geneid | 200424 |
---|---|
ensemblid | ENSG00000187605.16 |
hgncid | 28313 |
symbol | TET3 |
name | tet methylcytosine dioxygenase 3 |
refseq_nuc | NM_001287491.2 |
refseq_prot | NP_001274420.1 |
ensembl_nuc | ENST00000409262.8 |
ensembl_prot | ENSP00000386869.3 |
mane_status | MANE Select |
chr | chr2 |
start | 73984910 |
end | 74108176 |
strand | + |
ver | v1.2 |
region | chr2:73984910-74108176 |
region5000 | chr2:73979910-74113176 |
regionname0 | TET3_chr2_73984910_74108176 |
regionname5000 | TET3_chr2_73979910_74113176 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1795 | 241 | 72 | 49 | 86 | 10 | 22 | 57 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0002 | 0/0 | 1795 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0003 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0004 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0005 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0006 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0007 | 0/0 | 1795 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0008 | 0/0 | 1795 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5388 | 119 | 10 | 23 | 64 | 6 | 14 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0002 | 0/0 | 5388 | 90 | 41 | 20 | 19 | 4 | 6 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0003 | 0/0 | 5388 | 8 | 6 | 2 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0004 | 0/0 | 5388 | 5 | 5 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0005 | 0/0 | 5388 | 5 | 0 | 3 | 0 | 2 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0006 | 0/0 | 5388 | 3 | 0 | 3 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0007 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0008 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0009 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0010 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0011 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0012 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0013 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0014 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0015 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0016 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0017 | 0/0 | 5388 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0018 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0019 | 0/0 | 5388 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0020 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0021 | 0/0 | 5388 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0022 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0023 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0024 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
c0025 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 6670 | 66 | 9 | 18 | 22 | 6 | 10 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0002 | 0/0 | 6670 | 25 | 6 | 4 | 8 | 4 | 3 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0003 | 0/0 | 6670 | 22 | 3 | 5 | 14 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0004 | 0/0 | 6669 | 19 | 0 | 4 | 9 | 2 | 4 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0005 | 0/0 | 6670 | 18 | 4 | 7 | 5 | 0 | 2 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0006 | 0/0 | 6670 | 12 | 0 | 2 | 10 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0007 | 0/0 | 6670 | 8 | 0 | 1 | 7 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0008 | 0/0 | 6670 | 6 | 2 | 4 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0009 | 0/0 | 6669 | 4 | 0 | 0 | 4 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0010 | 0/0 | 6667 | 4 | 4 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0011 | 0/0 | 6671 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0012 | 0/0 | 6668 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0013 | 0/0 | 6667 | 3 | 2 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0014 | 0/0 | 6668 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0015 | 0/0 | 6674 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0016 | 0/0 | 6670 | 2 | 0 | 1 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0017 | 0/0 | 6669 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0018 | 0/0 | 6670 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0019 | 0/0 | 6673 | 2 | 1 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0020 | 0/0 | 6669 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0021 | 0/0 | 6670 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0022 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0023 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0024 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0025 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0026 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0027 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0028 | 0/0 | 6659 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0029 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0030 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0031 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0032 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0033 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0034 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0035 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0036 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0037 | 0/0 | 6670 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0038 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0039 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0040 | 0/0 | 6670 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0041 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0042 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0043 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0044 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0045 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0046 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0047 | 0/0 | 6670 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0048 | 0/0 | 6659 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0049 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0050 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0051 | 0/0 | 6669 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0052 | 0/0 | 6669 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0053 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0054 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0055 | 0/0 | 6670 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0056 | 0/0 | 6674 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0057 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0058 | 0/0 | 6723 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0059 | 0/0 | 6724 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0060 | 0/0 | 6649 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0061 | 1/0 | 6673 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0062 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
t0063 | 0/0 | 6670 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5388 | 119 | 10 | 23 | 64 | 6 | 14 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002 | 0/0 | 5388 | 90 | 41 | 20 | 19 | 4 | 6 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003 | 0/0 | 5388 | 8 | 6 | 2 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0004 | 0/0 | 5388 | 5 | 5 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0006 | 0/0 | 5388 | 3 | 0 | 3 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0007 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0008 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0009 | 0/0 | 5388 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0010 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0013 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0014 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0015 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0016 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0017 | 0/0 | 5388 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0018 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0019 | 0/0 | 5388 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0020 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0021 | 0/0 | 5388 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0002c0005 | 0/0 | 5388 | 5 | 0 | 3 | 0 | 2 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0003c0025 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0004c0022 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0005c0011 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0006c0012 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0007c0023 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0008c0024 | 0/0 | 5388 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 12057 | 51 | 3 | 13 | 20 | 5 | 9 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0002 | 0/0 | 12057 | 12 | 2 | 0 | 8 | 1 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0003 | 0/0 | 12057 | 2 | 1 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0004 | 0/0 | 12056 | 12 | 0 | 3 | 8 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0005 | 0/0 | 12057 | 10 | 0 | 5 | 4 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0006 | 0/0 | 12057 | 7 | 0 | 0 | 7 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0007 | 0/0 | 12057 | 6 | 0 | 0 | 6 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0009 | 0/0 | 12056 | 4 | 0 | 0 | 4 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0019 | 0/0 | 12060 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0020 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0021 | 0/0 | 12057 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0022 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0032 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0037 | 0/0 | 12057 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0040 | 0/0 | 12057 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0041 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0047 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0051 | 0/0 | 12056 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0058 | 0/0 | 12110 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0059 | 0/0 | 12111 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0061 | 1/0 | 12060 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0001t0063 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0001 | 0/0 | 12057 | 9 | 4 | 3 | 0 | 1 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0002 | 0/0 | 12057 | 4 | 0 | 1 | 0 | 1 | 2 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0003 | 0/0 | 12057 | 19 | 1 | 5 | 13 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0004 | 0/0 | 12056 | 5 | 0 | 1 | 0 | 2 | 2 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0005 | 0/0 | 12057 | 4 | 3 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0006 | 0/0 | 12057 | 5 | 0 | 2 | 3 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0007 | 0/0 | 12057 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0008 | 0/0 | 12057 | 6 | 2 | 4 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0011 | 0/0 | 12058 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0012 | 0/0 | 12055 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0013 | 0/0 | 12054 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0014 | 0/0 | 12055 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0015 | 0/0 | 12061 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0016 | 0/0 | 12057 | 2 | 0 | 1 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0017 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0018 | 0/0 | 12057 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0019 | 0/0 | 12060 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0020 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0023 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0024 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0026 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0028 | 0/0 | 12046 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0035 | 0/0 | 12055 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0036 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0038 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0039 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0042 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0045 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0046 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0048 | 0/0 | 12046 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0052 | 0/0 | 12056 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0053 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0055 | 0/0 | 12057 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0056 | 0/0 | 12061 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0057 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0060 | 0/0 | 12036 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0002t0062 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003t0010 | 0/0 | 12054 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003t0013 | 0/0 | 12054 | 2 | 1 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003t0017 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003t0029 | 0/0 | 12054 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0003t0050 | 0/0 | 12054 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0004t0002 | 0/0 | 12057 | 3 | 3 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0004t0003 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0004t0025 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0006t0001 | 0/0 | 12057 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0006t0005 | 0/0 | 12057 | 2 | 0 | 2 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0007t0010 | 0/0 | 12054 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0007t0033 | 0/0 | 12055 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0008t0001 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0008t0002 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0009t0005 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0009t0034 | 0/0 | 12056 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0010t0004 | 0/0 | 12056 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0013t0054 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0014t0044 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0015t0043 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0016t0001 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0017t0001 | 0/0 | 12057 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0018t0031 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0019t0004 | 0/0 | 12056 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0020t0007 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0001c0021t0005 | 0/0 | 12057 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0002c0005t0002 | 0/0 | 12057 | 5 | 0 | 3 | 0 | 2 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0003c0025t0030 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0004c0022t0049 | 0/0 | 12057 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0005c0011t0011 | 0/0 | 12058 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0006c0012t0027 | 0/0 | 12055 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0007c0023t0001 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
a0008c0024t0001 | 0/0 | 12057 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | copy fasta | chr2 | 73979910 | 74113176 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0009g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0019g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0020g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0021g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0021g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0022g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0032g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0037g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0040g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0041g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0047g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0051g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0058g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0059g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0061g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0001t0063g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0012g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0014g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0015g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0016g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0016g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0020g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0023g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0024g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0028g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0035g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0036g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0038g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0039g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0042g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0045g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0046g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0048g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0052g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0053g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0055g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0056g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0057g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0060g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0002t0062g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0013g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0013g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0029g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0003t0050g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0004t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0004t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0004t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0004t0025g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0006t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0006t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0006t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0007t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0007t0033g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0008t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0009t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0009t0034g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0010t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0013t0054g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0014t0044g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0015t0043g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0016t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0017t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0018t0031g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0019t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0020t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0001c0021t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0002c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0002c0005t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0002c0005t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0002c0005t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0002c0005t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0003c0025t0030g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0004c0022t0049g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0005c0011t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0006c0012t0027g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0007c0023t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
a0008c0024t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0080 | EUR | GBR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00280 | hp1 | a0002 | c0005 | t0002 | g0178 | EUR | FIN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0175 | EUR | FIN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0231 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00558 | hp2 | a0001 | c0002 | t0006 | g0211 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00609 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00642 | hp1 | a0001 | c0006 | t0005 | g0248 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0065 | EAS | CHS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00735 | hp2 | a0001 | c0003 | t0029 | g0242 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00738 | hp2 | a0001 | c0001 | t0037 | g0078 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00741 | hp1 | a0002 | c0005 | t0002 | g0149 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG00741 | hp2 | a0001 | c0002 | t0008 | g0109 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01081 | hp2 | a0002 | c0005 | t0002 | g0127 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01106 | hp1 | a0001 | c0001 | t0019 | g0119 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01167 | hp1 | a0001 | c0002 | t0008 | g0015 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01169 | hp1 | a0001 | c0002 | t0008 | g0018 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0249 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0230 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01192 | hp1 | a0001 | c0003 | t0013 | g0203 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01192 | hp2 | a0001 | c0002 | t0035 | g0092 | AMR | PUR | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01255 | hp2 | a0001 | c0002 | t0007 | g0174 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0209 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01258 | hp2 | a0001 | c0002 | t0003 | g0215 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01261 | hp1 | a0002 | c0005 | t0002 | g0179 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01261 | hp2 | a0001 | c0002 | t0008 | g0086 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01346 | hp1 | a0001 | c0002 | t0006 | g0217 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0132 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01433 | hp2 | a0001 | c0006 | t0005 | g0250 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01496 | hp1 | a0001 | c0002 | t0052 | g0182 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0129 | EUR | IBS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01515 | hp2 | a0002 | c0005 | t0002 | g0126 | EUR | IBS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | IBS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0130 | EUR | IBS | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01884 | hp1 | a0001 | c0002 | t0005 | g0072 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01884 | hp2 | a0001 | c0002 | t0012 | g0189 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01928 | hp1 | a0001 | c0006 | t0001 | g0251 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01928 | hp2 | a0001 | c0002 | t0003 | g0216 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01934 | hp1 | a0001 | c0002 | t0016 | g0228 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0070 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01943 | hp2 | a0001 | c0002 | t0006 | g0218 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0197 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02055 | hp2 | a0001 | c0001 | t0021 | g0191 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02074 | hp2 | a0001 | c0001 | t0058 | g0024 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02080 | hp1 | a0001 | c0001 | t0047 | g0097 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02083 | hp1 | a0001 | c0018 | t0031 | g0062 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02083 | hp2 | a0008 | c0024 | t0001 | g0046 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02145 | hp1 | a0001 | c0003 | t0010 | g0003 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02165 | hp1 | a0001 | c0001 | t0009 | g0104 | EAS | CDX | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02257 | hp1 | a0001 | c0003 | t0017 | g0106 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02257 | hp2 | a0001 | c0002 | t0020 | g0184 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02258 | hp2 | a0001 | c0002 | t0039 | g0246 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02273 | hp2 | a0001 | c0017 | t0001 | g0031 | AMR | PEL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02280 | hp1 | a0001 | c0001 | t0063 | g0221 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02280 | hp2 | a0001 | c0002 | t0042 | g0013 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0120 | EAS | KHV | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0155 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02615 | hp1 | a0001 | c0004 | t0002 | g0006 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02615 | hp2 | a0001 | c0002 | t0038 | g0185 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02622 | hp1 | a0001 | c0002 | t0023 | g0220 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02630 | hp1 | a0001 | c0002 | t0014 | g0223 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02630 | hp2 | a0001 | c0014 | t0044 | g0004 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02647 | hp1 | a0001 | c0013 | t0054 | g0170 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02647 | hp2 | a0001 | c0009 | t0034 | g0167 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02683 | hp1 | a0001 | c0002 | t0004 | g0133 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02683 | hp2 | a0001 | c0001 | t0040 | g0049 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02717 | hp1 | a0001 | c0002 | t0011 | g0206 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02723 | hp1 | a0001 | c0002 | t0012 | g0204 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02723 | hp2 | a0001 | c0004 | t0003 | g0240 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02735 | hp1 | a0001 | c0002 | t0055 | g0145 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0144 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0074 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02809 | hp2 | a0001 | c0008 | t0001 | g0142 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02886 | hp1 | a0001 | c0002 | t0045 | g0138 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02886 | hp2 | a0001 | c0002 | t0015 | g0238 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02895 | hp1 | a0001 | c0002 | t0014 | g0001 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02896 | hp1 | a0001 | c0002 | t0046 | g0169 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02896 | hp2 | a0001 | c0002 | t0018 | g0139 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02897 | hp1 | a0001 | c0002 | t0014 | g0001 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02897 | hp2 | a0001 | c0002 | t0018 | g0137 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02922 | hp1 | a0001 | c0002 | t0048 | g0002 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02970 | hp1 | a0001 | c0002 | t0057 | g0073 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03017 | hp1 | a0001 | c0001 | t0051 | g0025 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03041 | hp1 | a0001 | c0007 | t0033 | g0134 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03041 | hp2 | a0001 | c0002 | t0028 | g0239 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03130 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03130 | hp2 | a0001 | c0003 | t0010 | g0016 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03139 | hp1 | a0001 | c0002 | t0017 | g0094 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03195 | hp1 | a0001 | c0002 | t0008 | g0019 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03195 | hp2 | a0001 | c0004 | t0025 | g0237 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03453 | hp2 | a0001 | c0016 | t0001 | g0105 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03486 | hp1 | a0001 | c0002 | t0013 | g0236 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03486 | hp2 | a0001 | c0009 | t0005 | g0168 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03516 | hp1 | a0001 | c0015 | t0043 | g0136 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03516 | hp2 | a0001 | c0002 | t0012 | g0188 | AFR | ESN | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03540 | hp2 | a0001 | c0002 | t0026 | g0205 | AFR | GWD | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03579 | hp1 | a0001 | c0002 | t0053 | g0020 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03579 | hp2 | a0003 | c0025 | t0030 | g0036 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03710 | hp2 | a0001 | c0021 | t0005 | g0160 | SAS | PJL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03834 | hp2 | a0001 | c0019 | t0004 | g0035 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18522 | hp1 | a0001 | c0002 | t0011 | g0222 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18522 | hp2 | a0006 | c0012 | t0027 | g0190 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | CHB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | CHB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18906 | hp1 | a0001 | c0008 | t0002 | g0148 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18906 | hp2 | a0001 | c0003 | t0013 | g0244 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18957 | hp2 | a0001 | c0001 | t0022 | g0063 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18962 | hp2 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18974 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18978 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18978 | hp2 | a0007 | c0023 | t0001 | g0026 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18989 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18989 | hp2 | a0001 | c0001 | t0059 | g0023 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18990 | hp2 | a0001 | c0020 | t0007 | g0147 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18999 | hp1 | a0001 | c0002 | t0006 | g0232 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19000 | hp2 | a0001 | c0002 | t0006 | g0195 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0012 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19009 | hp1 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19009 | hp2 | a0001 | c0001 | t0041 | g0042 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19030 | hp1 | a0001 | c0007 | t0010 | g0171 | AFR | LWK | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19030 | hp2 | a0004 | c0022 | t0049 | g0177 | AFR | LWK | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19043 | hp1 | a0001 | c0002 | t0062 | g0187 | AFR | LWK | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0140 | AFR | LWK | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19054 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19066 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19070 | hp2 | a0001 | c0002 | t0036 | g0089 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19078 | hp1 | a0001 | c0002 | t0016 | g0193 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19079 | hp2 | a0001 | c0001 | t0032 | g0058 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19083 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19083 | hp2 | a0001 | c0010 | t0004 | g0166 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19240 | hp1 | a0005 | c0011 | t0011 | g0235 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA19240 | hp2 | a0001 | c0002 | t0056 | g0090 | AFR | YRI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20129 | hp1 | a0001 | c0003 | t0050 | g0131 | AFR | ASW | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20129 | hp2 | a0001 | c0002 | t0019 | g0186 | AFR | ASW | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | GIH | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02559 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG02559 | hp2 | a0001 | c0002 | t0024 | g0213 | AFR | ACB | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03471 | hp1 | a0001 | c0002 | t0060 | g0245 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG03471 | hp2 | a0001 | c0002 | t0015 | g0243 | AFR | MSL | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG06807 | hp1 | a0001 | c0001 | t0020 | g0095 | AFR | USA | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
HG06807 | hp2 | a0001 | c0002 | t0008 | g0017 | AFR | USA | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20300 | hp1 | a0001 | c0003 | t0010 | g0107 | AFR | USA | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
NA20300 | hp2 | a0001 | c0001 | t0021 | g0192 | AFR | USA | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0143 | REF | REF | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0061 | g0110 | REF | REF | TET3_chr2_73979910_74113176 | TET3 | chr2 | 73979910 | 74113176 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74047194
|
C | T | 1 | a0003 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1277C>T | p.Pro426Leu | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 1949/12060 | 1277/5388 | 426/1795 | chr2 | 74047194 | ||
chr2:74047202
|
C | T | 1 | a0002 | 5 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(2): Show |
missense_variant | MODERATE | c.1285C>T | p.Pro429Ser | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 1957/12060 | 1285/5388 | 429/1795 | chr2 | 74047202 | ||
chr2:74047413
|
C | G | 1 | a0008 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1496C>G | p.Pro499Arg | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2168/12060 | 1496/5388 | 499/1795 | chr2 | 74047413 | ||
chr2:74047617
|
T | C | 1 | a0003 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1700T>C | p.Val567Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2372/12060 | 1700/5388 | 567/1795 | chr2 | 74047617 | ||
chr2:74047842
|
C | G | 1 | a0007 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1925C>G | p.Ala642Gly | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2597/12060 | 1925/5388 | 642/1795 | chr2 | 74047842 | ||
chr2:74048006
|
A | G | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2089A>G | p.Thr697Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2761/12060 | 2089/5388 | 697/1795 | chr2 | 74048006 | ||
chr2:74048052
|
G | A | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.2135G>A | p.Arg712Gln | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2807/12060 | 2135/5388 | 712/1795 | chr2 | 74048052 | ||
chr2:74101314
|
G | A | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.4526G>A | p.Arg1509Gln | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5198/12060 | 4526/5388 | 1509/1795 | chr2 | 74101314 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74047288
|
C | T | 1 | a0001c0006 | 3 | HG00642.hp1 HG01433.hp2 HG01928.hp1 |
synonymous_variant | LOW | c.1371C>T | p.Pro457Pro | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2043/12060 | 1371/5388 | 457/1795 | chr2 | 74047288 | ||
chr2:74047465
|
G | A | 1 | a0001c0010 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1548G>A | p.Ser516Ser | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2220/12060 | 1548/5388 | 516/1795 | chr2 | 74047465 | ||
chr2:74048230
|
C | T | 1 | a0001c0021 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.2313C>T | p.Thr771Thr | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/12 | 2985/12060 | 2313/5388 | 771/1795 | chr2 | 74048230 | ||
chr2:74073590
|
T | C | 11 | a0001c0002a0001c0003a0001c0004others(8): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
synonymous_variant | LOW | c.2536T>C | p.Leu846Leu | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/12 | 3208/12060 | 2536/5388 | 846/1795 | chr2 | 74073590 | ||
chr2:74087955
|
C | T | 1 | a0001c0009 | 2 | HG02647.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.2805C>T | p.Leu935Leu | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/12 | 3477/12060 | 2805/5388 | 935/1795 | chr2 | 74087955 | ||
chr2:74093537
|
C | T | 1 | a0001c0015 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.3138C>T | p.Asn1046Asn | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/12 | 3810/12060 | 3138/5388 | 1046/1795 | chr2 | 74093537 | ||
chr2:74093588
|
C | T | 1 | a0001c0020 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.3189C>T | p.Phe1063Phe | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/12 | 3861/12060 | 3189/5388 | 1063/1795 | chr2 | 74093588 | ||
chr2:74099593
|
G | A | 1 | a0001c0016 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.3585G>A | p.Ala1195Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/12 | 4257/12060 | 3585/5388 | 1195/1795 | chr2 | 74099593 | ||
chr2:74100724
|
T | C | 1 | a0001c0017 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.3936T>C | p.Ser1312Ser | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4608/12060 | 3936/5388 | 1312/1795 | chr2 | 74100724 | ||
chr2:74101312
|
G | C | 5 | a0001c0003a0001c0007a0001c0013others(2): Show | 13 | HG00735.hp2 HG01192.hp1 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.4524G>C | p.Leu1508Leu | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5196/12060 | 4524/5388 | 1508/1795 | chr2 | 74101312 | ||
chr2:74101522
|
C | T | 2 | a0001c0013a0004c0022 | 2 | HG02647.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.4734C>T | p.Ala1578Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5406/12060 | 4734/5388 | 1578/1795 | chr2 | 74101522 | ||
chr2:74101651
|
G | A | 1 | a0001c0018 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.4863G>A | p.Ala1621Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5535/12060 | 4863/5388 | 1621/1795 | chr2 | 74101651 | ||
chr2:74101747
|
C | T | 3 | a0001c0014a0001c0015a0003c0025 | 3 | HG02630.hp2 HG03516.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.4959C>T | p.Gly1653Gly | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5631/12060 | 4959/5388 | 1653/1795 | chr2 | 74101747 | ||
chr2:74101939
|
G | A | 1 | a0001c0019 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.5151G>A | p.Ala1717Ala | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5823/12060 | 5151/5388 | 1717/1795 | chr2 | 74101939 | ||
chr2:74101960
|
G | A | 2 | a0001c0004a0001c0008 | 7 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
synonymous_variant | LOW | c.5172G>A | p.Gln1724Gln | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5844/12060 | 5172/5388 | 1724/1795 | chr2 | 74101960 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73984921
|
A | G | 2 | a0001c0001t0021a0001c0001t0063 | 3 | HG02055.hp2 HG02280.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-661A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | 1483 | chr2 | 73984921 | |||||
chr2:73984999
|
C | T | 1 | a0001c0002t0062 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-583C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | chr2 | 73984999 | ||||||
chr2:73985020
|
T | C | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
5_prime_UTR_variant | MODIFIER | c.-562T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | 1384 | chr2 | 73985020 | |||||
chr2:73985064
|
C | CGGCGGCG others(47): Show |
2 | a0001c0001t0058a0001c0001t0059 | 2 | HG02074.hp2 NA18989.hp2 |
5_prime_UTR_variant | MODIFIER | c.-478_-477insGCCGCG others(48): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | 1299 | INFO_REALIGN_3_PRIME | chr2 | 73985064 | ||||
chr2:73985070
|
CGGCGGCG others(14): Show |
C | 1 | a0001c0002t0060 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-502_-482delCGCGAC others(15): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | 1304 | INFO_REALIGN_3_PRIME | chr2 | 73985070 | ||||
chr2:73985131
|
G | A | 1 | a0001c0001t0022 | 1 | NA18957.hp2 | 5_prime_UTR_variant | MODIFIER | c.-451G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/12 | 1273 | chr2 | 73985131 | |||||
chr2:73986040
|
C | T | 1 | a0001c0002t0057 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-364C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/12 | 364 | chr2 | 73986040 | |||||
chr2:73986118
|
G | A | 22 | a0001c0001t0003a0001c0001t0006a0001c0001t0021others(19): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-286G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/12 | 286 | chr2 | 73986118 | |||||
chr2:73986133
|
C | G | 1 | a0001c0002t0014 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-271C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/12 | 271 | chr2 | 73986133 | |||||
chr2:73986133
|
C | T | 1 | a0001c0002t0056 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-271C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/12 | 271 | chr2 | 73986133 | |||||
chr2:73986208
|
G | A | 1 | a0003c0025t0030 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-196G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/12 | 196 | chr2 | 73986208 | |||||
chr2:74102240
|
C | T | 1 | a0001c0002t0055 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 64 | chr2 | 74102240 | |||||
chr2:74102352
|
G | A | 1 | a0001c0018t0031 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 176 | chr2 | 74102352 | |||||
chr2:74102444
|
G | C | 2 | a0001c0001t0009a0001c0001t0058 | 5 | HG02074.hp2 HG02080.hp2 HG02165.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*268G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 268 | chr2 | 74102444 | |||||
chr2:74102448
|
TC | T | 17 | a0001c0001t0004a0001c0001t0009a0001c0001t0051others(14): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*281delC | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 281 | INFO_REALIGN_3_PRIME | chr2 | 74102448 | ||||
chr2:74102455
|
C | T | 2 | a0001c0001t0020a0001c0002t0020 | 2 | HG02257.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*279C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 279 | chr2 | 74102455 | |||||
chr2:74102527
|
G | A | 1 | a0004c0022t0049 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 351 | chr2 | 74102527 | |||||
chr2:74102542
|
A | G | 2 | a0001c0002t0012a0001c0002t0014 | 6 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 366 | chr2 | 74102542 | |||||
chr2:74102660
|
C | A | 1 | a0001c0001t0032 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 484 | chr2 | 74102660 | |||||
chr2:74102665
|
A | G | 1 | a0001c0002t0062 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 489 | chr2 | 74102665 | |||||
chr2:74102958
|
T | G | 2 | a0001c0003t0050a0001c0007t0033 | 2 | HG03041.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*782T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 782 | chr2 | 74102958 | |||||
chr2:74103090
|
G | A | 1 | a0001c0009t0034 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 914 | chr2 | 74103090 | |||||
chr2:74103368
|
C | T | 4 | a0001c0001t0019a0001c0002t0019a0001c0002t0028others(1): Show | 4 | HG01106.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1192C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1192 | chr2 | 74103368 | |||||
chr2:74103525
|
C | T | 1 | a0001c0001t0047 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1349 | chr2 | 74103525 | |||||
chr2:74103666
|
C | T | 12 | a0001c0002t0011a0001c0002t0013a0001c0003t0010others(9): Show | 16 | HG00735.hp2 HG01192.hp1 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1490C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1490 | chr2 | 74103666 | |||||
chr2:74103824
|
A | G | 1 | a0001c0002t0046 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1648A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1648 | chr2 | 74103824 | |||||
chr2:74103891
|
TTG | T | 15 | a0001c0002t0011a0001c0002t0012a0001c0002t0013others(12): Show | 23 | HG00735.hp2 HG01192.hp1 HG01192.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1717_*1718delGT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1717 | INFO_REALIGN_3_PRIME | chr2 | 74103891 | ||||
chr2:74103965
|
C | T | 6 | a0001c0002t0008a0001c0002t0018a0001c0002t0045others(3): Show | 12 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1789C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1789 | chr2 | 74103965 | |||||
chr2:74103993
|
G | A | 1 | a0001c0001t0059 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1817G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 1817 | chr2 | 74103993 | |||||
chr2:74104192
|
C | T | 21 | a0001c0001t0021a0001c0002t0011a0001c0002t0012others(18): Show | 30 | HG00735.hp2 HG01192.hp1 HG01192.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2016C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 2016 | chr2 | 74104192 | |||||
chr2:74104336
|
C | G | 1 | a0001c0014t0044 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2160C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 2160 | chr2 | 74104336 | |||||
chr2:74104638
|
T | A | 1 | a0001c0002t0036 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2462T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 2462 | chr2 | 74104638 | |||||
chr2:74104832
|
G | A | 4 | a0001c0002t0012a0001c0002t0014a0001c0002t0023others(1): Show | 8 | HG01192.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2656G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 2656 | chr2 | 74104832 | |||||
chr2:74104871
|
T | G | 1 | a0001c0001t0037 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2695T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 2695 | chr2 | 74104871 | |||||
chr2:74105284
|
C | T | 1 | a0001c0001t0041 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3108C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3108 | chr2 | 74105284 | |||||
chr2:74105342
|
G | A | 1 | a0001c0001t0051 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3166G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3166 | chr2 | 74105342 | |||||
chr2:74105654
|
TTTTGGGA others(7): Show |
T | 2 | a0001c0002t0028a0001c0002t0048 | 2 | HG02922.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3483_*3496delGGAA others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3483 | INFO_REALIGN_3_PRIME | chr2 | 74105654 | ||||
chr2:74105698
|
AAAGC | A | 81 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(78): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*3526_*3529delCAAG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3526 | INFO_REALIGN_3_PRIME | chr2 | 74105698 | ||||
chr2:74106093
|
C | CT | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*3927dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3928 | INFO_REALIGN_3_PRIME | chr2 | 74106093 | ||||
chr2:74106141
|
C | T | 1 | a0001c0003t0029 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3965C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 3965 | chr2 | 74106141 | |||||
chr2:74106177
|
T | C | 1 | a0001c0002t0039 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4001T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4001 | chr2 | 74106177 | |||||
chr2:74106495
|
C | T | 1 | a0001c0001t0040 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4319C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4319 | chr2 | 74106495 | |||||
chr2:74106571
|
A | C | 1 | a0001c0002t0023 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4395A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4395 | chr2 | 74106571 | |||||
chr2:74106623
|
G | A | 1 | a0001c0002t0039 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4447G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4447 | chr2 | 74106623 | |||||
chr2:74106855
|
T | C | 1 | a0001c0002t0042 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4679T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4679 | chr2 | 74106855 | |||||
chr2:74107080
|
A | T | 1 | a0001c0002t0024 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4904A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 4904 | chr2 | 74107080 | |||||
chr2:74107185
|
C | T | 1 | a0001c0002t0062 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5009C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5009 | chr2 | 74107185 | |||||
chr2:74107335
|
G | A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(19): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*5159G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5159 | chr2 | 74107335 | |||||
chr2:74107350
|
C | T | 3 | a0001c0002t0008a0001c0002t0046a0001c0002t0053 | 8 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5174C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5174 | chr2 | 74107350 | |||||
chr2:74107663
|
A | G | 44 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(41): Show | 100 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5487A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 12/12 | 5487 | chr2 | 74107663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73985331
|
G | C | 7 | a0001c0002t0001g0005a0001c0002t0048g0002a0001c0003t0010g0003others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-425+174G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985331 | ||||||
chr2:73985335
|
T | TGGCGGGG others(7): Show |
2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG01099.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-425+181_-425+194d others(16): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 73985335 | |||||
chr2:73985402
|
C | G | 4 | a0001c0001t0005g0249a0001c0006t0001g0251a0001c0006t0005g0248others(1): Show | 4 | HG00642.hp1 HG01175.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-425+245C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985402 | ||||||
chr2:73985494
|
G | C | 1 | a0001c0001t0009g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-425+337G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985494 | ||||||
chr2:73985519
|
G | C | 1 | a0001c0001t0009g0012 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-425+362G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985519 | ||||||
chr2:73985529
|
G | A | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-425+372G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985529 | ||||||
chr2:73985604
|
C | T | 1 | a0001c0006t0001g0251 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-424-376C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985604 | ||||||
chr2:73985644
|
T | TG | 68 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(65): Show | 69 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.-424-336_-424-335i others(3): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985644 | ||||||
chr2:73985710
|
G | T | 2 | a0001c0001t0001g0181a0001c0002t0052g0182 | 2 | HG01099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-424-270G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985710 | ||||||
chr2:73985883
|
C | A | 7 | a0001c0002t0001g0014a0001c0002t0008g0015a0001c0002t0008g0017others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-424-97C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 1/11 | chr2 | 73985883 | ||||||
chr2:73986763
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18747.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.303+57G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73986763 | ||||||
chr2:73986785
|
C | T | 1 | a0001c0001t0006g0247 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.303+79C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73986785 | ||||||
chr2:73986993
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.303+287C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73986993 | ||||||
chr2:73987121
|
G | A | 2 | a0001c0001t0058g0024a0001c0001t0059g0023 | 2 | HG02074.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.303+415G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987121 | ||||||
chr2:73987129
|
G | A | 7 | a0001c0002t0001g0014a0001c0002t0008g0015a0001c0002t0008g0017others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+423G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987129 | ||||||
chr2:73987185
|
C | T | 2 | a0002c0005t0002g0178a0002c0005t0002g0179 | 2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.303+479C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987185 | ||||||
chr2:73987255
|
G | A | 2 | a0001c0001t0051g0025a0007c0023t0001g0026 | 2 | HG03017.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.303+549G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987255 | ||||||
chr2:73987320
|
A | G | 3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+614A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987320 | ||||||
chr2:73987629
|
C | G | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.303+923C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987629 | ||||||
chr2:73987665
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.303+959C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987665 | ||||||
chr2:73987920
|
C | T | 9 | a0001c0001t0003g0241a0001c0002t0013g0236a0001c0002t0015g0238others(6): Show | 9 | HG00735.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+1214C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73987920 | ||||||
chr2:73988441
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02165.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.303+1735T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988441 | ||||||
chr2:73988452
|
C | T | 2 | a0001c0002t0002g0175a0001c0002t0007g0174 | 2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.303+1746C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988452 | ||||||
chr2:73988574
|
C | T | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+1868C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988574 | ||||||
chr2:73988645
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | NA18962.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.303+1939A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988645 | ||||||
chr2:73988850
|
C | G | 56 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(53): Show | 57 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.303+2144C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988850 | ||||||
chr2:73988898
|
G | C | 3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+2192G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988898 | ||||||
chr2:73988914
|
C | CT | 7 | a0001c0002t0046g0169a0001c0002t0062g0187a0001c0007t0010g0171others(4): Show | 7 | HG02647.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+2223dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988914 | |||||
chr2:73988914
|
CTT | C | 65 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(62): Show | 66 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.303+2222_303+2223d others(4): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988914 | |||||
chr2:73988977
|
G | GA | 8 | a0001c0001t0001g0029a0001c0002t0001g0005a0001c0002t0048g0002others(5): Show | 8 | HG02056.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+2283dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988977 | |||||
chr2:73988988
|
A | AG | 3 | a0001c0002t0020g0184a0001c0002t0038g0185a0001c0002t0039g0246 | 3 | HG02257.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.303+2282_303+2283i others(3): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988988 | ||||||
chr2:73988989
|
A | G | 2 | a0001c0002t0001g0183a0001c0002t0060g0245 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.303+2283A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988989 | ||||||
chr2:73988989
|
A | T | 5 | a0001c0002t0020g0184a0001c0002t0038g0185a0001c0002t0039g0246others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+2283A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988989 | ||||||
chr2:73988990
|
G | GTTT | 33 | a0001c0001t0003g0241a0001c0001t0006g0199a0001c0001t0006g0200others(30): Show | 33 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.303+2290_303+2292d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988990 | |||||
chr2:73988990
|
G | GTTTT | 18 | a0001c0001t0003g0225a0001c0001t0006g0231a0001c0001t0063g0221others(15): Show | 19 | HG00423.hp2 HG01175.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.303+2289_303+2292d others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988990 | |||||
chr2:73988990
|
G | T | 7 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+2284G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988990 | ||||||
chr2:73988999
|
G | GT | 31 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150others(28): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+2308dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73988999 | |||||
chr2:73988999
|
G | T | 65 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(62): Show | 66 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.303+2293G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73988999 | ||||||
chr2:73989150
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.303+2444C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989150 | ||||||
chr2:73989215
|
C | T | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303+2509C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989215 | ||||||
chr2:73989290
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.303+2584A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989290 | ||||||
chr2:73989388
|
A | T | 39 | a0001c0001t0003g0225a0001c0001t0006g0199a0001c0001t0006g0200others(36): Show | 39 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.303+2682A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989388 | ||||||
chr2:73989605
|
G | A | 3 | a0001c0002t0012g0188a0001c0002t0012g0189a0006c0012t0027g0190 | 3 | HG01884.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.303+2899G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989605 | ||||||
chr2:73989628
|
T | C | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+2922T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989628 | ||||||
chr2:73989637
|
A | G | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+2931A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989637 | ||||||
chr2:73989640
|
C | G | 3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+2934C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989640 | ||||||
chr2:73989648
|
ACTT | A | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+2945_303+2947d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73989648 | |||||
chr2:73989651
|
T | A | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.303+2945T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989651 | ||||||
chr2:73989870
|
T | C | 2 | a0001c0002t0012g0188a0001c0002t0012g0189 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.303+3164T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989870 | ||||||
chr2:73989937
|
C | T | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+3231C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73989937 | ||||||
chr2:73990156
|
G | T | 19 | a0001c0002t0001g0014a0001c0002t0001g0135a0001c0002t0004g0129others(16): Show | 19 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.303+3450G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990156 | ||||||
chr2:73990214
|
T | TA | 174 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0029others(171): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.303+3523dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73990214 | |||||
chr2:73990372
|
G | A | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.303+3666G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990372 | ||||||
chr2:73990411
|
A | G | 1 | a0001c0002t0002g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.303+3705A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990411 | ||||||
chr2:73990462
|
C | A | 2 | a0001c0002t0004g0129a0001c0002t0004g0130 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.303+3756C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990462 | ||||||
chr2:73990552
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.303+3846A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990552 | ||||||
chr2:73990729
|
A | G | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+4023A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990729 | ||||||
chr2:73990994
|
A | G | 2 | a0002c0005t0002g0126a0002c0005t0002g0127 | 2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.303+4288A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73990994 | ||||||
chr2:73991166
|
A | ACTC | 228 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(225): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.303+4462_303+4463i others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73991166 | |||||
chr2:73991167
|
C | CTCT | 3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+4462_303+4463i others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73991167 | |||||
chr2:73991180
|
A | G | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.303+4474A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991180 | ||||||
chr2:73991207
|
G | A | 1 | a0001c0001t0009g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.303+4501G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991207 | ||||||
chr2:73991443
|
C | G | 1 | a0001c0001t0005g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.303+4737C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991443 | ||||||
chr2:73991549
|
T | C | 1 | a0001c0002t0008g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.303+4843T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991549 | ||||||
chr2:73991552
|
T | G | 7 | a0001c0001t0037g0078a0001c0002t0001g0079a0001c0002t0001g0080others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+4846T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991552 | ||||||
chr2:73991683
|
G | A | 1 | a0001c0001t0004g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.303+4977G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991683 | ||||||
chr2:73991762
|
G | A | 1 | a0001c0001t0001g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.303+5056G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991762 | ||||||
chr2:73991805
|
C | CAA | 64 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(61): Show | 65 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.303+5121_303+5122d others(4): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73991805 | |||||
chr2:73991805
|
C | CAAA | 21 | a0001c0001t0003g0241a0001c0001t0006g0247a0001c0001t0021g0191others(18): Show | 21 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.303+5120_303+5122d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73991805 | |||||
chr2:73991805
|
CA | C | 76 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0075others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.303+5122delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73991805 | |||||
chr2:73991978
|
G | C | 1 | a0001c0002t0003g0198 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.303+5272G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73991978 | ||||||
chr2:73992172
|
G | A | 3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+5466G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992172 | ||||||
chr2:73992179
|
T | G | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+5473T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992179 | ||||||
chr2:73992301
|
T | TTTTCTTT others(6): Show |
3 | a0001c0002t0039g0246a0001c0002t0060g0245a0004c0022t0049g0177 | 3 | HG02258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+5607_303+5608i others(15): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73992301 | |||||
chr2:73992301
|
T | TTTTCTTT others(17): Show |
74 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(71): Show | 75 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.303+5609_303+5610i others(26): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73992301 | |||||
chr2:73992301
|
T | TTTTCTTT others(18): Show |
9 | a0001c0001t0006g0219a0001c0001t0006g0231a0001c0001t0006g0247others(6): Show | 9 | HG00423.hp2 HG01106.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+5610_303+5611i others(27): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73992301 | |||||
chr2:73992305
|
C | CT | 6 | a0001c0001t0001g0068a0001c0001t0001g0161a0001c0001t0004g0069others(3): Show | 6 | HG00140.hp1 HG01346.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+5611dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73992305 | |||||
chr2:73992345
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.303+5639G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992345 | ||||||
chr2:73992392
|
C | T | 1 | a0001c0021t0005g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.303+5686C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992392 | ||||||
chr2:73992488
|
T | A | 62 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(59): Show | 63 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.303+5782T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992488 | ||||||
chr2:73992617
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.303+5911G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992617 | ||||||
chr2:73992738
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.303+6032A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992738 | ||||||
chr2:73992759
|
G | C | 5 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(2): Show | 5 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+6053G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992759 | ||||||
chr2:73992821
|
T | C | 59 | a0001c0001t0003g0225a0001c0001t0003g0241a0001c0001t0006g0199others(56): Show | 60 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.303+6115T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992821 | ||||||
chr2:73992908
|
G | A | 5 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(2): Show | 5 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+6202G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73992908 | ||||||
chr2:73993274
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.303+6568G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73993274 | ||||||
chr2:73993395
|
G | C | 1 | a0001c0002t0036g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.303+6689G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73993395 | ||||||
chr2:73993401
|
T | C | 1 | a0001c0002t0004g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.303+6695T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73993401 | ||||||
chr2:73993621
|
G | A | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.303+6915G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73993621 | ||||||
chr2:73993840
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.303+7134C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73993840 | ||||||
chr2:73994299
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.303+7593C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73994299 | ||||||
chr2:73994614
|
TTTTCTTT others(1): Show |
T | 9 | a0001c0002t0001g0014a0001c0002t0003g0207a0001c0002t0003g0208others(6): Show | 9 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+7928_303+7935d others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994614 | |||||
chr2:73994615
|
TTTCTTTC | T | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+7912_303+7918d others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994615 | |||||
chr2:73994631
|
TTTCTTTC | T | 54 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0082others(51): Show | 55 | HG00558.hp2 HG00735.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.303+7928_303+7934d others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994631 | |||||
chr2:73994638
|
C | CT | 12 | a0001c0001t0001g0066a0001c0001t0001g0081a0001c0001t0001g0165others(9): Show | 12 | HG00423.hp1 HG00423.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+7950dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994638 | |||||
chr2:73994638
|
C | CTTTCT | 6 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0012g0188others(3): Show | 6 | HG01099.hp1 HG01884.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+7935_303+7936i others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994638 | |||||
chr2:73994638
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+7932C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73994638 | ||||||
chr2:73994638
|
CT | C | 5 | a0001c0001t0001g0163a0001c0001t0002g0146a0001c0002t0018g0137others(2): Show | 5 | HG01169.hp2 HG01515.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+7950delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994638 | |||||
chr2:73994639
|
T | TTTCTTTC others(4): Show |
2 | a0001c0002t0020g0184a0001c0002t0038g0185 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.303+7935_303+7936i others(13): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994639 | |||||
chr2:73994639
|
T | TTTCTTTC others(8): Show |
1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.303+7935_303+7936i others(17): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73994639 | |||||
chr2:73994661
|
C | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.303+7955C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73994661 | ||||||
chr2:73994793
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+8087G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73994793 | ||||||
chr2:73994829
|
G | T | 2 | a0001c0001t0001g0064a0001c0002t0005g0065 | 2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.303+8123G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73994829 | ||||||
chr2:73995117
|
G | A | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.304-7993G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995117 | ||||||
chr2:73995251
|
T | C | 2 | a0001c0002t0039g0246a0001c0002t0062g0187 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.304-7859T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995251 | ||||||
chr2:73995438
|
T | C | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-7672T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995438 | ||||||
chr2:73995610
|
C | G | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-7500C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995610 | ||||||
chr2:73995664
|
T | G | 1 | a0002c0005t0002g0127 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.304-7446T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995664 | ||||||
chr2:73995732
|
C | A | 18 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(15): Show | 18 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.304-7378C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995732 | ||||||
chr2:73995817
|
C | G | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-7293C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995817 | ||||||
chr2:73995849
|
G | A | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-7261G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995849 | ||||||
chr2:73995930
|
C | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-7180C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73995930 | ||||||
chr2:73996217
|
T | C | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.304-6893T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996217 | ||||||
chr2:73996324
|
T | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(18): Show | 21 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.304-6786T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996324 | ||||||
chr2:73996491
|
T | A | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.304-6619T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996491 | ||||||
chr2:73996639
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-6471C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996639 | ||||||
chr2:73996710
|
G | A | 1 | a0001c0009t0034g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.304-6400G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996710 | ||||||
chr2:73996722
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-6388G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996722 | ||||||
chr2:73996723
|
G | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-6387G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996723 | ||||||
chr2:73996848
|
G | C | 7 | a0001c0002t0001g0014a0001c0002t0008g0015a0001c0002t0008g0017others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-6262G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73996848 | ||||||
chr2:73997016
|
T | C | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-6094T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997016 | ||||||
chr2:73997148
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.304-5962A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997148 | ||||||
chr2:73997351
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(5): Show | 8 | HG01071.hp1 HG01081.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-5759C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997351 | ||||||
chr2:73997372
|
G | A | 2 | a0001c0002t0046g0169a0001c0013t0054g0170 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304-5738G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997372 | ||||||
chr2:73997429
|
C | T | 1 | a0001c0002t0014g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-5681C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997429 | ||||||
chr2:73997436
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-5674C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997436 | ||||||
chr2:73997570
|
A | G | 8 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(5): Show | 9 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-5540A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997570 | ||||||
chr2:73997598
|
A | T | 10 | a0001c0002t0001g0005a0001c0002t0001g0183a0001c0002t0020g0184others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-5512A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997598 | ||||||
chr2:73997704
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-5406C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997704 | ||||||
chr2:73997737
|
G | A | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.304-5373G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997737 | ||||||
chr2:73997834
|
G | C | 4 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0056g0090others(1): Show | 4 | HG01884.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-5276G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997834 | ||||||
chr2:73997835
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.304-5275G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997835 | ||||||
chr2:73997891
|
G | T | 1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304-5219G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997891 | ||||||
chr2:73997904
|
C | T | 1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304-5206C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73997904 | ||||||
chr2:73998051
|
A | C | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-5059A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998051 | ||||||
chr2:73998074
|
A | C | 1 | a0001c0001t0003g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-5036A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998074 | ||||||
chr2:73998137
|
C | T | 29 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(26): Show | 29 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.304-4973C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998137 | ||||||
chr2:73998180
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-4930C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998180 | ||||||
chr2:73998307
|
C | T | 29 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(26): Show | 29 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.304-4803C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998307 | ||||||
chr2:73998457
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-4653C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998457 | ||||||
chr2:73998621
|
A | G | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-4489A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998621 | ||||||
chr2:73998962
|
A | T | 1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304-4148A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998962 | ||||||
chr2:73998975
|
C | T | 98 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(95): Show | 99 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.304-4135C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73998975 | ||||||
chr2:73999014
|
C | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-4096C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73999014 | ||||||
chr2:73999367
|
G | C | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-3743G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73999367 | ||||||
chr2:73999629
|
CCTG | C | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-3477_304-3475d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 73999629 | |||||
chr2:73999789
|
G | A | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.304-3321G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73999789 | ||||||
chr2:73999945
|
C | T | 1 | a0001c0001t0009g0104 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.304-3165C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 73999945 | ||||||
chr2:74000273
|
T | C | 2 | a0001c0002t0046g0169a0001c0013t0054g0170 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304-2837T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000273 | ||||||
chr2:74000361
|
C | T | 46 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0060others(43): Show | 46 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.304-2749C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000361 | ||||||
chr2:74000658
|
G | C | 1 | a0001c0020t0007g0147 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.304-2452G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000658 | ||||||
chr2:74000773
|
C | T | 1 | a0001c0001t0047g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.304-2337C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000773 | ||||||
chr2:74000778
|
C | T | 1 | a0001c0002t0056g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.304-2332C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000778 | ||||||
chr2:74000785
|
C | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-2325C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74000785 | ||||||
chr2:74001073
|
T | C | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-2037T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001073 | ||||||
chr2:74001097
|
C | T | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-2013C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001097 | ||||||
chr2:74001114
|
T | C | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(21): Show | 24 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.304-1996T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001114 | ||||||
chr2:74001338
|
C | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-1772C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001338 | ||||||
chr2:74001526
|
A | G | 1 | a0001c0001t0006g0231 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.304-1584A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001526 | ||||||
chr2:74001624
|
G | C | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.304-1486G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001624 | ||||||
chr2:74001730
|
C | G | 1 | a0001c0001t0002g0157 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.304-1380C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001730 | ||||||
chr2:74001742
|
C | T | 1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.304-1368C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001742 | ||||||
chr2:74001963
|
G | A | 2 | a0001c0002t0039g0246a0001c0002t0042g0013 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.304-1147G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74001963 | ||||||
chr2:74002190
|
A | G | 2 | a0001c0001t0021g0191a0001c0001t0021g0192 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.304-920A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002190 | ||||||
chr2:74002223
|
A | G | 1 | a0001c0001t0006g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.304-887A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002223 | ||||||
chr2:74002272
|
C | T | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.304-838C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002272 | ||||||
chr2:74002395
|
C | A | 1 | a0001c0002t0003g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.304-715C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002395 | ||||||
chr2:74002461
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.304-649T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002461 | ||||||
chr2:74002838
|
C | T | 4 | a0001c0002t0008g0086a0001c0003t0017g0106a0001c0007t0010g0171others(1): Show | 4 | HG01261.hp2 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-272C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002838 | ||||||
chr2:74002848
|
G | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-262G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 2/11 | chr2 | 74002848 | ||||||
chr2:74003183
|
CGTGCGTG others(3): Show |
C | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+31_360+40delCG others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003183 | |||||
chr2:74003424
|
G | GT | 6 | a0001c0001t0001g0037a0001c0001t0001g0180a0001c0001t0006g0201others(3): Show | 6 | HG00738.hp2 HG01257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+274dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003424 | |||||
chr2:74003424
|
G | GTT | 43 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(40): Show | 44 | HG00558.hp2 HG01070.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.360+273_360+274dup others(2): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003424 | |||||
chr2:74003424
|
G | GTTT | 9 | a0001c0002t0001g0014a0001c0002t0003g0230a0001c0002t0008g0017others(6): Show | 9 | HG00735.hp2 HG01169.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+272_360+274dup others(3): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003424 | |||||
chr2:74003424
|
GT | G | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0040others(18): Show | 21 | HG00438.hp2 HG00673.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.360+274delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003424 | |||||
chr2:74003427
|
T | G | 1 | a0001c0004t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+261T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003427 | ||||||
chr2:74003490
|
C | T | 1 | a0001c0004t0002g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.360+324C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003490 | ||||||
chr2:74003529
|
C | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(12): Show | 15 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+363C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003529 | ||||||
chr2:74003559
|
AG | A | 7 | a0001c0002t0001g0005a0001c0002t0048g0002a0001c0003t0010g0003others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+400delG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74003559 | |||||
chr2:74003719
|
A | C | 1 | a0001c0003t0029g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.360+553A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003719 | ||||||
chr2:74003829
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.360+663G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003829 | ||||||
chr2:74003861
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.360+695G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003861 | ||||||
chr2:74003923
|
A | G | 1 | a0001c0007t0033g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.360+757A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74003923 | ||||||
chr2:74004122
|
G | A | 1 | a0001c0001t0019g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.360+956G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004122 | ||||||
chr2:74004194
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(5): Show | 8 | HG01071.hp1 HG01081.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+1028C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004194 | ||||||
chr2:74004761
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0103a0001c0001t0032g0058 | 3 | NA18950.hp2 NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.360+1595A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004761 | ||||||
chr2:74004823
|
G | A | 2 | a0001c0002t0012g0188a0001c0002t0012g0189 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.360+1657G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004823 | ||||||
chr2:74004829
|
C | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.360+1663C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004829 | ||||||
chr2:74004939
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+1773C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74004939 | ||||||
chr2:74005075
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.360+1909C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005075 | ||||||
chr2:74005124
|
T | C | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(13): Show | 16 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+1958T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005124 | ||||||
chr2:74005144
|
G | A | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(13): Show | 16 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+1978G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005144 | ||||||
chr2:74005171
|
A | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(36): Show | 39 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.360+2005A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005171 | ||||||
chr2:74005183
|
T | C | 1 | a0001c0001t0007g0120 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.360+2017T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005183 | ||||||
chr2:74005215
|
G | A | 42 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(39): Show | 42 | HG01071.hp1 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.360+2049G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005215 | ||||||
chr2:74005604
|
G | C | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(13): Show | 16 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+2438G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005604 | ||||||
chr2:74005623
|
G | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0066others(4): Show | 7 | HG00423.hp1 HG00609.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+2457G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005623 | ||||||
chr2:74005641
|
G | A | 4 | a0001c0002t0005g0140a0001c0002t0018g0137a0001c0002t0018g0139others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+2475G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005641 | ||||||
chr2:74005687
|
T | C | 1 | a0001c0017t0001g0031 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.360+2521T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005687 | ||||||
chr2:74005851
|
G | A | 1 | a0001c0002t0004g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.360+2685G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005851 | ||||||
chr2:74005894
|
A | G | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.360+2728A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74005894 | ||||||
chr2:74006084
|
CA | C | 99 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(96): Show | 100 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.360+2928delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74006084 | |||||
chr2:74006156
|
C | G | 7 | a0001c0002t0001g0183a0001c0002t0019g0186a0001c0002t0020g0184others(4): Show | 7 | HG01192.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+2990C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74006156 | ||||||
chr2:74006269
|
T | A | 1 | a0001c0008t0002g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.360+3103T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74006269 | ||||||
chr2:74006363
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.360+3197C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74006363 | ||||||
chr2:74007023
|
A | G | 16 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0183others(13): Show | 16 | HG01099.hp1 HG01192.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+3857A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007023 | ||||||
chr2:74007093
|
A | C | 1 | a0001c0001t0002g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.360+3927A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007093 | ||||||
chr2:74007114
|
A | G | 13 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0012g0188others(10): Show | 13 | HG01099.hp1 HG01192.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+3948A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007114 | ||||||
chr2:74007371
|
G | A | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG01099.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.360+4205G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007371 | ||||||
chr2:74007459
|
A | G | 12 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0012g0188others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.360+4293A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007459 | ||||||
chr2:74007461
|
A | G | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(13): Show | 16 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+4295A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007461 | ||||||
chr2:74007858
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.360+4692G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74007858 | ||||||
chr2:74008039
|
T | C | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+4873T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008039 | ||||||
chr2:74008142
|
A | C | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.360+4976A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008142 | ||||||
chr2:74008181
|
C | G | 5 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(2): Show | 5 | HG02055.hp2 HG02280.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+5015C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008181 | ||||||
chr2:74008389
|
C | G | 2 | a0001c0001t0005g0125a0001c0001t0022g0063 | 2 | HG00621.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.360+5223C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008389 | ||||||
chr2:74008429
|
C | T | 88 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0081others(85): Show | 89 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.360+5263C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008429 | ||||||
chr2:74008664
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0009g0104 | 3 | HG02165.hp1 NA18943.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.360+5498A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008664 | ||||||
chr2:74008712
|
G | T | 54 | a0001c0001t0004g0096a0001c0001t0020g0095a0001c0001t0021g0191others(51): Show | 55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.360+5546G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008712 | ||||||
chr2:74008799
|
A | G | 8 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0002t0001g0135others(5): Show | 8 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+5633A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74008799 | ||||||
chr2:74009064
|
CCT | C | 2 | a0001c0002t0014g0001a0001c0002t0014g0223 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+5901_360+5902d others(4): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74009064 | |||||
chr2:74009067
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.360+5901C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74009067 | ||||||
chr2:74009081
|
G | A | 1 | a0001c0001t0009g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.360+5915G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74009081 | ||||||
chr2:74009288
|
CAG | C | 31 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0002t0001g0005others(28): Show | 32 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.360+6129_360+6130d others(4): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74009288 | |||||
chr2:74009587
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+6421T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74009587 | ||||||
chr2:74009813
|
C | T | 1 | a0001c0008t0002g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.360+6647C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74009813 | ||||||
chr2:74010068
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.360+6902C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010068 | ||||||
chr2:74010105
|
G | T | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+6939G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010105 | ||||||
chr2:74010134
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.360+6968T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010134 | ||||||
chr2:74010301
|
G | C | 1 | a0001c0001t0004g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.360+7135G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010301 | ||||||
chr2:74010394
|
A | G | 1 | a0001c0001t0004g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.360+7228A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010394 | ||||||
chr2:74010445
|
A | G | 2 | a0001c0003t0050g0131a0003c0025t0030g0036 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.360+7279A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010445 | ||||||
chr2:74010549
|
A | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+7383A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010549 | ||||||
chr2:74010754
|
A | C | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+7588A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010754 | ||||||
chr2:74010771
|
T | A | 120 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0004g0041others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.360+7605T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74010771 | ||||||
chr2:74011206
|
C | T | 7 | a0001c0002t0003g0208a0001c0002t0003g0209a0001c0002t0003g0215others(4): Show | 7 | HG01070.hp1 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+8040C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011206 | ||||||
chr2:74011227
|
C | CA | 10 | a0001c0001t0001g0043a0001c0001t0003g0225a0001c0001t0006g0201others(7): Show | 10 | HG00735.hp1 HG00741.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.360+8080dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74011227 | |||||
chr2:74011227
|
C | CAA | 87 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0004g0041others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.360+8079_360+8080d others(4): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74011227 | |||||
chr2:74011227
|
C | CAAA | 22 | a0001c0002t0001g0085a0001c0002t0001g0183a0001c0002t0003g0197others(19): Show | 22 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.360+8078_360+8080d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74011227 | |||||
chr2:74011227
|
CAAAAAAA | C | 5 | a0001c0001t0007g0067a0001c0002t0001g0005a0001c0004t0002g0006others(2): Show | 5 | HG00609.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+8074_360+8080d others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74011227 | |||||
chr2:74011310
|
T | A | 1 | a0001c0002t0004g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.360+8144T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011310 | ||||||
chr2:74011339
|
A | C | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+8173A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011339 | ||||||
chr2:74011353
|
A | G | 2 | a0001c0001t0020g0095a0001c0002t0017g0094 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.360+8187A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011353 | ||||||
chr2:74011422
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0059others(2): Show | 5 | HG02165.hp2 NA18975.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+8256A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011422 | ||||||
chr2:74011554
|
A | G | 121 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0004g0041others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.360+8388A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011554 | ||||||
chr2:74011574
|
G | A | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+8408G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011574 | ||||||
chr2:74011582
|
C | T | 100 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0004g0041others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.360+8416C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011582 | ||||||
chr2:74011583
|
C | T | 1 | a0001c0004t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+8417C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011583 | ||||||
chr2:74011617
|
T | C | 1 | a0001c0001t0005g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.360+8451T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011617 | ||||||
chr2:74011628
|
G | T | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+8462G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011628 | ||||||
chr2:74011730
|
T | C | 6 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+8564T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011730 | ||||||
chr2:74011912
|
A | C | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360+8746A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74011912 | ||||||
chr2:74012073
|
G | C | 8 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0039g0246others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+8907G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012073 | ||||||
chr2:74012388
|
G | A | 63 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0020g0095others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.360+9222G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012388 | ||||||
chr2:74012459
|
T | C | 61 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0004g0041others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.360+9293T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012459 | ||||||
chr2:74012657
|
G | A | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+9491G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012657 | ||||||
chr2:74012833
|
TGAA | T | 10 | a0001c0002t0001g0014a0001c0002t0008g0015a0001c0002t0008g0017others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+9671_360+9673d others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74012833 | |||||
chr2:74012886
|
G | T | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.360+9720G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012886 | ||||||
chr2:74012940
|
T | C | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+9774T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012940 | ||||||
chr2:74012994
|
G | T | 1 | a0001c0002t0016g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.360+9828G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74012994 | ||||||
chr2:74012997
|
G | GT | 33 | a0001c0001t0002g0156a0001c0001t0004g0076a0001c0001t0019g0119others(30): Show | 33 | HG00558.hp2 HG01070.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.360+9847dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74012997 | |||||
chr2:74012997
|
GT | G | 22 | a0001c0001t0001g0027a0001c0002t0001g0005a0001c0002t0001g0135others(19): Show | 22 | HG01106.hp2 HG01433.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.360+9847delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74012997 | |||||
chr2:74013048
|
G | T | 57 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0098others(54): Show | 57 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.360+9882G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013048 | ||||||
chr2:74013231
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.360+10065T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013231 | ||||||
chr2:74013249
|
C | T | 2 | a0001c0002t0002g0093a0001c0002t0002g0128 | 2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.360+10083C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013249 | ||||||
chr2:74013263
|
G | A | 2 | a0001c0002t0011g0206a0003c0025t0030g0036 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.360+10097G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013263 | ||||||
chr2:74013297
|
TG | T | 6 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0046g0169others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+10135delG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74013297 | |||||
chr2:74013408
|
G | A | 1 | a0001c0002t0016g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.360+10242G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013408 | ||||||
chr2:74013510
|
C | T | 101 | a0001c0001t0020g0095a0001c0002t0001g0005a0001c0002t0001g0009others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.360+10344C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013510 | ||||||
chr2:74013513
|
T | C | 8 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0039g0246others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+10347T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013513 | ||||||
chr2:74013668
|
C | T | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.360+10502C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013668 | ||||||
chr2:74013798
|
C | T | 39 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0003g0194others(36): Show | 39 | HG00558.hp2 HG01070.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.360+10632C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013798 | ||||||
chr2:74013910
|
A | G | 118 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.360+10744A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74013910 | ||||||
chr2:74014001
|
G | A | 48 | a0001c0001t0020g0095a0001c0002t0001g0005a0001c0002t0001g0014others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.360+10835G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74014001 | ||||||
chr2:74014518
|
A | G | 11 | a0001c0002t0001g0014a0001c0002t0008g0015a0001c0002t0008g0017others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.360+11352A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74014518 | ||||||
chr2:74014588
|
A | G | 1 | a0002c0005t0002g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.360+11422A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74014588 | ||||||
chr2:74014754
|
C | T | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.360+11588C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74014754 | ||||||
chr2:74014938
|
C | T | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+11772C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74014938 | ||||||
chr2:74015042
|
G | A | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+11876G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015042 | ||||||
chr2:74015119
|
G | T | 2 | a0001c0002t0011g0222a0005c0011t0011g0235 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.360+11953G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015119 | ||||||
chr2:74015123
|
G | A | 1 | a0001c0002t0002g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.360+11957G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015123 | ||||||
chr2:74015174
|
A | T | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.360+12008A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015174 | ||||||
chr2:74015213
|
G | C | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+12047G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015213 | ||||||
chr2:74015724
|
G | A | 2 | a0001c0002t0018g0137a0001c0002t0018g0139 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.360+12558G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015724 | ||||||
chr2:74015740
|
T | C | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360+12574T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015740 | ||||||
chr2:74015776
|
C | T | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.360+12610C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015776 | ||||||
chr2:74015864
|
T | G | 5 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0046g0169others(2): Show | 5 | HG01884.hp2 HG02896.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+12698T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015864 | ||||||
chr2:74015907
|
A | G | 113 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0005others(110): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.360+12741A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015907 | ||||||
chr2:74015961
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+12795T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74015961 | ||||||
chr2:74016043
|
T | C | 13 | a0001c0002t0001g0183a0001c0002t0011g0206a0001c0002t0012g0188others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+12877T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016043 | ||||||
chr2:74016131
|
G | A | 24 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0079others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.360+12965G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016131 | ||||||
chr2:74016210
|
A | G | 13 | a0001c0002t0001g0183a0001c0002t0011g0206a0001c0002t0012g0188others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+13044A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016210 | ||||||
chr2:74016253
|
C | T | 118 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.360+13087C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016253 | ||||||
chr2:74016305
|
TA | T | 7 | a0001c0001t0001g0068a0001c0001t0002g0141a0001c0001t0004g0055others(4): Show | 7 | HG01070.hp2 HG01884.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+13155delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74016305 | |||||
chr2:74016326
|
A | G | 100 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0005others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.360+13160A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016326 | ||||||
chr2:74016469
|
A | C | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+13303A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016469 | ||||||
chr2:74016538
|
A | G | 27 | a0001c0001t0002g0101a0001c0001t0002g0115a0001c0001t0002g0116others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.360+13372A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016538 | ||||||
chr2:74016592
|
C | T | 2 | a0002c0005t0002g0126a0002c0005t0002g0127 | 2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.360+13426C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016592 | ||||||
chr2:74016739
|
C | CA | 100 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0005others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.360+13580dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74016739 | |||||
chr2:74016788
|
C | CT | 63 | a0001c0001t0001g0083a0001c0001t0001g0158a0001c0001t0002g0146others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.360+13639dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74016788 | |||||
chr2:74016788
|
C | CTT | 11 | a0001c0002t0001g0183a0001c0002t0011g0206a0001c0002t0012g0188others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.360+13638_360+1363 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74016788 | |||||
chr2:74016788
|
C | CTTT | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+13637_360+1363 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74016788 | |||||
chr2:74016910
|
A | C | 100 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0005others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.360+13744A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016910 | ||||||
chr2:74016997
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.360+13831T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74016997 | ||||||
chr2:74017074
|
T | C | 19 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.360+13908T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017074 | ||||||
chr2:74017120
|
G | T | 1 | a0001c0001t0004g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.360+13954G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017120 | ||||||
chr2:74017375
|
T | G | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+14209T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017375 | ||||||
chr2:74017489
|
G | A | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+14323G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017489 | ||||||
chr2:74017617
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0019t0004g0035 | 3 | HG03834.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.360+14451G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017617 | ||||||
chr2:74017618
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+14452T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017618 | ||||||
chr2:74017734
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.360+14568A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017734 | ||||||
chr2:74017857
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.360+14691C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017857 | ||||||
chr2:74017863
|
G | A | 6 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+14697G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74017863 | ||||||
chr2:74017961
|
C | CT | 5 | a0001c0001t0001g0037a0001c0001t0001g0164a0001c0001t0002g0118others(2): Show | 5 | HG00438.hp2 HG00738.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+14818dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74017961 | |||||
chr2:74017961
|
CT | C | 88 | a0001c0001t0001g0044a0001c0001t0001g0098a0001c0001t0001g0150others(85): Show | 89 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.360+14818delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74017961 | |||||
chr2:74017961
|
CTT | C | 25 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0079others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.360+14817_360+1481 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74017961 | |||||
chr2:74018194
|
C | T | 17 | a0001c0001t0004g0041a0001c0002t0001g0079a0001c0002t0001g0080others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.360+15028C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018194 | ||||||
chr2:74018200
|
C | G | 12 | a0001c0002t0013g0236a0001c0002t0014g0001a0001c0002t0014g0223others(9): Show | 13 | HG00735.hp2 HG02145.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.360+15034C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018200 | ||||||
chr2:74018257
|
G | A | 5 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0046g0169others(2): Show | 5 | HG01884.hp2 HG02896.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+15091G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018257 | ||||||
chr2:74018267
|
T | A | 2 | a0001c0002t0039g0246a0001c0007t0033g0134 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.360+15101T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018267 | ||||||
chr2:74018293
|
CAT | C | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+15129_360+1513 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74018293 | |||||
chr2:74018354
|
A | T | 1 | a0001c0002t0015g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.360+15188A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018354 | ||||||
chr2:74018365
|
G | A | 115 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.360+15199G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018365 | ||||||
chr2:74018385
|
A | G | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+15219A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018385 | ||||||
chr2:74018411
|
C | T | 5 | a0001c0002t0012g0188a0001c0002t0012g0189a0001c0002t0046g0169others(2): Show | 5 | HG01884.hp2 HG02896.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+15245C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018411 | ||||||
chr2:74018595
|
A | G | 1 | a0001c0001t0020g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.360+15429A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018595 | ||||||
chr2:74018627
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0019t0004g0035 | 3 | HG03834.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.360+15461A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018627 | ||||||
chr2:74018650
|
T | C | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+15484T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018650 | ||||||
chr2:74018737
|
C | T | 16 | a0001c0002t0001g0005a0001c0002t0001g0135a0001c0002t0004g0129others(13): Show | 16 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.360+15571C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018737 | ||||||
chr2:74018744
|
C | CT | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+15594dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74018744 | |||||
chr2:74018744
|
CT | C | 88 | a0001c0001t0002g0141a0001c0001t0004g0041a0001c0001t0020g0095others(85): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.360+15594delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74018744 | |||||
chr2:74018808
|
C | T | 59 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.360+15642C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74018808 | ||||||
chr2:74019018
|
G | C | 1 | a0001c0001t0059g0023 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.360+15852G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019018 | ||||||
chr2:74019190
|
G | C | 1 | a0001c0002t0008g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.360+16024G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019190 | ||||||
chr2:74019282
|
A | C | 1 | a0001c0001t0004g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.360+16116A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019282 | ||||||
chr2:74019423
|
G | A | 46 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0197others(43): Show | 47 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.360+16257G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019423 | ||||||
chr2:74019486
|
T | C | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+16320T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019486 | ||||||
chr2:74019775
|
A | G | 17 | a0001c0002t0001g0005a0001c0002t0001g0135a0001c0002t0004g0129others(14): Show | 17 | HG00741.hp1 HG01106.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.360+16609A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019775 | ||||||
chr2:74019797
|
A | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+16631A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019797 | ||||||
chr2:74019841
|
A | G | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+16675A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019841 | ||||||
chr2:74019871
|
C | G | 1 | a0001c0007t0010g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360+16705C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019871 | ||||||
chr2:74019979
|
A | G | 8 | a0001c0002t0001g0005a0001c0002t0048g0002a0001c0003t0010g0003others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+16813A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019979 | ||||||
chr2:74019994
|
G | A | 7 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(4): Show | 7 | HG00741.hp1 HG01106.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+16828G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74019994 | ||||||
chr2:74020181
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.360+17015C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74020181 | ||||||
chr2:74020222
|
T | G | 2 | a0001c0002t0008g0086a0001c0002t0039g0246 | 2 | HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.360+17056T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74020222 | ||||||
chr2:74020310
|
A | G | 9 | a0001c0002t0001g0183a0001c0002t0012g0188a0001c0002t0012g0189others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+17144A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74020310 | ||||||
chr2:74020523
|
C | T | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.360+17357C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74020523 | ||||||
chr2:74020934
|
C | A | 1 | a0001c0002t0013g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.360+17768C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74020934 | ||||||
chr2:74021185
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.360+18019G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021185 | ||||||
chr2:74021324
|
A | C | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+18158A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021324 | ||||||
chr2:74021504
|
A | G | 4 | a0001c0002t0005g0072a0001c0002t0005g0074a0001c0002t0057g0073others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+18338A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021504 | ||||||
chr2:74021671
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.360+18505G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021671 | ||||||
chr2:74021744
|
A | G | 117 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.360+18578A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021744 | ||||||
chr2:74021790
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.360+18624G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74021790 | ||||||
chr2:74022094
|
C | CCTT | 23 | a0001c0001t0004g0041a0001c0002t0001g0005a0001c0002t0001g0079others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.360+18928_360+1892 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022094 | ||||||
chr2:74022094
|
C | CCTTT | 62 | a0001c0001t0020g0095a0001c0002t0001g0085a0001c0002t0001g0135others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.360+18928_360+1892 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022094 | ||||||
chr2:74022094
|
C | CCTTTT | 26 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(23): Show | 26 | HG00673.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.360+18928_360+1892 others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022094 | ||||||
chr2:74022094
|
C | CCTTTTT | 3 | a0001c0002t0008g0086a0001c0002t0008g0109a0001c0015t0043g0136 | 3 | HG00741.hp2 HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.360+18928_360+1892 others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022094 | ||||||
chr2:74022094
|
CT | C | 116 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.360+18951delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74022094 | |||||
chr2:74022332
|
C | T | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.360+19166C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022332 | ||||||
chr2:74022480
|
G | GT | 9 | a0001c0001t0001g0075a0001c0002t0001g0014a0001c0002t0004g0132others(6): Show | 9 | HG00741.hp1 HG01433.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.360+19323dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74022480 | |||||
chr2:74022854
|
G | A | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.360+19688G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022854 | ||||||
chr2:74022889
|
C | G | 1 | a0001c0002t0024g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.360+19723C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74022889 | ||||||
chr2:74023067
|
C | G | 3 | a0001c0002t0002g0087a0001c0002t0002g0175a0001c0002t0007g0174 | 3 | HG00323.hp1 HG01123.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.360+19901C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023067 | ||||||
chr2:74023123
|
C | G | 2 | a0001c0002t0018g0137a0001c0002t0018g0139 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.360+19957C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023123 | ||||||
chr2:74023280
|
C | T | 1 | a0001c0002t0024g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.360+20114C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023280 | ||||||
chr2:74023305
|
C | T | 1 | a0001c0001t0005g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.360+20139C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023305 | ||||||
chr2:74023423
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.360+20257C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023423 | ||||||
chr2:74023472
|
G | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+20306G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023472 | ||||||
chr2:74023498
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0008t0001g0142others(1): Show | 4 | HG02809.hp2 HG03834.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+20332C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023498 | ||||||
chr2:74023531
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.360+20365C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023531 | ||||||
chr2:74023654
|
C | G | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+20488C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023654 | ||||||
chr2:74023757
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.360+20591A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74023757 | ||||||
chr2:74023876
|
GGA | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+20714_360+2071 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74023876 | |||||
chr2:74024147
|
T | C | 7 | a0001c0002t0011g0206a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+20981T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024147 | ||||||
chr2:74024175
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.360+21009G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024175 | ||||||
chr2:74024484
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.360+21318G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024484 | ||||||
chr2:74024579
|
G | A | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.360+21413G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024579 | ||||||
chr2:74024611
|
G | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+21445G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024611 | ||||||
chr2:74024611
|
GA | G | 3 | a0001c0002t0003g0197a0001c0002t0012g0204a0001c0002t0026g0205 | 3 | HG02055.hp1 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.360+21447delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74024611 | |||||
chr2:74024654
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.360+21488G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024654 | ||||||
chr2:74024674
|
C | A | 1 | a0001c0002t0002g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.360+21508C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024674 | ||||||
chr2:74024775
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.361-21503T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74024775 | ||||||
chr2:74025121
|
G | A | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.361-21157G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025121 | ||||||
chr2:74025149
|
G | A | 25 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0117others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-21129G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025149 | ||||||
chr2:74025153
|
G | A | 1 | a0001c0002t0028g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.361-21125G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025153 | ||||||
chr2:74025223
|
C | CA | 25 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0001g0152others(22): Show | 25 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-21037dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74025223 | |||||
chr2:74025223
|
CA | C | 10 | a0001c0001t0005g0054a0001c0002t0013g0236a0001c0002t0015g0238others(7): Show | 10 | HG00621.hp2 HG00735.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.361-21037delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74025223 | |||||
chr2:74025255
|
C | G | 111 | a0001c0001t0001g0100a0001c0001t0020g0095a0001c0001t0021g0191others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.361-21023C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025255 | ||||||
chr2:74025296
|
T | G | 15 | a0001c0001t0001g0100a0001c0001t0021g0191a0001c0001t0021g0192others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.361-20982T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025296 | ||||||
chr2:74025530
|
G | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-20748G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025530 | ||||||
chr2:74025658
|
T | C | 67 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(64): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.361-20620T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025658 | ||||||
chr2:74025660
|
A | G | 1 | a0001c0010t0004g0166 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.361-20618A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025660 | ||||||
chr2:74025731
|
G | A | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.361-20547G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025731 | ||||||
chr2:74025897
|
A | G | 1 | a0001c0003t0050g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-20381A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025897 | ||||||
chr2:74025948
|
T | A | 62 | a0001c0001t0001g0100a0001c0001t0020g0095a0001c0001t0021g0191others(59): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.361-20330T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74025948 | ||||||
chr2:74026110
|
G | C | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.361-20168G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026110 | ||||||
chr2:74026199
|
A | G | 18 | a0001c0001t0001g0100a0001c0002t0001g0005a0001c0002t0001g0135others(15): Show | 18 | HG00741.hp1 HG01106.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.361-20079A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026199 | ||||||
chr2:74026237
|
C | G | 1 | a0001c0007t0033g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.361-20041C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026237 | ||||||
chr2:74026238
|
A | T | 2 | a0001c0002t0005g0065a0001c0002t0036g0089 | 2 | HG00673.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.361-20040A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026238 | ||||||
chr2:74026253
|
G | C | 1 | a0001c0001t0051g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.361-20025G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026253 | ||||||
chr2:74026281
|
C | G | 23 | a0001c0001t0020g0095a0001c0002t0001g0079a0001c0002t0001g0080others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.361-19997C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026281 | ||||||
chr2:74026350
|
C | A | 41 | a0001c0001t0001g0100a0001c0001t0020g0095a0001c0002t0001g0005others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.361-19928C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026350 | ||||||
chr2:74026437
|
C | T | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-19841C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026437 | ||||||
chr2:74026591
|
G | T | 61 | a0001c0001t0001g0100a0001c0001t0020g0095a0001c0001t0021g0191others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.361-19687G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026591 | ||||||
chr2:74026657
|
T | G | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-19621T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026657 | ||||||
chr2:74026725
|
C | CT | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-19538dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74026725 | |||||
chr2:74026799
|
ACCCAGGG others(3): Show |
A | 1 | a0001c0002t0046g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.361-19477_361-1946 others(14): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74026799 | |||||
chr2:74026804
|
G | A | 1 | a0001c0007t0033g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.361-19474G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026804 | ||||||
chr2:74026905
|
G | C | 1 | a0001c0002t0026g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.361-19373G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74026905 | ||||||
chr2:74027010
|
C | T | 1 | a0001c0004t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.361-19268C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027010 | ||||||
chr2:74027108
|
C | T | 2 | a0001c0001t0009g0104a0001c0001t0058g0024 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.361-19170C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027108 | ||||||
chr2:74027124
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.361-19154C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027124 | ||||||
chr2:74027210
|
G | C | 3 | a0001c0003t0010g0003a0001c0003t0010g0107a0001c0014t0044g0004 | 3 | HG02145.hp1 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.361-19068G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027210 | ||||||
chr2:74027249
|
T | C | 1 | a0001c0003t0029g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.361-19029T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027249 | ||||||
chr2:74027337
|
C | CT | 69 | a0001c0001t0001g0100a0001c0001t0004g0076a0001c0001t0021g0191others(66): Show | 70 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.361-18925dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74027337 | |||||
chr2:74027337
|
C | CTTT | 21 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0079others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.361-18927_361-1892 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74027337 | |||||
chr2:74027337
|
CT | C | 19 | a0001c0001t0001g0060a0001c0001t0001g0162a0001c0001t0002g0115others(16): Show | 19 | HG00323.hp2 HG00741.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.361-18925delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74027337 | |||||
chr2:74027456
|
T | C | 5 | a0001c0001t0002g0101a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG00438.hp2 HG00673.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-18822T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027456 | ||||||
chr2:74027605
|
A | C | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-18673A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027605 | ||||||
chr2:74027992
|
T | C | 1 | a0001c0001t0005g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.361-18286T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74027992 | ||||||
chr2:74028128
|
T | A | 2 | a0001c0002t0001g0085a0001c0002t0055g0145 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.361-18150T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028128 | ||||||
chr2:74028155
|
T | TA | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-18123_361-1812 others(5): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028155 | ||||||
chr2:74028156
|
T | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-18122T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028156 | ||||||
chr2:74028157
|
T | A | 66 | a0001c0001t0001g0100a0001c0001t0004g0041a0001c0001t0020g0095others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.361-18121T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028157 | ||||||
chr2:74028285
|
G | GT | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0053others(4): Show | 7 | HG01081.hp1 HG01167.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-17983dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74028285 | |||||
chr2:74028384
|
G | C | 2 | a0001c0001t0001g0029a0007c0023t0001g0026 | 2 | HG02056.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.361-17894G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028384 | ||||||
chr2:74028487
|
TGTATATG | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0019t0004g0035 | 3 | HG03834.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.361-17788_361-1778 others(11): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74028487 | |||||
chr2:74028629
|
G | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.361-17649G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028629 | ||||||
chr2:74028844
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.361-17434G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028844 | ||||||
chr2:74028888
|
A | G | 67 | a0001c0001t0001g0100a0001c0001t0004g0041a0001c0001t0020g0095others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.361-17390A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028888 | ||||||
chr2:74028888
|
A | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.361-17390A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74028888 | ||||||
chr2:74029130
|
T | C | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-17148T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029130 | ||||||
chr2:74029162
|
A | G | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.361-17116A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029162 | ||||||
chr2:74029178
|
G | A | 113 | a0001c0001t0001g0100a0001c0001t0004g0041a0001c0001t0020g0095others(110): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.361-17100G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029178 | ||||||
chr2:74029442
|
A | G | 1 | a0001c0002t0001g0010 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.361-16836A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029442 | ||||||
chr2:74029707
|
T | C | 1 | a0001c0003t0050g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-16571T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029707 | ||||||
chr2:74029873
|
A | G | 6 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-16405A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029873 | ||||||
chr2:74029967
|
T | C | 102 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.361-16311T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029967 | ||||||
chr2:74029999
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.361-16279A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74029999 | ||||||
chr2:74030040
|
G | A | 1 | a0001c0004t0002g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.361-16238G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030040 | ||||||
chr2:74030195
|
T | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0176a0001c0001t0004g0096others(2): Show | 5 | HG00642.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-16083T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030195 | ||||||
chr2:74030248
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.361-16030A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030248 | ||||||
chr2:74030372
|
G | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-15906G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030372 | ||||||
chr2:74030745
|
G | T | 1 | a0002c0005t0002g0179 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-15533G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030745 | ||||||
chr2:74030758
|
C | G | 24 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0079others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.361-15520C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030758 | ||||||
chr2:74030922
|
G | C | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.361-15356G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030922 | ||||||
chr2:74030957
|
G | A | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-15321G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030957 | ||||||
chr2:74030986
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.361-15292G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74030986 | ||||||
chr2:74031009
|
T | G | 110 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.361-15269T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031009 | ||||||
chr2:74031038
|
A | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-15240A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031038 | ||||||
chr2:74031042
|
G | C | 1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.361-15236G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031042 | ||||||
chr2:74031402
|
T | G | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.361-14876T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031402 | ||||||
chr2:74031482
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-14796C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031482 | ||||||
chr2:74031787
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-14491A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74031787 | ||||||
chr2:74032062
|
C | T | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361-14216C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032062 | ||||||
chr2:74032123
|
T | C | 1 | a0001c0001t0009g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.361-14155T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032123 | ||||||
chr2:74032309
|
G | A | 1 | a0001c0002t0052g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.361-13969G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032309 | ||||||
chr2:74032312
|
G | T | 1 | a0001c0002t0016g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.361-13966G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032312 | ||||||
chr2:74032438
|
G | T | 1 | a0001c0001t0004g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.361-13840G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032438 | ||||||
chr2:74032451
|
C | CTG | 7 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0006g0202others(4): Show | 7 | HG00438.hp2 HG01433.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-13771_361-1377 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
C | CTGTGTGT others(68): Show |
1 | a0001c0002t0060g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.361-13789_361-1378 others(79): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
C | G | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.361-13827C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032451 | ||||||
chr2:74032451
|
CTG | C | 21 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0043others(18): Show | 21 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.361-13771_361-1377 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
CTGTG | C | 21 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0068others(18): Show | 21 | HG01123.hp2 HG01993.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.361-13773_361-1377 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
CTGTGTG | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0034others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-13775_361-1377 others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
CTGTGTGT others(1): Show |
C | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 19 | HG01070.hp2 HG01099.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.361-13777_361-1377 others(12): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
CTGTGTGT others(3): Show |
C | 10 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0066others(7): Show | 10 | HG00280.hp2 HG00423.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.361-13779_361-1377 others(14): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032451
|
CTGTGTGT others(5): Show |
C | 4 | a0001c0001t0001g0033a0001c0001t0001g0059a0001c0001t0001g0158others(1): Show | 4 | HG01081.hp1 NA18975.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-13781_361-1377 others(16): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032451 | |||||
chr2:74032452
|
T | TGTGTGTG others(62): Show |
1 | a0001c0002t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032452 | |||||
chr2:74032452
|
T | TGTGTGTG others(68): Show |
2 | a0001c0002t0006g0195a0001c0002t0028g0239 | 2 | HG03041.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(79): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032452 | |||||
chr2:74032452
|
T | TGTGTGTG others(70): Show |
1 | a0001c0002t0005g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361-13789_361-1378 others(81): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032452 | |||||
chr2:74032454
|
T | TGTGTGTG others(60): Show |
1 | a0001c0002t0004g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.361-13795_361-1379 others(71): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(59): Show |
1 | a0001c0002t0001g0010 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.361-13791_361-1379 others(70): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(66): Show |
3 | a0001c0002t0003g0214a0001c0002t0006g0232a0001c0003t0050g0131 | 3 | NA18989.hp1 NA18999.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(77): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(62): Show |
1 | a0001c0002t0045g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361-13789_361-1378 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(66): Show |
1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.361-13789_361-1378 others(77): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(70): Show |
1 | a0001c0002t0014g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.361-13789_361-1378 others(81): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032454
|
T | TGTGTGTG others(70): Show |
1 | a0001c0002t0013g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.361-13787_361-1378 others(81): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032454 | |||||
chr2:74032456
|
T | TGTGTGTG others(54): Show |
2 | a0001c0002t0004g0129a0001c0002t0004g0130 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.361-13799_361-1379 others(65): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(64): Show |
1 | a0001c0002t0003g0196 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.361-13793_361-1379 others(75): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(58): Show |
2 | a0001c0002t0001g0009a0001c0002t0008g0017 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(69): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(64): Show |
7 | a0001c0002t0003g0194a0001c0002t0003g0207a0001c0002t0003g0226others(4): Show | 7 | HG02717.hp1 NA18974.hp2 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-13791_361-1379 others(75): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(66): Show |
1 | a0001c0002t0014g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(77): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(60): Show |
5 | a0001c0002t0008g0015a0001c0002t0008g0018a0001c0002t0008g0019others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-13789_361-1378 others(71): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(66): Show |
1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361-13789_361-1378 others(77): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032456
|
T | TGTGTGTG others(62): Show |
1 | a0001c0002t0053g0020 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.361-13787_361-1378 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032456 | |||||
chr2:74032458
|
T | TGTGTGTG others(129): Show |
1 | a0001c0004t0002g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.361-13799_361-1379 others(140): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(56): Show |
2 | a0001c0002t0001g0135a0001c0002t0004g0144 | 2 | HG01106.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.361-13795_361-1379 others(67): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(60): Show |
1 | a0001c0002t0026g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.361-13793_361-1379 others(71): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(62): Show |
9 | a0001c0002t0003g0208a0001c0002t0003g0210a0001c0002t0003g0216others(6): Show | 9 | HG00558.hp2 HG01070.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-13791_361-1379 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(64): Show |
1 | a0001c0002t0016g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.361-13791_361-1379 others(75): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(58): Show |
1 | a0001c0002t0008g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.361-13789_361-1378 others(69): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(64): Show |
4 | a0001c0002t0015g0238a0001c0002t0015g0243a0001c0003t0013g0203others(1): Show | 4 | HG01192.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-13789_361-1378 others(75): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(68): Show |
2 | a0001c0002t0003g0212a0001c0003t0013g0244 | 2 | NA18612.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.361-13785_361-1378 others(79): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032458
|
T | TGTGTGTG others(70): Show |
1 | a0001c0004t0003g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361-13783_361-1378 others(81): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032458 | |||||
chr2:74032460
|
T | TGTGTGTG others(51): Show |
1 | a0001c0004t0002g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.361-13799_361-1379 others(62): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(52): Show |
1 | a0001c0014t0044g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.361-13799_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(54): Show |
1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.361-13797_361-1379 others(65): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(52): Show |
1 | a0001c0002t0052g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.361-13795_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(54): Show |
1 | a0002c0005t0002g0149 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.361-13795_361-1379 others(65): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(58): Show |
2 | a0001c0002t0018g0137a0001c0002t0018g0139 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.361-13793_361-1379 others(69): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(60): Show |
1 | a0001c0002t0003g0198 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(71): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032460
|
T | TGTGTGTG others(62): Show |
1 | a0001c0002t0003g0234 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032460 | |||||
chr2:74032462
|
T | TGTGTGTG others(48): Show |
1 | a0001c0002t0048g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.361-13801_361-1380 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(50): Show |
3 | a0001c0002t0001g0005a0001c0003t0010g0003a0001c0004t0002g0008 | 3 | HG02145.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.361-13799_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(48): Show |
1 | a0001c0002t0001g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.361-13797_361-1379 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(50): Show |
4 | a0001c0002t0001g0079a0001c0002t0005g0072a0001c0002t0005g0074others(1): Show | 4 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-13795_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(52): Show |
1 | a0001c0002t0004g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.361-13795_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(52): Show |
6 | a0001c0001t0020g0095a0001c0001t0021g0191a0001c0001t0021g0192others(3): Show | 6 | HG02055.hp2 HG03516.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-13793_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(56): Show |
1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(67): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(58): Show |
1 | a0001c0002t0006g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.361-13791_361-1379 others(69): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032462
|
T | TGTGTGTG others(66): Show |
1 | a0001c0002t0020g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.361-13783_361-1378 others(77): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032462 | |||||
chr2:74032464
|
T | TGTGTGTG others(46): Show |
1 | a0001c0002t0055g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.361-13797_361-1379 others(57): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(48): Show |
11 | a0001c0001t0004g0041a0001c0002t0001g0080a0001c0002t0002g0093others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-13795_361-1379 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(50): Show |
1 | a0001c0001t0063g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.361-13793_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(50): Show |
1 | a0001c0002t0046g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.361-13793_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(52): Show |
1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.361-13791_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(54): Show |
1 | a0001c0002t0007g0174 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(65): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(52): Show |
1 | a0001c0002t0008g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.361-13789_361-1378 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(62): Show |
1 | a0001c0002t0038g0185 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.361-13783_361-1378 others(73): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032464
|
T | TGTGTGTG others(64): Show |
1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.361-13781_361-1378 others(75): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032464 | |||||
chr2:74032466
|
T | TGTGTGTG others(48): Show |
1 | a0001c0002t0017g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.361-13793_361-1379 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032466 | |||||
chr2:74032466
|
T | TGTGTGTG others(52): Show |
3 | a0001c0002t0003g0197a0001c0002t0012g0204a0006c0012t0027g0190 | 3 | HG02055.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(63): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032466 | |||||
chr2:74032466
|
T | TGTGTGTG others(54): Show |
2 | a0001c0002t0003g0209a0001c0002t0003g0215 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(65): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032466 | |||||
chr2:74032466
|
T | TGTGTGTG others(60): Show |
1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.361-13785_361-1378 others(71): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032466 | |||||
chr2:74032468
|
T | TGTGTGTG others(44): Show |
1 | a0001c0002t0002g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.361-13795_361-1379 others(55): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032468 | |||||
chr2:74032468
|
T | TGTGTGTG others(46): Show |
1 | a0001c0002t0002g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.361-13795_361-1379 others(57): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032468 | |||||
chr2:74032468
|
T | TGTGTGTG others(50): Show |
1 | a0001c0003t0029g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.361-13795_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032468 | |||||
chr2:74032468
|
T | TGTGTGTG others(50): Show |
1 | a0001c0002t0056g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361-13791_361-1379 others(61): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032468 | |||||
chr2:74032470
|
T | TGTGTGTG others(40): Show |
1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361-13799_361-1379 others(51): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032470 | |||||
chr2:74032470
|
T | TGTGTGTG others(42): Show |
1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-13797_361-1379 others(53): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032470 | |||||
chr2:74032470
|
T | TGTGTGTG others(48): Show |
2 | a0001c0002t0012g0188a0001c0002t0012g0189 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.361-13791_361-1379 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74032470 | |||||
chr2:74032767
|
A | T | 119 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.361-13511A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032767 | ||||||
chr2:74032777
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.361-13501C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74032777 | ||||||
chr2:74033026
|
T | G | 61 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.361-13252T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033026 | ||||||
chr2:74033225
|
T | C | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-13053T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033225 | ||||||
chr2:74033532
|
A | G | 8 | a0001c0001t0003g0225a0001c0001t0006g0199a0001c0001t0006g0200others(5): Show | 8 | HG00423.hp2 NA18941.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.361-12746A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033532 | ||||||
chr2:74033588
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.361-12690C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033588 | ||||||
chr2:74033772
|
C | T | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361-12506C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033772 | ||||||
chr2:74033870
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-12408C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033870 | ||||||
chr2:74033871
|
G | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-12407G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033871 | ||||||
chr2:74033973
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0005g0032a0001c0017t0001g0031 | 3 | HG01081.hp1 HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.361-12305G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74033973 | ||||||
chr2:74034050
|
C | T | 1 | a0001c0004t0003g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361-12228C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74034050 | ||||||
chr2:74034195
|
T | A | 2 | a0002c0005t0002g0126a0002c0005t0002g0127 | 2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.361-12083T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74034195 | ||||||
chr2:74034247
|
G | GT | 24 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0002t0001g0079others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.361-12020dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74034247 | |||||
chr2:74034575
|
T | TA | 63 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0034others(60): Show | 63 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.361-11684dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74034575 | |||||
chr2:74034575
|
T | TAA | 10 | a0001c0001t0002g0101a0001c0001t0002g0115a0001c0001t0002g0116others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-11685_361-1168 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74034575 | |||||
chr2:74034575
|
TA | T | 60 | a0001c0001t0020g0095a0001c0002t0001g0009a0001c0002t0001g0010others(57): Show | 61 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.361-11684delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74034575 | |||||
chr2:74034837
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18747.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.361-11441G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74034837 | ||||||
chr2:74034964
|
A | G | 109 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.361-11314A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74034964 | ||||||
chr2:74035021
|
C | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.361-11257C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035021 | ||||||
chr2:74035036
|
C | CA | 104 | a0001c0001t0004g0041a0001c0001t0004g0076a0001c0001t0020g0095others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.361-11226dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74035036 | |||||
chr2:74035036
|
C | CAA | 5 | a0001c0002t0001g0183a0001c0002t0004g0129a0001c0002t0004g0132others(2): Show | 5 | HG01433.hp1 HG01515.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-11227_361-1122 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74035036 | |||||
chr2:74035074
|
C | T | 2 | a0001c0002t0004g0132a0002c0005t0002g0149 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.361-11204C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035074 | ||||||
chr2:74035146
|
G | A | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-11132G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035146 | ||||||
chr2:74035201
|
C | CA | 7 | a0001c0001t0006g0247a0001c0002t0001g0183a0001c0002t0020g0184others(4): Show | 7 | HG00741.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-11057dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74035201 | |||||
chr2:74035201
|
CA | C | 127 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-11057delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74035201 | |||||
chr2:74035226
|
T | C | 109 | a0001c0001t0004g0041a0001c0001t0020g0095a0001c0001t0021g0191others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.361-11052T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035226 | ||||||
chr2:74035233
|
C | T | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-11045C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035233 | ||||||
chr2:74035412
|
C | T | 5 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-10866C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035412 | ||||||
chr2:74035413
|
G | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-10865G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035413 | ||||||
chr2:74035469
|
G | GA | 8 | a0001c0001t0005g0108a0001c0002t0003g0197a0001c0002t0012g0188others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-10798dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74035469 | |||||
chr2:74035728
|
A | G | 1 | a0001c0002t0003g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.361-10550A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035728 | ||||||
chr2:74035927
|
A | G | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-10351A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035927 | ||||||
chr2:74035995
|
C | A | 106 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0020g0095others(103): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.361-10283C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74035995 | ||||||
chr2:74036052
|
G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG01169.hp2 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-10226G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74036052 | ||||||
chr2:74036292
|
A | G | 106 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0020g0095others(103): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.361-9986A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74036292 | ||||||
chr2:74036329
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.361-9949G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74036329 | ||||||
chr2:74036665
|
G | A | 18 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0117others(15): Show | 18 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.361-9613G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74036665 | ||||||
chr2:74036853
|
G | A | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-9425G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74036853 | ||||||
chr2:74037081
|
G | C | 44 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(41): Show | 45 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.361-9197G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74037081 | ||||||
chr2:74037230
|
C | T | 5 | a0001c0001t0007g0067a0001c0001t0007g0114a0001c0001t0007g0122others(2): Show | 5 | HG00609.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-9048C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74037230 | ||||||
chr2:74037500
|
G | T | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.361-8778G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74037500 | ||||||
chr2:74037634
|
A | G | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-8644A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74037634 | ||||||
chr2:74038196
|
T | C | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.361-8082T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038196 | ||||||
chr2:74038284
|
G | A | 1 | a0001c0002t0012g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.361-7994G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038284 | ||||||
chr2:74038332
|
A | G | 8 | a0001c0002t0001g0005a0001c0002t0048g0002a0001c0003t0010g0003others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-7946A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038332 | ||||||
chr2:74038423
|
G | A | 1 | a0001c0007t0010g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.361-7855G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038423 | ||||||
chr2:74038432
|
G | T | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361-7846G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038432 | ||||||
chr2:74038806
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-7472C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038806 | ||||||
chr2:74038976
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0176 | 2 | HG00642.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.361-7302C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74038976 | ||||||
chr2:74039089
|
A | G | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.361-7189A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039089 | ||||||
chr2:74039132
|
A | G | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-7146A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039132 | ||||||
chr2:74039259
|
A | C | 1 | a0001c0002t0028g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.361-7019A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039259 | ||||||
chr2:74039322
|
C | G | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.361-6956C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039322 | ||||||
chr2:74039322
|
C | T | 1 | a0001c0001t0005g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.361-6956C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039322 | ||||||
chr2:74039625
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.361-6653G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039625 | ||||||
chr2:74039651
|
A | G | 59 | a0001c0001t0020g0095a0001c0002t0001g0005a0001c0002t0001g0009others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.361-6627A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039651 | ||||||
chr2:74039872
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.361-6406G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039872 | ||||||
chr2:74039877
|
C | T | 1 | a0001c0002t0020g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.361-6401C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039877 | ||||||
chr2:74039946
|
G | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-6332G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74039946 | ||||||
chr2:74040202
|
A | G | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-6076A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040202 | ||||||
chr2:74040248
|
C | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.361-6030C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040248 | ||||||
chr2:74040393
|
C | G | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-5885C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040393 | ||||||
chr2:74040529
|
C | A | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.361-5749C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040529 | ||||||
chr2:74040763
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.361-5515G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040763 | ||||||
chr2:74040780
|
A | G | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-5498A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74040780 | ||||||
chr2:74041007
|
A | G | 56 | a0001c0001t0020g0095a0001c0002t0001g0005a0001c0002t0001g0009others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.361-5271A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041007 | ||||||
chr2:74041400
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-4878C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041400 | ||||||
chr2:74041401
|
G | A | 1 | a0001c0002t0046g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.361-4877G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041401 | ||||||
chr2:74041432
|
G | T | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-4846G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041432 | ||||||
chr2:74041451
|
A | G | 42 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(39): Show | 43 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.361-4827A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041451 | ||||||
chr2:74041584
|
A | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.361-4694A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041584 | ||||||
chr2:74041652
|
G | A | 1 | a0001c0008t0002g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.361-4626G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041652 | ||||||
chr2:74041975
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.361-4303C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74041975 | ||||||
chr2:74042005
|
A | C | 14 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.361-4273A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042005 | ||||||
chr2:74042152
|
G | A | 55 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(52): Show | 55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.361-4126G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042152 | ||||||
chr2:74042454
|
C | T | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-3824C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042454 | ||||||
chr2:74042654
|
G | A | 1 | a0001c0001t0037g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.361-3624G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042654 | ||||||
chr2:74042709
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-3569C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042709 | ||||||
chr2:74042799
|
T | C | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.361-3479T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042799 | ||||||
chr2:74042869
|
G | A | 1 | a0001c0010t0004g0166 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.361-3409G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042869 | ||||||
chr2:74042871
|
T | A | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-3407T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74042871 | ||||||
chr2:74043174
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18747.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.361-3104G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74043174 | ||||||
chr2:74043206
|
G | C | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-3072G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74043206 | ||||||
chr2:74043327
|
A | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-2951A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74043327 | ||||||
chr2:74043444
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.361-2834G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74043444 | ||||||
chr2:74043907
|
C | T | 1 | a0001c0001t0005g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.361-2371C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74043907 | ||||||
chr2:74044034
|
G | A | 2 | a0001c0002t0015g0238a0001c0002t0015g0243 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.361-2244G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74044034 | ||||||
chr2:74044106
|
G | C | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-2172G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74044106 | ||||||
chr2:74044152
|
G | T | 2 | a0001c0002t0003g0233a0001c0002t0016g0193 | 2 | NA19009.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.361-2126G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74044152 | ||||||
chr2:74044188
|
T | G | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-2090T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74044188 | ||||||
chr2:74044450
|
C | T | 74 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(71): Show | 75 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.361-1828C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74044450 | ||||||
chr2:74045029
|
A | G | 3 | a0001c0003t0010g0003a0001c0003t0010g0107a0001c0014t0044g0004 | 3 | HG02145.hp1 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.361-1249A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045029 | ||||||
chr2:74045038
|
A | G | 2 | a0001c0001t0002g0146a0001c0008t0002g0148 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361-1240A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045038 | ||||||
chr2:74045083
|
G | A | 247 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(244): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.361-1195G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045083 | ||||||
chr2:74045130
|
A | C | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.361-1148A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045130 | ||||||
chr2:74045162
|
A | T | 1 | a0001c0001t0004g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.361-1116A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045162 | ||||||
chr2:74045183
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-1095A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045183 | ||||||
chr2:74045291
|
T | C | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.361-987T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045291 | ||||||
chr2:74045315
|
G | A | 2 | a0001c0008t0001g0142a0003c0025t0030g0036 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.361-963G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045315 | ||||||
chr2:74045456
|
A | G | 2 | a0001c0001t0020g0095a0001c0007t0033g0134 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.361-822A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045456 | ||||||
chr2:74045731
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.361-547A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045731 | ||||||
chr2:74045845
|
C | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-433C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74045845 | ||||||
chr2:74046113
|
A | G | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.361-165A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | chr2 | 74046113 | ||||||
chr2:74046256
|
T | TC | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.361-17dupC | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 74046256 | |||||
chr2:74048601
|
G | A | 1 | a0001c0002t0060g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+190G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74048601 | ||||||
chr2:74048774
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2494+363A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74048774 | ||||||
chr2:74048976
|
A | G | 2 | a0001c0002t0006g0195a0001c0002t0006g0232 | 2 | NA18999.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2494+565A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74048976 | ||||||
chr2:74049019
|
A | C | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2494+608A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74049019 | ||||||
chr2:74049021
|
G | A | 1 | a0001c0002t0038g0185 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2494+610G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74049021 | ||||||
chr2:74049205
|
T | G | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494+794T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74049205 | ||||||
chr2:74049717
|
T | G | 1 | a0001c0001t0006g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2494+1306T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74049717 | ||||||
chr2:74050003
|
C | T | 21 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(18): Show | 21 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.2494+1592C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050003 | ||||||
chr2:74050011
|
C | G | 10 | a0001c0002t0001g0005a0001c0002t0018g0137a0001c0002t0018g0139others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2494+1600C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050011 | ||||||
chr2:74050165
|
A | G | 1 | a0001c0002t0011g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2494+1754A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050165 | ||||||
chr2:74050252
|
C | T | 6 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+1841C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050252 | ||||||
chr2:74050437
|
G | A | 2 | a0001c0002t0003g0197a0001c0002t0012g0204 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2494+2026G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050437 | ||||||
chr2:74050532
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2494+2121T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050532 | ||||||
chr2:74050624
|
A | T | 1 | a0001c0007t0010g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2494+2213A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050624 | ||||||
chr2:74050800
|
T | C | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+2389T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74050800 | ||||||
chr2:74050876
|
AAAC | A | 6 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+2471_2494+247 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74050876 | |||||
chr2:74051215
|
C | G | 1 | a0001c0002t0020g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2494+2804C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051215 | ||||||
chr2:74051239
|
G | A | 1 | a0001c0001t0059g0023 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2494+2828G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051239 | ||||||
chr2:74051294
|
C | T | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2494+2883C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051294 | ||||||
chr2:74051354
|
A | G | 116 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2494+2943A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051354 | ||||||
chr2:74051412
|
A | C | 1 | a0008c0024t0001g0046 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2494+3001A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051412 | ||||||
chr2:74051513
|
G | A | 12 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(9): Show | 12 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2494+3102G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051513 | ||||||
chr2:74051541
|
G | A | 1 | a0001c0002t0004g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2494+3130G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051541 | ||||||
chr2:74051588
|
C | G | 1 | a0001c0001t0004g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2494+3177C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051588 | ||||||
chr2:74051598
|
G | A | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2494+3187G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051598 | ||||||
chr2:74051823
|
A | G | 1 | a0001c0001t0040g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2494+3412A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74051823 | ||||||
chr2:74052014
|
C | G | 2 | a0001c0001t0004g0091a0001c0001t0007g0120 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2494+3603C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052014 | ||||||
chr2:74052099
|
C | T | 1 | a0001c0002t0016g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2494+3688C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052099 | ||||||
chr2:74052338
|
G | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0180 | 3 | HG02738.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2494+3927G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052338 | ||||||
chr2:74052390
|
T | C | 8 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2494+3979T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052390 | ||||||
chr2:74052533
|
A | G | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2494+4122A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052533 | ||||||
chr2:74052556
|
C | CA | 70 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0173others(67): Show | 70 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2494+4165dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74052556 | |||||
chr2:74052556
|
C | CAA | 6 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(3): Show | 6 | HG00735.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+4164_2494+416 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74052556 | |||||
chr2:74052556
|
C | CAAA | 6 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+4163_2494+416 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74052556 | |||||
chr2:74052556
|
CA | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0004g0069others(25): Show | 28 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.2494+4165delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74052556 | |||||
chr2:74052751
|
T | C | 85 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(82): Show | 86 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.2494+4340T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052751 | ||||||
chr2:74052755
|
A | G | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2494+4344A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052755 | ||||||
chr2:74052988
|
G | A | 175 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0068others(172): Show | 176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2494+4577G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74052988 | ||||||
chr2:74053148
|
G | A | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2494+4737G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053148 | ||||||
chr2:74053242
|
G | T | 104 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.2494+4831G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053242 | ||||||
chr2:74053243
|
T | TC | 23 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0085others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.2494+4840dupC | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74053243 | |||||
chr2:74053423
|
T | C | 1 | a0001c0018t0031g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2494+5012T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053423 | ||||||
chr2:74053433
|
G | C | 4 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+5022G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053433 | ||||||
chr2:74053530
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0158 | 3 | HG03834.hp1 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2494+5119C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053530 | ||||||
chr2:74053712
|
G | A | 1 | a0001c0001t0059g0023 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2494+5301G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053712 | ||||||
chr2:74053833
|
C | T | 1 | a0001c0002t0006g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2494+5422C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053833 | ||||||
chr2:74053869
|
A | G | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2494+5458A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053869 | ||||||
chr2:74053905
|
C | T | 1 | a0001c0001t0019g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2494+5494C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74053905 | ||||||
chr2:74054318
|
G | GA | 14 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2494+5909dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74054318 | |||||
chr2:74054714
|
G | C | 7 | a0001c0001t0007g0067a0001c0001t0007g0114a0001c0001t0007g0121others(4): Show | 7 | HG00558.hp1 HG00609.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.2494+6303G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74054714 | ||||||
chr2:74055003
|
G | C | 110 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2494+6592G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74055003 | ||||||
chr2:74055320
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0005g0054 | 2 | HG00621.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2494+6909A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74055320 | ||||||
chr2:74055522
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2494+7111G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74055522 | ||||||
chr2:74055579
|
T | C | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2494+7168T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74055579 | ||||||
chr2:74055905
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2494+7494G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74055905 | ||||||
chr2:74056135
|
C | G | 1 | a0001c0002t0004g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2494+7724C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056135 | ||||||
chr2:74056137
|
G | C | 2 | a0001c0001t0020g0095a0001c0007t0033g0134 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2494+7726G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056137 | ||||||
chr2:74056170
|
G | A | 1 | a0001c0001t0007g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2494+7759G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056170 | ||||||
chr2:74056354
|
T | C | 1 | a0001c0001t0009g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2494+7943T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056354 | ||||||
chr2:74056403
|
A | G | 2 | a0001c0002t0005g0140a0001c0002t0019g0186 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2494+7992A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056403 | ||||||
chr2:74056601
|
C | T | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2494+8190C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056601 | ||||||
chr2:74056616
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2494+8205G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056616 | ||||||
chr2:74056850
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2494+8439A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056850 | ||||||
chr2:74056906
|
G | A | 118 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2494+8495G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74056906 | ||||||
chr2:74057283
|
A | G | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2494+8872A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057283 | ||||||
chr2:74057317
|
A | C | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2494+8906A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057317 | ||||||
chr2:74057559
|
T | C | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2494+9148T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057559 | ||||||
chr2:74057560
|
A | G | 118 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2494+9149A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057560 | ||||||
chr2:74057640
|
T | G | 1 | a0001c0001t0004g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2494+9229T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057640 | ||||||
chr2:74057698
|
C | A | 1 | a0001c0002t0024g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2494+9287C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057698 | ||||||
chr2:74057765
|
C | T | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2494+9354C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057765 | ||||||
chr2:74057958
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2494+9547T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74057958 | ||||||
chr2:74058033
|
C | G | 80 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(77): Show | 81 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.2494+9622C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058033 | ||||||
chr2:74058114
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2494+9703T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058114 | ||||||
chr2:74058434
|
A | G | 1 | a0001c0002t0016g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2494+10023A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058434 | ||||||
chr2:74058524
|
T | TA | 10 | a0001c0001t0001g0150a0001c0002t0003g0197a0001c0002t0011g0206others(7): Show | 10 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2494+10126dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74058524 | |||||
chr2:74058811
|
C | A | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2494+10400C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058811 | ||||||
chr2:74058913
|
T | C | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2494+10502T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058913 | ||||||
chr2:74058926
|
A | G | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2494+10515A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058926 | ||||||
chr2:74058954
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0032g0058 | 2 | NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2494+10543T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058954 | ||||||
chr2:74058963
|
C | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2494+10552C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058963 | ||||||
chr2:74058981
|
T | C | 1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2494+10570T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74058981 | ||||||
chr2:74059316
|
A | T | 1 | a0001c0001t0004g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2494+10905A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74059316 | ||||||
chr2:74059922
|
T | C | 2 | a0001c0001t0009g0104a0001c0001t0058g0024 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2494+11511T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74059922 | ||||||
chr2:74059996
|
T | C | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2494+11585T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74059996 | ||||||
chr2:74060265
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2494+11854G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060265 | ||||||
chr2:74060500
|
C | T | 1 | a0001c0002t0017g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2494+12089C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060500 | ||||||
chr2:74060521
|
T | A | 2 | a0001c0002t0004g0129a0001c0002t0004g0130 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2494+12110T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060521 | ||||||
chr2:74060522
|
A | T | 73 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0158others(70): Show | 74 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.2494+12111A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060522 | ||||||
chr2:74060594
|
G | A | 3 | a0001c0002t0013g0236a0001c0003t0013g0244a0001c0004t0003g0240 | 3 | HG02723.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+12183G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060594 | ||||||
chr2:74060790
|
A | G | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+12379A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060790 | ||||||
chr2:74060808
|
A | G | 3 | a0001c0002t0002g0087a0001c0002t0002g0175a0001c0002t0007g0174 | 3 | HG00323.hp1 HG01123.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.2494+12397A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060808 | ||||||
chr2:74060914
|
C | T | 3 | a0001c0002t0002g0087a0001c0002t0002g0175a0001c0002t0007g0174 | 3 | HG00323.hp1 HG01123.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.2494+12503C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060914 | ||||||
chr2:74060930
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0158 | 2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2494+12519A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060930 | ||||||
chr2:74060978
|
A | G | 2 | a0001c0002t0012g0188a0001c0002t0012g0189 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2494+12567A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74060978 | ||||||
chr2:74061009
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0152a0001c0001t0001g0163others(2): Show | 5 | HG01169.hp2 HG02258.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495-12540C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061009 | ||||||
chr2:74061043
|
C | CG | 4 | a0001c0001t0002g0118a0001c0001t0021g0191a0001c0007t0010g0171others(1): Show | 4 | HG00438.hp2 HG02055.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-12502dupG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061043 | |||||
chr2:74061043
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-12506C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061043 | ||||||
chr2:74061093
|
G | A | 2 | a0001c0001t0002g0099a0007c0023t0001g0026 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2495-12456G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061093 | ||||||
chr2:74061116
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2495-12433C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061116 | ||||||
chr2:74061124
|
GCGGC | G | 18 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0117others(15): Show | 18 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.2495-12417_2495-12 others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061124 | |||||
chr2:74061129
|
C | T | 1 | a0001c0021t0005g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2495-12420C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061129 | ||||||
chr2:74061167
|
G | A | 87 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2495-12382G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061167 | ||||||
chr2:74061179
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2495-12370C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061179 | ||||||
chr2:74061183
|
C | T | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2495-12366C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061183 | ||||||
chr2:74061209
|
C | CCCTCCCG others(347): Show |
1 | a0001c0003t0010g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2495-12330_2495-12 others(360): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061209 | |||||
chr2:74061220
|
G | A | 40 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(37): Show | 40 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2495-12329G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061220 | ||||||
chr2:74061224
|
T | C | 1 | a0001c0003t0010g0003 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2495-12325T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061224 | ||||||
chr2:74061224
|
T | TGGCTGGC others(345): Show |
5 | a0001c0002t0052g0182a0002c0005t0002g0126a0002c0005t0002g0127others(2): Show | 5 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495-12187_2495-12 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061224 | |||||
chr2:74061224
|
T | TGGCTGGC others(345): Show |
32 | a0001c0002t0001g0005a0001c0002t0001g0135a0001c0002t0004g0129others(29): Show | 33 | HG00735.hp2 HG01106.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.2495-12187_2495-12 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061224 | |||||
chr2:74061224
|
T | TGGCTGGC others(697): Show |
1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2495-12187_2495-12 others(710): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061224 | |||||
chr2:74061224
|
T | TGGCTGGC others(346): Show |
1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2495-12187_2495-12 others(359): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061224 | |||||
chr2:74061224
|
T | TGGCTGGC others(346): Show |
3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2495-12187_2495-12 others(359): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061224 | |||||
chr2:74061232
|
C | TGGGCGGG others(345): Show |
2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2495-12318_2495-12 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061232 | ||||||
chr2:74061233
|
G | C | 8 | a0001c0002t0003g0197a0001c0002t0011g0206a0001c0002t0012g0188others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-12316G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061233 | ||||||
chr2:74061336
|
ACCTCCCG others(42): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2495-12190_2495-12 others(55): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061336 | |||||
chr2:74061363
|
T | C | 120 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2495-12186T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061363 | ||||||
chr2:74061373
|
A | ACCCCCCC others(346): Show |
1 | a0002c0005t0002g0179 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2495-12108_2495-12 others(359): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061373 | |||||
chr2:74061374
|
C | CCCCCCCA others(344): Show |
25 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(22): Show | 25 | HG00558.hp2 HG01070.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.2495-11944_2495-11 others(357): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061374 | |||||
chr2:74061374
|
C | CCCCCCCA others(345): Show |
1 | a0001c0002t0003g0230 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2495-12083_2495-12 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061374 | |||||
chr2:74061395
|
C | TGGGGCGG others(344): Show |
2 | a0001c0002t0005g0140a0001c0002t0019g0186 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2495-12155_2495-12 others(357): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061395 | ||||||
chr2:74061395
|
C | TGGGGCGG others(345): Show |
1 | a0001c0002t0006g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2495-12155_2495-12 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061395 | ||||||
chr2:74061418
|
G | A | 1 | a0001c0003t0050g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2495-12131G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061418 | ||||||
chr2:74061434
|
CCCTCCCG others(120): Show |
C | 2 | a0001c0001t0004g0123a0001c0010t0004g0166 | 2 | NA18977.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2495-12092_2495-11 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061434 | |||||
chr2:74061436
|
CTCCCGGA others(42): Show |
C | 1 | a0001c0001t0005g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2495-12092_2495-12 others(55): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061436 | |||||
chr2:74061440
|
C | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495-12109C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061440 | ||||||
chr2:74061457
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2495-12092A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061457 | ||||||
chr2:74061461
|
C | CGGGGGAC others(346): Show |
1 | a0001c0003t0013g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2495-11941_2495-11 others(359): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061461 | |||||
chr2:74061577
|
G | A | 8 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0052g0182others(5): Show | 8 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-11972G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061577 | ||||||
chr2:74061577
|
G | GGCTGGCC others(345): Show |
8 | a0001c0002t0002g0087a0001c0002t0002g0093a0001c0002t0002g0128others(5): Show | 8 | HG00323.hp1 HG00673.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-11944_2495-11 others(358): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061577 | |||||
chr2:74061577
|
G | GGCTGGCC others(346): Show |
1 | a0001c0002t0001g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2495-11944_2495-11 others(359): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061577 | |||||
chr2:74061585
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2495-11964G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061585 | ||||||
chr2:74061588
|
C | A | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0044others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2495-11961C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061588 | ||||||
chr2:74061592
|
G | GGGCTGAC others(27): Show |
1 | a0001c0001t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2495-11951_2495-11 others(40): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061592 | |||||
chr2:74061599
|
C | CCCCCCCA others(343): Show |
1 | a0001c0003t0050g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2495-11944_2495-11 others(356): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061599 | |||||
chr2:74061661
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2495-11888C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061661 | ||||||
chr2:74061667
|
GGCTGCCG others(33): Show |
G | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2495-11842_2495-11 others(46): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061667 | |||||
chr2:74061688
|
C | G | 8 | a0001c0002t0003g0197a0001c0002t0011g0206a0001c0002t0012g0188others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-11861C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061688 | ||||||
chr2:74061701
|
C | T | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-11848C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061701 | ||||||
chr2:74061725
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-11824C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061725 | ||||||
chr2:74061746
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-11803C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061746 | ||||||
chr2:74061794
|
T | C | 3 | a0001c0001t0005g0061a0001c0001t0005g0071a0001c0001t0005g0249 | 3 | HG01175.hp1 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2495-11755T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061794 | ||||||
chr2:74061799
|
GCGCTCCT others(32): Show |
G | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495-11739_2495-11 others(45): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061799 | |||||
chr2:74061806
|
T | TCACATCC others(30): Show |
87 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2495-11737_2495-11 others(43): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74061806 | |||||
chr2:74061871
|
G | A | 2 | a0001c0001t0002g0099a0007c0023t0001g0026 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2495-11678G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061871 | ||||||
chr2:74061910
|
G | A | 2 | a0001c0002t0026g0205a0001c0002t0028g0239 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2495-11639G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061910 | ||||||
chr2:74061961
|
C | T | 2 | a0001c0002t0001g0183a0001c0002t0038g0185 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2495-11588C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061961 | ||||||
chr2:74061982
|
G | A | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-11567G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74061982 | ||||||
chr2:74062063
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2495-11486G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062063 | ||||||
chr2:74062148
|
C | G | 5 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-11401C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062148 | ||||||
chr2:74062149
|
C | G | 5 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-11400C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062149 | ||||||
chr2:74062149
|
C | T | 1 | a0001c0021t0005g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2495-11400C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062149 | ||||||
chr2:74062157
|
G | A | 1 | a0001c0007t0010g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2495-11392G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062157 | ||||||
chr2:74062215
|
T | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0158others(2): Show | 5 | HG02922.hp2 HG03834.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-11334T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062215 | ||||||
chr2:74062609
|
T | C | 1 | a0001c0009t0034g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2495-10940T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74062609 | ||||||
chr2:74062881
|
C | CT | 11 | a0001c0001t0001g0037a0001c0001t0001g0064a0001c0001t0001g0164others(8): Show | 11 | HG00609.hp1 HG01261.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2495-10648dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74062881 | |||||
chr2:74062881
|
C | CTT | 96 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(93): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2495-10649_2495-10 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74062881 | |||||
chr2:74062881
|
C | CTTT | 5 | a0001c0002t0012g0189a0001c0002t0012g0204a0001c0002t0062g0187others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-10650_2495-10 others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74062881 | |||||
chr2:74062881
|
CT | C | 8 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-10648delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74062881 | |||||
chr2:74063189
|
CT | C | 115 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2495-10347delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063189 | |||||
chr2:74063225
|
A | C | 1 | a0001c0001t0047g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2495-10324A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063225 | ||||||
chr2:74063226
|
T | G | 2 | a0001c0007t0010g0171a0003c0025t0030g0036 | 2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2495-10323T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063226 | ||||||
chr2:74063284
|
A | C | 1 | a0002c0005t0002g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2495-10265A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063284 | ||||||
chr2:74063583
|
TTA | T | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-9962_2495-996 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063583 | |||||
chr2:74063606
|
A | G | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-9943A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063606 | ||||||
chr2:74063677
|
A | G | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2495-9872A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063677 | ||||||
chr2:74063888
|
G | A | 110 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2495-9661G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063888 | ||||||
chr2:74063893
|
C | CA | 6 | a0001c0001t0001g0152a0001c0001t0002g0052a0001c0001t0005g0249others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-9640dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063893 | |||||
chr2:74063893
|
C | CAA | 8 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(5): Show | 8 | HG01433.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-9641_2495-964 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063893 | |||||
chr2:74063893
|
C | CAAA | 66 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0085others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2495-9642_2495-964 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063893 | |||||
chr2:74063893
|
C | CAAAA | 37 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(34): Show | 38 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.2495-9643_2495-964 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063893 | |||||
chr2:74063893
|
CA | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0056others(5): Show | 8 | HG00323.hp2 HG02056.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-9640delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063893 | |||||
chr2:74063910
|
T | A | 2 | a0001c0002t0035g0092a0001c0002t0039g0246 | 2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2495-9639T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74063910 | ||||||
chr2:74063976
|
T | TTCTTCAT others(48): Show |
1 | a0001c0013t0054g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2495-9571_2495-951 others(59): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74063976 | |||||
chr2:74064007
|
G | A | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2495-9542G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064007 | ||||||
chr2:74064046
|
T | C | 1 | a0001c0001t0009g0012 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2495-9503T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064046 | ||||||
chr2:74064234
|
G | C | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-9315G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064234 | ||||||
chr2:74064260
|
C | T | 23 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(20): Show | 23 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2495-9289C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064260 | ||||||
chr2:74064363
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2495-9186T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064363 | ||||||
chr2:74064370
|
T | G | 67 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0044others(64): Show | 67 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2495-9179T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064370 | ||||||
chr2:74064384
|
C | G | 1 | a0001c0001t0009g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2495-9165C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064384 | ||||||
chr2:74064470
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-9079A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064470 | ||||||
chr2:74064919
|
G | C | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2495-8630G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74064919 | ||||||
chr2:74065087
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0005g0113 | 2 | HG02040.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2495-8462G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065087 | ||||||
chr2:74065165
|
G | T | 1 | a0001c0004t0002g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2495-8384G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065165 | ||||||
chr2:74065311
|
A | C | 1 | a0001c0001t0005g0071 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2495-8238A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065311 | ||||||
chr2:74065349
|
C | G | 1 | a0001c0002t0019g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2495-8200C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065349 | ||||||
chr2:74065349
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2495-8200C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065349 | ||||||
chr2:74065447
|
C | G | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2495-8102C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065447 | ||||||
chr2:74065555
|
G | GT | 14 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0098others(11): Show | 14 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495-7980dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74065555 | |||||
chr2:74065555
|
G | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-7994G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065555 | ||||||
chr2:74065555
|
GT | G | 74 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(71): Show | 75 | HG00558.hp2 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.2495-7980delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74065555 | |||||
chr2:74065556
|
T | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-7993T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065556 | ||||||
chr2:74065596
|
T | C | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495-7953T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065596 | ||||||
chr2:74065600
|
TTCCGTCC others(1): Show |
T | 2 | a0001c0001t0063g0221a0001c0016t0001g0105 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2495-7933_2495-792 others(12): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74065600 | |||||
chr2:74065620
|
G | GTCCT | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2495-7914_2495-791 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74065620 | |||||
chr2:74065620
|
G | T | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2495-7929G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065620 | ||||||
chr2:74065652
|
T | C | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2495-7897T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065652 | ||||||
chr2:74065658
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2495-7891C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065658 | ||||||
chr2:74065764
|
G | C | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-7785G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065764 | ||||||
chr2:74065845
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2495-7704G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065845 | ||||||
chr2:74065908
|
G | A | 1 | a0001c0004t0025g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2495-7641G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065908 | ||||||
chr2:74065915
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-7634T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065915 | ||||||
chr2:74065961
|
G | C | 1 | a0001c0001t0002g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2495-7588G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065961 | ||||||
chr2:74065962
|
G | T | 109 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2495-7587G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74065962 | ||||||
chr2:74066039
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2495-7510G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066039 | ||||||
chr2:74066147
|
T | A | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2495-7402T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066147 | ||||||
chr2:74066250
|
A | G | 13 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2495-7299A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066250 | ||||||
chr2:74066268
|
C | T | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-7281C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066268 | ||||||
chr2:74066598
|
C | A | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2495-6951C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066598 | ||||||
chr2:74066598
|
C | CAA | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2495-6951_2495-695 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066598 | ||||||
chr2:74066787
|
T | A | 1 | a0001c0003t0010g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2495-6762T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066787 | ||||||
chr2:74066983
|
A | T | 88 | a0001c0001t0001g0057a0001c0002t0001g0005a0001c0002t0001g0079others(85): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2495-6566A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74066983 | ||||||
chr2:74067094
|
T | C | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2495-6455T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067094 | ||||||
chr2:74067155
|
C | T | 46 | a0001c0002t0001g0183a0001c0002t0003g0194a0001c0002t0003g0196others(43): Show | 47 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2495-6394C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067155 | ||||||
chr2:74067279
|
G | A | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-6270G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067279 | ||||||
chr2:74067290
|
A | C | 8 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0052g0182others(5): Show | 8 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-6259A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067290 | ||||||
chr2:74067322
|
T | G | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-6227T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067322 | ||||||
chr2:74067394
|
A | G | 1 | a0001c0002t0003g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2495-6155A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067394 | ||||||
chr2:74067527
|
A | G | 101 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2495-6022A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067527 | ||||||
chr2:74067557
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2495-5992C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067557 | ||||||
chr2:74067567
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2495-5982A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067567 | ||||||
chr2:74067721
|
G | A | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-5828G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74067721 | ||||||
chr2:74068006
|
C | T | 1 | a0001c0008t0002g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2495-5543C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068006 | ||||||
chr2:74068092
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2495-5457G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068092 | ||||||
chr2:74068094
|
C | A | 1 | a0001c0001t0041g0042 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2495-5455C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068094 | ||||||
chr2:74068168
|
G | A | 1 | a0001c0001t0004g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2495-5381G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068168 | ||||||
chr2:74068200
|
A | AT | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-5341dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74068200 | |||||
chr2:74068274
|
CAT | C | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-5272_2495-527 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74068274 | |||||
chr2:74068344
|
C | CTG | 102 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2495-5204_2495-520 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74068344 | |||||
chr2:74068422
|
T | A | 1 | a0001c0002t0002g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2495-5127T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068422 | ||||||
chr2:74068556
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-4993A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068556 | ||||||
chr2:74068589
|
A | G | 14 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-4960A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068589 | ||||||
chr2:74068635
|
T | A | 2 | a0001c0001t0002g0099a0007c0023t0001g0026 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2495-4914T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068635 | ||||||
chr2:74068744
|
C | G | 1 | a0001c0002t0026g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2495-4805C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068744 | ||||||
chr2:74068832
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2495-4717G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068832 | ||||||
chr2:74068860
|
C | T | 6 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-4689C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068860 | ||||||
chr2:74068902
|
A | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-4647A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74068902 | ||||||
chr2:74069122
|
C | G | 1 | a0008c0024t0001g0046 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2495-4427C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74069122 | ||||||
chr2:74069145
|
AT | A | 109 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2495-4393delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74069145 | |||||
chr2:74069284
|
G | A | 87 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2495-4265G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74069284 | ||||||
chr2:74069332
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2495-4217C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74069332 | ||||||
chr2:74069503
|
A | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-4046A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74069503 | ||||||
chr2:74069888
|
G | A | 1 | a0001c0001t0009g0104 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2495-3661G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74069888 | ||||||
chr2:74070003
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-3546A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070003 | ||||||
chr2:74070103
|
C | T | 10 | a0001c0002t0001g0005a0001c0002t0018g0137a0001c0002t0018g0139others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-3446C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070103 | ||||||
chr2:74070133
|
A | T | 4 | a0001c0002t0005g0072a0001c0002t0005g0074a0001c0002t0057g0073others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-3416A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070133 | ||||||
chr2:74070161
|
C | T | 100 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2495-3388C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070161 | ||||||
chr2:74070207
|
T | TG | 60 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0056others(57): Show | 60 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.2495-3339dupG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74070207 | |||||
chr2:74070538
|
C | T | 1 | a0001c0002t0024g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2495-3011C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070538 | ||||||
chr2:74070760
|
G | A | 1 | a0001c0001t0005g0155 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2495-2789G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74070760 | ||||||
chr2:74071036
|
A | G | 1 | a0001c0014t0044g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2495-2513A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071036 | ||||||
chr2:74071084
|
C | A | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2495-2465C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071084 | ||||||
chr2:74071657
|
A | G | 1 | a0001c0013t0054g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2495-1892A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071657 | ||||||
chr2:74071722
|
T | G | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-1827T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071722 | ||||||
chr2:74071829
|
G | A | 1 | a0001c0001t0005g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2495-1720G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071829 | ||||||
chr2:74071831
|
T | C | 110 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2495-1718T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071831 | ||||||
chr2:74071867
|
C | G | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-1682C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071867 | ||||||
chr2:74071905
|
G | A | 109 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2495-1644G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74071905 | ||||||
chr2:74072043
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-1506T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072043 | ||||||
chr2:74072253
|
C | T | 2 | a0001c0002t0008g0015a0001c0002t0008g0018 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2495-1296C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072253 | ||||||
chr2:74072295
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2495-1254C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072295 | ||||||
chr2:74072436
|
T | C | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2495-1113T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072436 | ||||||
chr2:74072440
|
A | T | 5 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0117others(2): Show | 5 | HG00438.hp2 HG00673.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495-1109A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072440 | ||||||
chr2:74072444
|
G | A | 7 | a0001c0002t0013g0236a0001c0002t0015g0238a0001c0002t0015g0243others(4): Show | 7 | HG00735.hp2 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2495-1105G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072444 | ||||||
chr2:74072511
|
T | TA | 7 | a0001c0001t0001g0066a0001c0001t0001g0180a0001c0001t0006g0231others(4): Show | 7 | HG00423.hp1 HG00423.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-1021dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 74072511 | |||||
chr2:74072664
|
A | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-885A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072664 | ||||||
chr2:74072969
|
C | T | 10 | a0001c0002t0008g0015a0001c0002t0008g0017a0001c0002t0008g0018others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-580C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74072969 | ||||||
chr2:74073132
|
C | A | 1 | a0001c0002t0003g0207 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2495-417C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74073132 | ||||||
chr2:74073214
|
G | A | 1 | a0001c0001t0037g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2495-335G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74073214 | ||||||
chr2:74073496
|
T | C | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG01099.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2495-53T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 4/11 | chr2 | 74073496 | ||||||
chr2:74073680
|
G | A | 1 | a0001c0002t0003g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2585+41G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74073680 | ||||||
chr2:74073704
|
G | A | 1 | a0001c0007t0033g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2585+65G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74073704 | ||||||
chr2:74073728
|
A | C | 3 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221 | 3 | HG02055.hp2 HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2585+89A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74073728 | ||||||
chr2:74073848
|
C | T | 1 | a0001c0002t0012g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2585+209C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74073848 | ||||||
chr2:74074138
|
C | T | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2585+499C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074138 | ||||||
chr2:74074162
|
G | A | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2585+523G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074162 | ||||||
chr2:74074230
|
A | G | 1 | a0001c0001t0004g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2585+591A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074230 | ||||||
chr2:74074688
|
A | T | 2 | a0001c0002t0004g0129a0001c0002t0004g0130 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2585+1049A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074688 | ||||||
chr2:74074713
|
G | T | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2585+1074G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074713 | ||||||
chr2:74074720
|
G | A | 1 | a0001c0001t0041g0042 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2585+1081G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074720 | ||||||
chr2:74074754
|
A | AAC | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2585+1118_2585+111 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74074754 | |||||
chr2:74074840
|
G | A | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2585+1201G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074840 | ||||||
chr2:74074882
|
G | GT | 108 | a0001c0001t0004g0076a0001c0002t0001g0005a0001c0002t0001g0009others(105): Show | 109 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.2585+1252dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74074882 | |||||
chr2:74074896
|
C | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2585+1257C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74074896 | ||||||
chr2:74075113
|
G | A | 2 | a0001c0002t0014g0001a0001c0002t0014g0223 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2585+1474G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075113 | ||||||
chr2:74075131
|
A | G | 1 | a0001c0002t0005g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2585+1492A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075131 | ||||||
chr2:74075161
|
C | T | 6 | a0001c0002t0001g0135a0001c0002t0004g0129a0001c0002t0004g0130others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2585+1522C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075161 | ||||||
chr2:74075213
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2585+1574A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075213 | ||||||
chr2:74075320
|
C | CT | 38 | a0001c0001t0001g0034a0001c0001t0001g0151a0001c0001t0001g0154others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2585+1708dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74075320 | |||||
chr2:74075320
|
C | CTT | 7 | a0001c0001t0004g0088a0001c0002t0001g0183a0001c0002t0005g0072others(4): Show | 7 | HG01884.hp1 HG02056.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2585+1707_2585+170 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74075320 | |||||
chr2:74075320
|
CT | C | 9 | a0001c0001t0001g0150a0001c0001t0001g0162a0001c0002t0004g0130others(6): Show | 9 | HG00323.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2585+1708delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74075320 | |||||
chr2:74075320
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2585+1697_2585+170 others(16): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74075320 | |||||
chr2:74075320
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0019t0004g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2585+1696_2585+170 others(17): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74075320 | |||||
chr2:74075371
|
C | T | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2585+1732C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075371 | ||||||
chr2:74075404
|
C | T | 2 | a0001c0002t0003g0197a0001c0002t0012g0204 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2585+1765C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075404 | ||||||
chr2:74075435
|
T | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2585+1796T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075435 | ||||||
chr2:74075577
|
C | T | 1 | a0001c0001t0006g0201 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2585+1938C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075577 | ||||||
chr2:74075714
|
A | G | 1 | a0001c0003t0013g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2585+2075A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075714 | ||||||
chr2:74075817
|
G | A | 1 | a0001c0001t0004g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2585+2178G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74075817 | ||||||
chr2:74076056
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2585+2417G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076056 | ||||||
chr2:74076076
|
A | T | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2585+2437A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076076 | ||||||
chr2:74076125
|
C | G | 2 | a0001c0001t0004g0088a0001c0001t0051g0025 | 2 | HG02056.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2585+2486C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076125 | ||||||
chr2:74076159
|
C | CT | 24 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(21): Show | 24 | HG00558.hp2 HG01070.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.2585+2531dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076159 | |||||
chr2:74076339
|
G | A | 1 | a0001c0002t0003g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2585+2700G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076339 | ||||||
chr2:74076375
|
C | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2585+2736C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076375 | ||||||
chr2:74076441
|
G | GT | 18 | a0001c0001t0001g0027a0001c0001t0002g0052a0001c0001t0002g0118others(15): Show | 18 | HG00423.hp2 HG00438.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2585+2831dupT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
G | GTTTTTTT others(4): Show |
1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2585+2821_2585+283 others(15): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GT | G | 55 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0033others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.2585+2831delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GTT | G | 29 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0005g0032others(26): Show | 30 | HG00558.hp2 HG00741.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2585+2830_2585+283 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GTTT | G | 20 | a0001c0001t0005g0125a0001c0002t0001g0079a0001c0002t0001g0080others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.2585+2829_2585+283 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GTTTT | G | 20 | a0001c0001t0022g0063a0001c0002t0001g0183a0001c0002t0002g0128others(17): Show | 20 | HG00323.hp1 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.2585+2828_2585+283 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GTTTTT | G | 29 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(26): Show | 29 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.2585+2827_2585+283 others(9): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076441
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2585+2822_2585+283 others(14): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74076441 | |||||
chr2:74076452
|
T | G | 1 | a0001c0002t0060g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2585+2813T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076452 | ||||||
chr2:74076461
|
T | G | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2585+2822T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076461 | ||||||
chr2:74076466
|
T | G | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2585+2827T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076466 | ||||||
chr2:74076592
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2585+2953T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076592 | ||||||
chr2:74076796
|
T | C | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2585+3157T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076796 | ||||||
chr2:74076843
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0002g0146 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2585+3204G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076843 | ||||||
chr2:74076885
|
C | G | 13 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2585+3246C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076885 | ||||||
chr2:74076975
|
C | G | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2585+3336C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74076975 | ||||||
chr2:74077015
|
A | G | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2585+3376A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077015 | ||||||
chr2:74077019
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2585+3380C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077019 | ||||||
chr2:74077251
|
C | G | 87 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2586-3247C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077251 | ||||||
chr2:74077380
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2586-3118C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077380 | ||||||
chr2:74077440
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2586-3058A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077440 | ||||||
chr2:74077616
|
CTGTTTT | C | 8 | a0001c0002t0003g0197a0001c0002t0011g0206a0001c0002t0012g0188others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2586-2862_2586-285 others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 74077616 | |||||
chr2:74077762
|
A | G | 8 | a0001c0002t0003g0197a0001c0002t0011g0206a0001c0002t0012g0188others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2586-2736A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077762 | ||||||
chr2:74077795
|
G | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2586-2703G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077795 | ||||||
chr2:74077960
|
T | A | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2586-2538T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74077960 | ||||||
chr2:74078076
|
G | C | 109 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2586-2422G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078076 | ||||||
chr2:74078160
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2586-2338T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078160 | ||||||
chr2:74078198
|
G | A | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2586-2300G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078198 | ||||||
chr2:74078347
|
A | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2586-2151A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078347 | ||||||
chr2:74078438
|
C | A | 1 | a0001c0004t0003g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2586-2060C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078438 | ||||||
chr2:74078438
|
C | G | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2586-2060C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078438 | ||||||
chr2:74078471
|
T | A | 1 | a0001c0002t0005g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2586-2027T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078471 | ||||||
chr2:74078797
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2586-1701A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078797 | ||||||
chr2:74078883
|
A | G | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2586-1615A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078883 | ||||||
chr2:74078929
|
G | A | 108 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2586-1569G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74078929 | ||||||
chr2:74079078
|
G | C | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2586-1420G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079078 | ||||||
chr2:74079175
|
T | C | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2586-1323T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079175 | ||||||
chr2:74079271
|
G | A | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2586-1227G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079271 | ||||||
chr2:74079426
|
A | G | 1 | a0001c0002t0028g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2586-1072A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079426 | ||||||
chr2:74079526
|
A | T | 4 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2586-972A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079526 | ||||||
chr2:74079887
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18747.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.2586-611A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079887 | ||||||
chr2:74079990
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2586-508G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74079990 | ||||||
chr2:74080070
|
A | G | 87 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2586-428A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74080070 | ||||||
chr2:74080102
|
C | T | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2586-396C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74080102 | ||||||
chr2:74080307
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2586-191C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 5/11 | chr2 | 74080307 | ||||||
chr2:74080629
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679+38T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080629 | ||||||
chr2:74080642
|
T | G | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2679+51T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080642 | ||||||
chr2:74080670
|
C | G | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2679+79C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080670 | ||||||
chr2:74080694
|
G | A | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679+103G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080694 | ||||||
chr2:74080694
|
G | T | 2 | a0001c0009t0005g0168a0001c0009t0034g0167 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2679+103G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080694 | ||||||
chr2:74080699
|
C | CG | 11 | a0001c0002t0003g0194a0001c0002t0003g0207a0001c0002t0003g0214others(8): Show | 11 | HG01175.hp2 HG01934.hp1 NA18522.hp2 others(8): Show |
intron_variant | MODIFIER | c.2679+114dupG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74080699 | |||||
chr2:74080699
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679+108C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080699 | ||||||
chr2:74080705
|
G | T | 40 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(37): Show | 40 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2679+114G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080705 | ||||||
chr2:74080705
|
GT | G | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2679+115delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080705 | ||||||
chr2:74080706
|
T | G | 108 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2679+115T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080706 | ||||||
chr2:74080708
|
G | C | 13 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(10): Show | 13 | HG00735.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2679+117G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080708 | ||||||
chr2:74080776
|
C | A | 1 | a0001c0001t0006g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2679+185C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080776 | ||||||
chr2:74080777
|
A | G | 1 | a0001c0001t0006g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2679+186A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080777 | ||||||
chr2:74080879
|
A | G | 1 | a0001c0002t0002g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2679+288A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080879 | ||||||
chr2:74080942
|
G | C | 7 | a0001c0002t0003g0197a0001c0002t0012g0188a0001c0002t0012g0189others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2679+351G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74080942 | ||||||
chr2:74081054
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2679+463G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74081054 | ||||||
chr2:74081102
|
G | A | 11 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0064others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.2679+511G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74081102 | ||||||
chr2:74081110
|
C | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679+519C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74081110 | ||||||
chr2:74081169
|
C | T | 2 | a0001c0001t0005g0125a0001c0001t0022g0063 | 2 | HG00621.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2679+578C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74081169 | ||||||
chr2:74081867
|
T | C | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2679+1276T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74081867 | ||||||
chr2:74082257
|
C | T | 1 | a0001c0008t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2679+1666C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082257 | ||||||
chr2:74082258
|
G | A | 1 | a0001c0002t0045g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2679+1667G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082258 | ||||||
chr2:74082274
|
G | A | 88 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(85): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2679+1683G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082274 | ||||||
chr2:74082356
|
A | G | 1 | a0001c0021t0005g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2679+1765A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082356 | ||||||
chr2:74082414
|
G | T | 2 | a0001c0002t0005g0140a0001c0002t0019g0186 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2679+1823G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082414 | ||||||
chr2:74082442
|
A | G | 4 | a0001c0002t0005g0072a0001c0002t0005g0074a0001c0002t0057g0073others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2679+1851A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082442 | ||||||
chr2:74082539
|
T | C | 23 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0085others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.2679+1948T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082539 | ||||||
chr2:74082566
|
T | TA | 47 | a0001c0002t0001g0183a0001c0002t0003g0194a0001c0002t0003g0196others(44): Show | 48 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.2679+1976dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74082566 | |||||
chr2:74082631
|
G | A | 43 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(40): Show | 44 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2679+2040G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082631 | ||||||
chr2:74082783
|
G | A | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2679+2192G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082783 | ||||||
chr2:74082860
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2679+2269C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74082860 | ||||||
chr2:74083009
|
C | T | 1 | a0001c0002t0016g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2679+2418C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083009 | ||||||
chr2:74083152
|
AG | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0005g0032 | 3 | HG01081.hp1 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2679+2562delG | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083152 | ||||||
chr2:74083524
|
C | G | 1 | a0004c0022t0049g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2679+2933C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083524 | ||||||
chr2:74083572
|
T | C | 1 | a0001c0004t0025g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2679+2981T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083572 | ||||||
chr2:74083657
|
A | G | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679+3066A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083657 | ||||||
chr2:74083660
|
C | G | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2679+3069C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083660 | ||||||
chr2:74083918
|
C | T | 2 | a0001c0002t0011g0222a0005c0011t0011g0235 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2679+3327C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083918 | ||||||
chr2:74083938
|
C | T | 88 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(85): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2679+3347C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74083938 | ||||||
chr2:74084082
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2679+3491C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084082 | ||||||
chr2:74084203
|
A | G | 1 | a0001c0001t0004g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2679+3612A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084203 | ||||||
chr2:74084216
|
A | T | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2680-3614A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084216 | ||||||
chr2:74084425
|
A | G | 1 | a0001c0001t0005g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2680-3405A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084425 | ||||||
chr2:74084435
|
T | C | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2680-3395T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084435 | ||||||
chr2:74084473
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0158 | 2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2680-3357G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084473 | ||||||
chr2:74084598
|
G | A | 1 | a0001c0002t0024g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2680-3232G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084598 | ||||||
chr2:74084699
|
C | T | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2680-3131C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084699 | ||||||
chr2:74084728
|
C | T | 1 | a0003c0025t0030g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2680-3102C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084728 | ||||||
chr2:74084915
|
A | G | 1 | a0001c0001t0002g0101 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2680-2915A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74084915 | ||||||
chr2:74085086
|
A | G | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2680-2744A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085086 | ||||||
chr2:74085138
|
A | C | 12 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2680-2692A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085138 | ||||||
chr2:74085150
|
C | CA | 45 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0158others(42): Show | 46 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2680-2666dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74085150 | |||||
chr2:74085150
|
CA | C | 6 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2680-2666delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74085150 | |||||
chr2:74085290
|
C | T | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2680-2540C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085290 | ||||||
chr2:74085412
|
C | T | 29 | a0001c0002t0003g0194a0001c0002t0003g0196a0001c0002t0003g0198others(26): Show | 29 | HG00558.hp2 HG01070.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2680-2418C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085412 | ||||||
chr2:74085567
|
G | A | 2 | a0001c0002t0005g0065a0001c0002t0036g0089 | 2 | HG00673.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2680-2263G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085567 | ||||||
chr2:74085576
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0026g0205a0001c0002t0028g0239 | 3 | HG02895.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2680-2254C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085576 | ||||||
chr2:74085616
|
T | G | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2680-2214T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085616 | ||||||
chr2:74085626
|
T | C | 1 | a0001c0002t0002g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2680-2204T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085626 | ||||||
chr2:74085631
|
A | AGTTCACA others(5): Show |
117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2680-2194_2680-219 others(16): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74085631 | |||||
chr2:74085674
|
AGGAGGTG others(11): Show |
A | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2680-2154_2680-213 others(22): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74085674 | |||||
chr2:74085689
|
G | C | 3 | a0001c0001t0005g0061a0001c0001t0005g0071a0001c0001t0005g0249 | 3 | HG01175.hp1 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2680-2141G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085689 | ||||||
chr2:74085953
|
T | C | 191 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0029others(188): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2680-1877T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74085953 | ||||||
chr2:74086112
|
C | A | 1 | a0001c0013t0054g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2680-1718C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74086112 | ||||||
chr2:74086143
|
G | A | 2 | a0001c0002t0001g0009a0001c0002t0001g0010 | 2 | HG01099.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2680-1687G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74086143 | ||||||
chr2:74086379
|
TA | T | 9 | a0001c0001t0002g0052a0001c0001t0004g0069a0001c0001t0021g0191others(6): Show | 9 | HG01517.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2680-1438delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086379 | |||||
chr2:74086566
|
T | G | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2680-1264T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74086566 | ||||||
chr2:74086791
|
T | TA | 10 | a0001c0001t0001g0176a0001c0001t0002g0117a0001c0001t0004g0055others(7): Show | 10 | HG01070.hp2 HG02074.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2680-1017dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086791 | |||||
chr2:74086791
|
T | TAA | 61 | a0001c0002t0001g0005a0001c0002t0001g0135a0001c0002t0001g0183others(58): Show | 62 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.2680-1018_2680-101 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086791 | |||||
chr2:74086791
|
T | TAAA | 21 | a0001c0002t0001g0079a0001c0002t0001g0085a0001c0002t0002g0093others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2680-1019_2680-101 others(7): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086791 | |||||
chr2:74086791
|
T | TAAAA | 5 | a0001c0002t0001g0080a0001c0002t0002g0087a0001c0002t0005g0072others(2): Show | 5 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.2680-1020_2680-101 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086791 | |||||
chr2:74086791
|
TA | T | 25 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0151others(22): Show | 25 | HG00280.hp2 HG00438.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.2680-1017delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 74086791 | |||||
chr2:74086954
|
A | G | 15 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2680-876A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74086954 | ||||||
chr2:74087262
|
T | C | 1 | a0001c0003t0013g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2680-568T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087262 | ||||||
chr2:74087614
|
T | C | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2680-216T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087614 | ||||||
chr2:74087634
|
G | T | 29 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0085others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2680-196G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087634 | ||||||
chr2:74087740
|
C | T | 1 | a0001c0010t0004g0166 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2680-90C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087740 | ||||||
chr2:74087788
|
C | T | 1 | a0001c0002t0006g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2680-42C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087788 | ||||||
chr2:74087819
|
C | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2680-11C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 6/11 | chr2 | 74087819 | ||||||
chr2:74088231
|
C | A | 1 | a0001c0002t0057g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2888+193C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088231 | ||||||
chr2:74088258
|
C | A | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2888+220C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088258 | ||||||
chr2:74088388
|
A | G | 1 | a0001c0001t0005g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2888+350A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088388 | ||||||
chr2:74088791
|
T | C | 56 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(53): Show | 57 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2888+753T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088791 | ||||||
chr2:74088829
|
G | A | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2888+791G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088829 | ||||||
chr2:74088950
|
A | G | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0029others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2888+912A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088950 | ||||||
chr2:74088982
|
G | A | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2889-915G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74088982 | ||||||
chr2:74089080
|
C | CA | 8 | a0001c0001t0001g0053a0001c0001t0001g0103a0001c0001t0001g0172others(5): Show | 8 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.2889-793dupA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 74089080 | |||||
chr2:74089080
|
CA | C | 63 | a0001c0001t0001g0153a0001c0001t0004g0051a0001c0001t0004g0055others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.2889-793delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 74089080 | |||||
chr2:74089104
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2889-793A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089104 | ||||||
chr2:74089190
|
G | A | 1 | a0001c0003t0050g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2889-707G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089190 | ||||||
chr2:74089190
|
G | C | 2 | a0001c0002t0014g0001a0001c0002t0014g0223 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889-707G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089190 | ||||||
chr2:74089287
|
A | C | 41 | a0001c0002t0001g0005a0001c0002t0001g0079a0001c0002t0001g0080others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2889-610A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089287 | ||||||
chr2:74089529
|
A | G | 14 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2889-368A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089529 | ||||||
chr2:74089600
|
A | G | 2 | a0001c0002t0014g0001a0001c0002t0014g0223 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889-297A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 7/11 | chr2 | 74089600 | ||||||
chr2:74090170
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3039+123G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090170 | ||||||
chr2:74090214
|
T | C | 1 | a0001c0004t0002g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3039+167T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090214 | ||||||
chr2:74090324
|
A | C | 1 | a0001c0006t0001g0251 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3039+277A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090324 | ||||||
chr2:74090373
|
C | A | 54 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(51): Show | 55 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.3039+326C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090373 | ||||||
chr2:74090374
|
C | G | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3039+327C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090374 | ||||||
chr2:74090422
|
G | A | 1 | a0001c0007t0033g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3039+375G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090422 | ||||||
chr2:74090452
|
C | T | 1 | a0001c0001t0006g0247 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3039+405C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090452 | ||||||
chr2:74090553
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3039+506G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090553 | ||||||
chr2:74090554
|
C | A | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3039+507C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090554 | ||||||
chr2:74090605
|
G | A | 1 | a0006c0012t0027g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3039+558G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090605 | ||||||
chr2:74090620
|
T | C | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3039+573T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090620 | ||||||
chr2:74090678
|
G | T | 7 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3039+631G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090678 | ||||||
chr2:74090781
|
G | A | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3039+734G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74090781 | ||||||
chr2:74091156
|
T | C | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3039+1109T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091156 | ||||||
chr2:74091323
|
A | G | 5 | a0001c0001t0001g0043a0001c0006t0001g0251a0001c0006t0005g0248others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.3039+1276A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091323 | ||||||
chr2:74091324
|
C | G | 61 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(58): Show | 62 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.3039+1277C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091324 | ||||||
chr2:74091346
|
G | A | 2 | a0001c0002t0014g0001a0001c0002t0014g0223 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3039+1299G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091346 | ||||||
chr2:74091477
|
G | T | 14 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0014others(11): Show | 14 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.3040-1425G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091477 | ||||||
chr2:74091582
|
G | A | 1 | a0001c0006t0005g0248 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3040-1320G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091582 | ||||||
chr2:74091642
|
C | T | 4 | a0001c0002t0015g0238a0001c0002t0015g0243a0001c0003t0029g0242others(1): Show | 4 | HG00735.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3040-1260C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091642 | ||||||
chr2:74091653
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3040-1249G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091653 | ||||||
chr2:74091680
|
C | T | 10 | a0001c0002t0001g0005a0001c0002t0018g0137a0001c0002t0018g0139others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3040-1222C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091680 | ||||||
chr2:74091910
|
GT | G | 117 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3040-991delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091910 | ||||||
chr2:74091937
|
C | G | 2 | a0001c0001t0002g0099a0007c0023t0001g0026 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.3040-965C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091937 | ||||||
chr2:74091973
|
G | A | 1 | a0001c0002t0014g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3040-929G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091973 | ||||||
chr2:74091986
|
A | G | 48 | a0001c0002t0001g0183a0001c0002t0003g0194a0001c0002t0003g0196others(45): Show | 49 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.3040-916A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74091986 | ||||||
chr2:74092042
|
G | A | 1 | a0001c0016t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3040-860G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74092042 | ||||||
chr2:74092343
|
T | A | 60 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0001t0063g0221others(57): Show | 61 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.3040-559T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74092343 | ||||||
chr2:74092678
|
C | T | 44 | a0001c0002t0001g0183a0001c0002t0003g0194a0001c0002t0003g0196others(41): Show | 44 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.3040-224C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74092678 | ||||||
chr2:74092831
|
A | C | 1 | a0001c0002t0011g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3040-71A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 8/11 | chr2 | 74092831 | ||||||
chr2:74093135
|
C | G | 103 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(100): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3129+144C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 9/11 | chr2 | 74093135 | ||||||
chr2:74093705
|
A | G | 11 | a0001c0001t0020g0095a0001c0002t0001g0005a0001c0002t0001g0014others(8): Show | 11 | HG00735.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3267+39A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74093705 | ||||||
chr2:74093819
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3267+153C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74093819 | ||||||
chr2:74093821
|
C | T | 1 | a0001c0002t0042g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3267+155C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74093821 | ||||||
chr2:74093948
|
G | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.3267+282G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74093948 | ||||||
chr2:74094178
|
T | C | 3 | a0001c0002t0011g0206a0001c0002t0014g0001a0001c0002t0014g0223 | 4 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267+512T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094178 | ||||||
chr2:74094382
|
T | C | 1 | a0001c0002t0062g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3267+716T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094382 | ||||||
chr2:74094529
|
C | T | 1 | a0001c0002t0005g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3267+863C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094529 | ||||||
chr2:74094647
|
C | T | 3 | a0001c0002t0001g0183a0001c0002t0020g0184a0001c0002t0038g0185 | 3 | HG02257.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3267+981C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094647 | ||||||
chr2:74094663
|
G | T | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3267+997G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094663 | ||||||
chr2:74094746
|
G | T | 8 | a0001c0002t0001g0005a0001c0002t0048g0002a0001c0003t0010g0003others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3267+1080G>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094746 | ||||||
chr2:74094831
|
G | A | 1 | a0001c0002t0046g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3267+1165G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74094831 | ||||||
chr2:74095022
|
T | C | 2 | a0001c0001t0004g0123a0001c0010t0004g0166 | 2 | NA18977.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3267+1356T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095022 | ||||||
chr2:74095117
|
A | G | 89 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.3267+1451A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095117 | ||||||
chr2:74095342
|
C | T | 161 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0098others(158): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.3267+1676C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095342 | ||||||
chr2:74095377
|
A | C | 1 | a0001c0001t0002g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3267+1711A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095377 | ||||||
chr2:74095710
|
T | C | 1 | a0001c0002t0023g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3267+2044T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095710 | ||||||
chr2:74095840
|
C | G | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3267+2174C>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74095840 | ||||||
chr2:74096157
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3267+2491T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096157 | ||||||
chr2:74096271
|
G | C | 3 | a0001c0002t0014g0001a0001c0002t0014g0223a0001c0002t0042g0013 | 4 | HG02280.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267+2605G>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096271 | ||||||
chr2:74096373
|
G | A | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(65): Show | 68 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.3267+2707G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096373 | ||||||
chr2:74096384
|
A | T | 1 | a0001c0019t0004g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3267+2718A>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096384 | ||||||
chr2:74096540
|
G | A | 3 | a0001c0002t0018g0137a0001c0002t0018g0139a0001c0015t0043g0136 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3268-2736G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096540 | ||||||
chr2:74096768
|
CA | C | 80 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(77): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.3268-2496delA | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74096768 | |||||
chr2:74096910
|
G | A | 3 | a0001c0002t0014g0001a0001c0002t0014g0223a0001c0002t0042g0013 | 4 | HG02280.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3268-2366G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096910 | ||||||
chr2:74096977
|
C | T | 1 | a0001c0015t0043g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3268-2299C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74096977 | ||||||
chr2:74097050
|
C | A | 5 | a0001c0002t0011g0206a0001c0002t0014g0001a0001c0002t0014g0223others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3268-2226C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097050 | ||||||
chr2:74097088
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3268-2188T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097088 | ||||||
chr2:74097122
|
AAAAG | A | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3268-2150_3268-214 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097122 | |||||
chr2:74097195
|
G | GCA | 27 | a0001c0001t0001g0044a0001c0001t0002g0117a0001c0001t0005g0061others(24): Show | 27 | HG00735.hp2 HG01192.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.3268-2046_3268-204 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACA | 26 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0059others(23): Show | 26 | HG00558.hp2 HG00741.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.3268-2048_3268-204 others(8): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACACA | 7 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG00621.hp2 HG02280.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.3268-2050_3268-204 others(10): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACACAC others(1): Show |
32 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0029others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.3268-2052_3268-204 others(12): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACACAC others(3): Show |
18 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0075others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.3268-2054_3268-204 others(14): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACACAC others(5): Show |
5 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0143others(2): Show | 5 | HG00280.hp2 HG00738.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.3268-2056_3268-204 others(16): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
G | GCACACAC others(7): Show |
2 | a0001c0001t0040g0049a0001c0002t0001g0080 | 2 | HG00140.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.3268-2058_3268-204 others(18): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
GCA | G | 13 | a0001c0001t0001g0068a0001c0001t0004g0091a0001c0001t0004g0102others(10): Show | 13 | HG00673.hp2 HG01993.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.3268-2046_3268-204 others(6): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
GCACACAC others(1): Show |
G | 6 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0158others(3): Show | 6 | HG02083.hp1 HG02922.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.3268-2052_3268-204 others(12): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0153 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3268-2054_3268-204 others(14): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097195
|
GCACACAC others(13): Show |
G | 2 | a0001c0002t0011g0206a0001c0002t0020g0184 | 2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3268-2064_3268-204 others(24): Show |
TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74097195 | |||||
chr2:74097232
|
T | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0021g0191others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.3268-2044T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097232 | ||||||
chr2:74097377
|
C | T | 66 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.3268-1899C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097377 | ||||||
chr2:74097550
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA18747.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3268-1726A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097550 | ||||||
chr2:74097555
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3268-1721C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097555 | ||||||
chr2:74097627
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3268-1649C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097627 | ||||||
chr2:74097870
|
T | C | 63 | a0001c0001t0001g0100a0001c0001t0001g0172a0001c0001t0001g0173others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.3268-1406T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74097870 | ||||||
chr2:74098038
|
C | T | 21 | a0001c0001t0021g0191a0001c0001t0021g0192a0001c0002t0012g0188others(18): Show | 22 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3268-1238C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098038 | ||||||
chr2:74098064
|
A | C | 1 | a0002c0005t0002g0127 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3268-1212A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098064 | ||||||
chr2:74098095
|
A | G | 1 | a0001c0002t0003g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3268-1181A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098095 | ||||||
chr2:74098489
|
T | C | 1 | a0001c0002t0039g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3268-787T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098489 | ||||||
chr2:74098527
|
T | G | 29 | a0001c0001t0001g0098a0001c0001t0001g0158a0001c0001t0002g0099others(26): Show | 29 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.3268-749T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098527 | ||||||
chr2:74098578
|
T | G | 35 | a0001c0001t0001g0100a0001c0001t0005g0032a0001c0001t0063g0221others(32): Show | 35 | HG01070.hp1 HG01099.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.3268-698T>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098578 | ||||||
chr2:74098595
|
TC | T | 9 | a0001c0002t0004g0129a0001c0002t0004g0130a0001c0002t0035g0092others(6): Show | 9 | HG01192.hp2 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.3268-680delC | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098595 | ||||||
chr2:74098596
|
C | T | 75 | a0001c0001t0001g0068a0001c0001t0001g0111a0001c0001t0001g0176others(72): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.3268-680C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098596 | ||||||
chr2:74098596
|
CT | C | 93 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0158others(90): Show | 94 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3268-665delT | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 74098596 | |||||
chr2:74098649
|
T | C | 1 | a0001c0001t0004g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3268-627T>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098649 | ||||||
chr2:74098683
|
C | A | 1 | a0001c0001t0019g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3268-593C>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098683 | ||||||
chr2:74098866
|
A | G | 1 | a0001c0002t0035g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3268-410A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74098866 | ||||||
chr2:74099051
|
A | C | 1 | a0002c0005t0002g0149 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3268-225A>C | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74099051 | ||||||
chr2:74099110
|
G | A | 7 | a0001c0003t0010g0003a0001c0003t0010g0016a0001c0003t0010g0107others(4): Show | 7 | HG00735.hp2 HG01192.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3268-166G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74099110 | ||||||
chr2:74099232
|
G | A | 1 | a0001c0003t0010g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3268-44G>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 10/11 | chr2 | 74099232 | ||||||
chr2:74099669
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3604+57C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74099669 | ||||||
chr2:74099775
|
C | T | 177 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0111others(174): Show | 178 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.3604+163C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74099775 | ||||||
chr2:74099898
|
A | G | 3 | a0001c0002t0019g0186a0001c0002t0028g0239a0001c0002t0048g0002 | 3 | HG02922.hp1 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3604+286A>G | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74099898 | ||||||
chr2:74100013
|
C | T | 30 | a0001c0001t0001g0100a0001c0001t0063g0221a0001c0002t0001g0009others(27): Show | 30 | HG01070.hp1 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.3605-380C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74100013 | ||||||
chr2:74100102
|
T | A | 7 | a0001c0004t0002g0006a0001c0004t0002g0007a0001c0004t0002g0008others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3605-291T>A | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74100102 | ||||||
chr2:74100326
|
C | T | 32 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0158others(29): Show | 32 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3605-67C>T | TET3 | ENSG00000187605.16 | transcript | ENST00000409262.8 | protein_coding | 11/11 | chr2 | 74100326 |