0028g0276 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-13194delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420887 | ||||||
chr1:218421142
|
G | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0167 | 2 | HG01346.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.511-12940G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421142 | ||||||
chr1:218421246
|
T | C | 5 | a0001c0001t0011g0208a0001c0001t0038g0229a0001c0001t0051g0168others(2): Show | 5 | HG03471.hp1 HG03669.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-12836T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421246 | ||||||
chr1:218421373
|
G | GT | 49 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0085others(46): Show | 49 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.511-12694dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421373 | |||||
chr1:218421373
|
GT | G | 159 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(156): Show | 162 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.511-12694delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421373 | |||||
chr1:218421376
|
T | G | 1 | a0001c0001t0004g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.511-12706T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421376 | ||||||
chr1:218421377
|
T | G | 100 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(97): Show | 102 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-12705T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421377 | ||||||
chr1:218421406
|
A | AT | 52 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(49): Show | 53 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-12674dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421406 | |||||
chr1:218421413
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.511-12669A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421413 | ||||||
chr1:218421578
|
G | T | 169 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(166): Show | 172 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-12504G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421578 | ||||||
chr1:218421613
|
A | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-12469A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421613 | ||||||
chr1:218421653
|
TA | T | 10 | a0001c0001t0011g0208a0001c0001t0021g0221a0001c0001t0021g0228others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-12421delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421653 | |||||
chr1:218421772
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511-12310C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421772 | ||||||
chr1:218421984
|
G | A | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-12098G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421984 | ||||||
chr1:218422019
|
G | C | 1 | a0001c0001t0030g0009 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.511-12063G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422019 | ||||||
chr1:218422244
|
G | A | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-11838G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422244 | ||||||
chr1:218422257
|
A | G | 1 | a0001c0001t0005g0113 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.511-11825A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422257 | ||||||
chr1:218422318
|
A | G | 1 | a0001c0001t0061g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.511-11764A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422318 | ||||||
chr1:218422373
|
A | G | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-11709A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422373 | ||||||
chr1:218422378
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.511-11704C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422378 | ||||||
chr1:218422458
|
C | T | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-11624C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422458 | ||||||
chr1:218422565
|
T | C | 1 | a0001c0001t0008g0182 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-11517T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422565 | ||||||
chr1:218422590
|
G | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-11492G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422590 | ||||||
chr1:218422769
|
C | T | 1 | a0001c0001t0007g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.511-11313C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422769 | ||||||
chr1:218422872
|
A | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-11210A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422872 | ||||||
chr1:218423119
|
A | G | 169 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(166): Show | 172 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-10963A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423119 | ||||||
chr1:218423299
|
G | T | 169 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(166): Show | 172 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-10783G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423299 | ||||||
chr1:218423411
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.511-10671T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423411 | ||||||
chr1:218423415
|
G | A | 1 | a0001c0001t0009g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.511-10667G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423415 | ||||||
chr1:218423657
|
C | T | 1 | a0001c0001t0048g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.511-10425C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423657 | ||||||
chr1:218423658
|
G | A | 2 | a0001c0001t0076g0281a0001c0001t0086g0213 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.511-10424G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423658 | ||||||
chr1:218423702
|
G | A | 172 | a0001c0001t0001g0103a0001c0001t0001g0151a0001c0001t0002g0056others(169): Show | 175 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(172): Show |
intron_variant | MODIFIER | c.511-10380G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423702 | ||||||
chr1:218423955
|
C | G | 169 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(166): Show | 172 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-10127C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423955 | ||||||
chr1:218423963
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511-10119C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423963 | ||||||
chr1:218423964
|
G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-10118G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423964 | ||||||
chr1:218424075
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-10007C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424075 | ||||||
chr1:218424290
|
G | A | 91 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(88): Show | 93 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.511-9792G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424290 | ||||||
chr1:218424517
|
C | T | 101 | a0001c0001t0001g0151a0001c0001t0002g0056a0001c0001t0002g0057others(98): Show | 103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-9565C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424517 | ||||||
chr1:218424747
|
G | T | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-9335G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424747 | ||||||
chr1:218424971
|
G | T | 1 | a0001c0001t0006g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.511-9111G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424971 | ||||||
chr1:218424986
|
C | G | 156 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(153): Show | 159 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.511-9096C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424986 | ||||||
chr1:218425042
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0152 | 3 | NA18974.hp1 NA19080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.511-9040A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425042 | ||||||
chr1:218425068
|
G | T | 157 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(154): Show | 160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.511-9014G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425068 | ||||||
chr1:218425127
|
A | T | 157 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(154): Show | 160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.511-8955A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425127 | ||||||
chr1:218425142
|
C | T | 167 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(164): Show | 170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.511-8940C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425142 | ||||||
chr1:218425235
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0039g0041 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.511-8847T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425235 | ||||||
chr1:218425276
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8806C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425276 | ||||||
chr1:218425313
|
T | C | 1 | a0001c0001t0067g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.511-8769T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425313 | ||||||
chr1:218425332
|
C | G | 5 | a0001c0001t0011g0208a0001c0001t0038g0229a0001c0001t0051g0168others(2): Show | 5 | HG03471.hp1 HG03669.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-8750C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425332 | ||||||
chr1:218425364
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511-8718C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425364 | ||||||
chr1:218425399
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-8683G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425399 | ||||||
chr1:218425455
|
C | T | 1 | a0001c0001t0012g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.511-8627C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425455 | ||||||
chr1:218425477
|
G | A | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8605G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425477 | ||||||
chr1:218425733
|
C | T | 1 | a0001c0001t0013g0245 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.511-8349C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425733 | ||||||
chr1:218425837
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.511-8245C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425837 | ||||||
chr1:218425850
|
A | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8232A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425850 | ||||||
chr1:218426047
|
G | A | 2 | a0001c0001t0051g0168a0001c0001t0052g0055 | 2 | HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.511-8035G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426047 | ||||||
chr1:218426252
|
C | G | 1 | a0001c0001t0090g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.511-7830C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426252 | ||||||
chr1:218426490
|
T | C | 3 | a0001c0001t0054g0186a0001c0001t0055g0149a0001c0001t0091g0012 | 3 | NA18967.hp2 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.511-7592T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426490 | ||||||
chr1:218426577
|
T | C | 7 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0074others(4): Show | 7 | HG02040.hp2 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-7505T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426577 | ||||||
chr1:218426756
|
A | G | 1 | a0001c0001t0038g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-7326A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426756 | ||||||
chr1:218426951
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0188a0001c0001t0003g0237 | 3 | HG00558.hp2 HG02523.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.511-7131C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426951 | ||||||
chr1:218427059
|
C | T | 1 | a0001c0001t0084g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-7023C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427059 | ||||||
chr1:218427077
|
C | T | 158 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(155): Show | 161 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.511-7005C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427077 | ||||||
chr1:218427477
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.511-6605C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427477 | ||||||
chr1:218427523
|
C | T | 1 | a0001c0001t0016g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.511-6559C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427523 | ||||||
chr1:218427581
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0009g0222a0001c0001t0029g0267others(1): Show | 4 | HG01169.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-6501G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427581 | ||||||
chr1:218427630
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0068others(282): Show | 289 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(286): Show |
intron_variant | MODIFIER | c.511-6452T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427630 | ||||||
chr1:218427641
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.511-6441A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427641 | ||||||
chr1:218427963
|
G | A | 52 | a0001c0001t0002g0056a0001c0001t0002g0071a0001c0001t0002g0092others(49): Show | 53 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-6119G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427963 | ||||||
chr1:218428563
|
GTT | G | 47 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(44): Show | 47 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.511-5516_511-5515d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428563 | |||||
chr1:218428622
|
G | C | 1 | a0001c0001t0007g0101 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.511-5460G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428622 | ||||||
chr1:218428739
|
C | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0138a0001c0001t0002g0179others(1): Show | 4 | HG00621.hp1 NA18949.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-5343C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428739 | ||||||
chr1:218428792
|
T | C | 56 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(53): Show | 56 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.511-5290T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428792 | ||||||
chr1:218428793
|
G | A | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-5289G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428793 | ||||||
chr1:218428972
|
C | CT | 95 | a0001c0001t0001g0061a0001c0001t0001g0097a0001c0001t0001g0103others(92): Show | 97 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.511-5086dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | |||||
chr1:218428972
|
C | CTT | 10 | a0001c0001t0001g0158a0001c0001t0002g0098a0001c0001t0002g0179others(7): Show | 10 | HG01891.hp1 HG02056.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-5087_511-5086d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | |||||
chr1:218428972
|
CT | C | 33 | a0001c0001t0003g0248a0001c0001t0005g0078a0001c0001t0005g0079others(30): Show | 33 | HG01258.hp1 HG01261.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.511-5086delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | |||||
chr1:218429058
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-5024G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429058 | ||||||
chr1:218429105
|
C | T | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-4977C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429105 | ||||||
chr1:218429229
|
C | A | 3 | a0001c0001t0005g0164a0001c0001t0009g0034a0001c0001t0009g0038 | 3 | HG03017.hp2 HG04228.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.511-4853C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429229 | ||||||
chr1:218429250
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.511-4832G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429250 | ||||||
chr1:218429379
|
A | G | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-4703A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429379 | ||||||
chr1:218429518
|
C | G | 3 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0074 | 3 | NA18964.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.511-4564C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429518 | ||||||
chr1:218429746
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-4336C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429746 | ||||||
chr1:218429918
|
T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-4164T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429918 | ||||||
chr1:218430132
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511-3950C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430132 | ||||||
chr1:218430251
|
G | A | 6 | a0001c0001t0003g0022a0001c0001t0027g0270a0001c0001t0031g0284others(3): Show | 6 | HG02717.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-3831G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430251 | ||||||
chr1:218430264
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-3818G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430264 | ||||||
chr1:218430274
|
A | T | 1 | a0001c0001t0004g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.511-3808A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430274 | ||||||
chr1:218430401
|
A | G | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-3681A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430401 | ||||||
chr1:218430500
|
G | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-3582G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430500 | ||||||
chr1:218430570
|
C | G | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.511-3512C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430570 | ||||||
chr1:218430654
|
G | T | 1 | a0001c0001t0016g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.511-3428G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430654 | ||||||
chr1:218430732
|
C | T | 1 | a0001c0001t0081g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.511-3350C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430732 | ||||||
chr1:218430946
|
G | A | 8 | a0001c0001t0005g0164a0001c0001t0009g0034a0001c0001t0009g0038others(5): Show | 8 | HG01261.hp2 HG02630.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-3136G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430946 | ||||||
chr1:218431050
|
C | A | 53 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(50): Show | 54 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.511-3032C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431050 | ||||||
chr1:218431124
|
A | G | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.511-2958A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431124 | ||||||
chr1:218431273
|
A | G | 1 | a0001c0002t0002g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.511-2809A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431273 | ||||||
chr1:218431284
|
C | T | 2 | a0001c0001t0002g0071a0001c0001t0068g0171 | 2 | NA18944.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.511-2798C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431284 | ||||||
chr1:218431336
|
G | A | 158 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(155): Show | 161 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.511-2746G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431336 | ||||||
chr1:218431367
|
C | T | 90 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(87): Show | 92 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.511-2715C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431367 | ||||||
chr1:218431566
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0029g0266 | 2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.511-2516A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431566 | ||||||
chr1:218431923
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.511-2159A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431923 | ||||||
chr1:218431963
|
T | C | 53 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(50): Show | 54 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.511-2119T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431963 | ||||||
chr1:218432117
|
T | C | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.511-1965T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432117 | ||||||
chr1:218432119
|
G | A | 158 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(155): Show | 161 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.511-1963G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432119 | ||||||
chr1:218432159
|
A | G | 1 | a0001c0001t0038g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-1923A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432159 | ||||||
chr1:218432262
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-1820A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432262 | ||||||
chr1:218432267
|
G | A | 168 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(165): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.511-1815G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432267 | ||||||
chr1:218432270
|
G | A | 2 | a0001c0001t0009g0222a0001c0001t0090g0011 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.511-1812G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432270 | ||||||
chr1:218432293
|
T | C | 101 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(98): Show | 103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-1789T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432293 | ||||||
chr1:218432379
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.511-1703G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432379 | ||||||
chr1:218432411
|
A | C | 1 | a0001c0001t0050g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.511-1671A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432411 | ||||||
chr1:218432437
|
C | A | 3 | a0001c0001t0011g0225a0001c0001t0028g0275a0001c0001t0028g0276 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-1645C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432437 | ||||||
chr1:218432450
|
T | C | 1 | a0001c0001t0083g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-1632T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432450 | ||||||
chr1:218432504
|
A | G | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-1578A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432504 | ||||||
chr1:218432608
|
C | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1474C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432608 | ||||||
chr1:218432614
|
T | C | 95 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(92): Show | 97 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.511-1468T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432614 | ||||||
chr1:218432664
|
A | G | 3 | a0001c0001t0011g0225a0001c0001t0028g0275a0001c0001t0028g0276 | 3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-1418A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432664 | ||||||
chr1:218432810
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.511-1272C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432810 | ||||||
chr1:218432859
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-1223C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432859 | ||||||
chr1:218432881
|
G | A | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-1201G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432881 | ||||||
chr1:218433030
|
T | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-1052T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433030 | ||||||
chr1:218433072
|
A | AT | 5 | a0001c0001t0011g0208a0001c0001t0011g0226a0001c0001t0020g0004others(2): Show | 6 | HG01433.hp2 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-1002dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218433072 | |||||
chr1:218433126
|
T | G | 4 | a0001c0001t0038g0229a0001c0001t0051g0168a0001c0001t0052g0055others(1): Show | 4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-956T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433126 | ||||||
chr1:218433138
|
G | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-944G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433138 | ||||||
chr1:218433405
|
G | A | 6 | a0001c0001t0005g0160a0001c0001t0014g0174a0001c0001t0014g0191others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-677G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433405 | ||||||
chr1:218433533
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-549A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433533 | ||||||
chr1:218433578
|
A | C | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-504A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433578 | ||||||
chr1:218433606
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0169 | 2 | HG00140.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.511-476G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433606 | ||||||
chr1:218433955
|
C | A | 2 | a0001c0001t0005g0078a0001c0001t0005g0079 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.511-127C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433955 | ||||||
chr1:218434009
|
G | C | 5 | a0001c0001t0002g0204a0001c0001t0013g0211a0001c0001t0013g0212others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-73G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218434009 | ||||||
chr1:218434221
|
A | C | 3 | a0001c0001t0001g0103a0001c0001t0003g0255a0001c0001t0085g0262 | 3 | HG02109.hp2 HG02257.hp2 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.643+7A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 3/6 | chr1 | 218434221 | ||||||
chr1:218434506
|
A | G | 5 | a0001c0001t0002g0204a0001c0001t0013g0211a0001c0001t0013g0212others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+58A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434506 | ||||||
chr1:218434519
|
T | C | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.754+71T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434519 | ||||||
chr1:218434781
|
G | T | 5 | a0001c0001t0011g0208a0001c0001t0011g0226a0001c0001t0020g0004others(2): Show | 6 | HG01433.hp2 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+333G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434781 | ||||||
chr1:218434782
|
A | G | 1 | a0001c0001t0066g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.754+334A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434782 | ||||||
chr1:218434966
|
A | G | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.754+518A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434966 | ||||||
chr1:218435180
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.754+732C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435180 | ||||||
chr1:218435215
|
A | T | 1 | a0001c0001t0002g0127 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.755-755A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435215 | ||||||
chr1:218435300
|
G | C | 1 | a0001c0001t0009g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.755-670G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435300 | ||||||
chr1:218435764
|
C | A | 1 | a0001c0001t0032g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755-206C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435764 | ||||||
chr1:218436224
|
T | G | 1 | a0001c0001t0003g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.932+77T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436224 | ||||||
chr1:218436259
|
T | G | 1 | a0001c0001t0075g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.932+112T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436259 | ||||||
chr1:218436360
|
A | G | 168 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(165): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.932+213A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436360 | ||||||
chr1:218436394
|
G | A | 2 | a0001c0001t0044g0238a0001c0001t0066g0134 | 2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.932+247G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436394 | ||||||
chr1:218436586
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.932+439C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436586 | ||||||
chr1:218436730
|
A | G | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.932+583A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436730 | ||||||
chr1:218436912
|
C | T | 168 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(165): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.933-431C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436912 | ||||||
chr1:218437022
|
A | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.933-321A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218437022 | ||||||
chr1:218437092
|
C | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-251C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218437092 | ||||||
chr1:218437320
|
C | CT | 6 | a0001c0001t0001g0103a0001c0001t0003g0255a0001c0001t0003g0256others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.933-6dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 218437320 | |||||
chr1:218437320
|
CT | C | 157 | a0001c0001t0001g0084a0001c0001t0001g0140a0001c0001t0002g0056others(154): Show | 160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
splice_region_variant&intron_variant | LOW | c.933-6delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 218437320 | |||||
chr1:218437577
|
T | C | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1086+81T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437577 | ||||||
chr1:218437694
|
C | T | 3 | a0001c0001t0050g0205a0001c0001t0057g0141a0001c0001t0063g0086 | 3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1086+198C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437694 | ||||||
chr1:218437839
|
C | A | 24 | a0001c0001t0005g0110a0001c0001t0005g0113a0001c0001t0005g0170others(21): Show | 24 | HG01258.hp1 HG01496.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.1086+343C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437839 | ||||||
chr1:218437879
|
G | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1086+383G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437879 | ||||||
chr1:218438031
|
A | G | 1 | a0001c0001t0005g0110 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1086+535A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438031 | ||||||
chr1:218438061
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1086+565T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438061 | ||||||
chr1:218438133
|
C | G | 46 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(43): Show | 46 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1086+637C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438133 | ||||||
chr1:218438281
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1086+785G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438281 | ||||||
chr1:218438387
|
A | G | 6 | a0001c0001t0003g0022a0001c0001t0027g0270a0001c0001t0031g0284others(3): Show | 6 | HG02717.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+891A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438387 | ||||||
chr1:218438536
|
A | G | 235 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(232): Show | 238 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.1086+1040A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438536 | ||||||
chr1:218438558
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1086+1062G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438558 | ||||||
chr1:218438666
|
A | G | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1086+1170A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438666 | ||||||
chr1:218438670
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1086+1174C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438670 | ||||||
chr1:218438830
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1086+1334C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438830 | ||||||
chr1:218438875
|
G | A | 1 | a0001c0001t0059g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1086+1379G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438875 | ||||||
chr1:218438935
|
C | T | 4 | a0001c0001t0038g0229a0001c0001t0051g0168a0001c0001t0052g0055others(1): Show | 4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+1439C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438935 | ||||||
chr1:218439002
|
G | A | 5 | a0001c0001t0004g0223a0001c0001t0004g0224a0001c0001t0004g0252others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1086+1506G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439002 | ||||||
chr1:218439107
|
CA | C | 107 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0081others(104): Show | 108 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(105): Show |
intron_variant | MODIFIER | c.1086+1631delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218439107 | |||||
chr1:218439107
|
CAA | C | 111 | a0001c0001t0001g0103a0001c0001t0002g0056a0001c0001t0002g0057others(108): Show | 113 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.1086+1630_1086+163 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218439107 | |||||
chr1:218439165
|
C | T | 2 | a0001c0001t0006g0089a0001c0001t0006g0145 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1086+1669C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439165 | ||||||
chr1:218439283
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1086+1787G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439283 | ||||||
chr1:218439336
|
G | A | 2 | a0001c0001t0003g0255a0001c0001t0085g0262 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1086+1840G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439336 | ||||||
chr1:218439502
|
G | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-1702G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439502 | ||||||
chr1:218439606
|
C | T | 2 | a0001c0001t0007g0176a0001c0001t0065g0187 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1087-1598C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439606 | ||||||
chr1:218440175
|
C | T | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-1029C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440175 | ||||||
chr1:218440278
|
T | A | 7 | a0001c0001t0038g0229a0001c0001t0051g0168a0001c0001t0052g0055others(4): Show | 7 | HG03669.hp1 HG04228.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1087-926T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440278 | ||||||
chr1:218440345
|
CT | C | 168 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0071others(165): Show | 171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.1087-847delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440345 | |||||
chr1:218440353
|
T | C | 1 | a0001c0001t0077g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-851T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440353 | ||||||
chr1:218440571
|
A | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0003g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-633A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440571 | ||||||
chr1:218440680
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0197a0001c0001t0041g0249 | 3 | HG00738.hp1 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1087-524A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440680 | ||||||
chr1:218440829
|
TA | T | 4 | a0001c0001t0001g0077a0001c0001t0003g0219a0001c0001t0016g0062others(1): Show | 4 | HG01169.hp1 HG02486.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087-373delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440829 | |||||
chr1:218440924
|
G | GA | 56 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0110others(53): Show | 57 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(54): Show |
intron_variant | MODIFIER | c.1087-276dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440924 | |||||
chr1:218440987
|
T | C | 1 | a0001c0001t0003g0232 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1087-217T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440987 | ||||||
chr1:218440997
|
G | A | 5 | a0001c0001t0021g0221a0001c0001t0021g0228a0001c0001t0050g0205others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-207G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440997 | ||||||
chr1:218441163
|
G | A | 1 | a0001c0001t0009g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1087-41G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218441163 |