geneid | 25828 |
---|---|
ensemblid | ENSG00000100348.10 |
hgncid | 17772 |
symbol | TXN2 |
name | thioredoxin 2 |
refseq_nuc | NM_012473.4 |
refseq_prot | NP_036605.2 |
ensembl_nuc | ENST00000216185.7 |
ensembl_prot | ENSP00000216185.2 |
mane_status | MANE Select |
chr | chr22 |
start | 36467046 |
end | 36481640 |
strand | - |
ver | v1.2 |
region | chr22:36467046-36481640 |
region5000 | chr22:36462046-36486640 |
regionname0 | TXN2_chr22_36467046_36481640 |
regionname5000 | TXN2_chr22_36462046_36486640 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 166 | 338 | 93 | 62 | 137 | 10 | 34 | 115 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0002 | 0/0 | 166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0003 | 0/0 | 166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 501 | 334 | 91 | 60 | 137 | 10 | 34 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
c0002 | 0/0 | 501 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
c0003 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
c0004 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
c0005 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
c0006 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 836 | 266 | 74 | 52 | 99 | 9 | 30 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0002 | 0/0 | 836 | 31 | 0 | 6 | 25 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0003 | 0/0 | 836 | 17 | 14 | 2 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0004 | 0/0 | 836 | 13 | 2 | 0 | 10 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0005 | 0/0 | 836 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0006 | 0/0 | 836 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0007 | 0/0 | 836 | 2 | 0 | 0 | 0 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0008 | 0/0 | 836 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0009 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0010 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0011 | 0/0 | 836 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0012 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
t0013 | 0/0 | 836 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 53 | 2 | 7 | 33 | 0 | 10 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0002 | 0/0 | 32 | 1 | 16 | 7 | 4 | 4 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0003 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0005 | 0/0 | 11 | 4 | 3 | 0 | 2 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0010 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0015 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 501 | 334 | 91 | 60 | 137 | 10 | 34 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0002 | 0/0 | 501 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0003 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0005 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0002c0004 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0003c0006 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1336 | 260 | 71 | 50 | 98 | 9 | 30 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0002 | 0/0 | 1336 | 31 | 0 | 6 | 25 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0003 | 0/0 | 1336 | 17 | 14 | 2 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0004 | 0/0 | 1336 | 13 | 2 | 0 | 10 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0005 | 0/0 | 1336 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0006 | 0/0 | 1336 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0007 | 0/0 | 1336 | 2 | 0 | 0 | 0 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0008 | 0/0 | 1336 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0009 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0010 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0011 | 0/0 | 1336 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0012 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0001t0013 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0002t0001 | 0/0 | 1336 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0003t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0001c0005t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0002c0004t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
a0003c0006t0001 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | copy fasta | chr22 | 36462046 | 36486640 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 53 | 2 | 7 | 33 | 0 | 10 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0002 | 0/0 | 32 | 1 | 16 | 7 | 4 | 4 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0003 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0005 | 0/0 | 11 | 4 | 3 | 0 | 2 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0015 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
a0003c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0073 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03491 | hp2 | a0001 | c0001 | t0013 | g0149 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0126 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0122 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18522 | hp1 | a0002 | c0004 | t0001 | g0058 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18954 | hp2 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18962 | hp1 | a0001 | c0001 | t0012 | g0102 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18998 | hp2 | a0003 | c0006 | t0001 | g0148 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19010 | hp1 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0027 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02486 | hp1 | a0001 | c0005 | t0001 | g0147 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0109 | REF | REF | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:36476771
|
C | T | 1 | a0002 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.349G>A | p.Asp117Asn | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/4 | 426/1336 | 349/501 | 117/166 | chr22 | 36476771 | ||
chr22:36480682
|
T | C | 1 | a0003 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.156A>G | p.Ile52Met | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 233/1336 | 156/501 | 52/166 | chr22 | 36480682 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:36476826
|
C | T | 1 | a0001c0002 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.294G>A | p.Pro98Pro | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/4 | 371/1336 | 294/501 | 98/166 | chr22 | 36476826 | ||
chr22:36480580
|
G | A | 1 | a0001c0005 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.258C>T | p.His86His | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 335/1336 | 258/501 | 86/166 | chr22 | 36480580 | ||
chr22:36480805
|
C | T | 1 | a0001c0003 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.33G>A | p.Leu11Leu | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 110/1336 | 33/501 | 11/166 | chr22 | 36480805 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:36467049
|
G | A | 1 | a0001c0001t0007 | 2 | HG03688.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*755C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 755 | chr22 | 36467049 | |||||
chr22:36467099
|
G | T | 1 | a0001c0001t0008 | 2 | HG02818.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*705C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 705 | chr22 | 36467099 | |||||
chr22:36467113
|
C | T | 4 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(1): Show | 34 | HG01167.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 691 | chr22 | 36467113 | |||||
chr22:36467114
|
G | A | 1 | a0001c0001t0010 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 690 | chr22 | 36467114 | |||||
chr22:36467267
|
A | T | 1 | a0001c0001t0009 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 537 | chr22 | 36467267 | |||||
chr22:36467328
|
C | A | 1 | a0001c0001t0002 | 31 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*476G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 476 | chr22 | 36467328 | |||||
chr22:36467341
|
G | C | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 463 | chr22 | 36467341 | |||||
chr22:36467439
|
G | A | 1 | a0001c0001t0012 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 365 | chr22 | 36467439 | |||||
chr22:36467444
|
G | A | 3 | a0001c0001t0003a0001c0001t0004a0001c0001t0007 | 32 | HG01167.hp2 HG01168.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*360C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 360 | chr22 | 36467444 | |||||
chr22:36467552
|
T | C | 1 | a0001c0001t0013 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 252 | chr22 | 36467552 | |||||
chr22:36467658
|
C | T | 2 | a0001c0001t0004a0001c0001t0007 | 15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 146 | chr22 | 36467658 | |||||
chr22:36467679
|
C | G | 1 | a0001c0001t0006 | 2 | HG01167.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 125 | chr22 | 36467679 | |||||
chr22:36481597
|
T | C | 1 | a0001c0001t0013 | 1 | HG03491.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/4 | chr22 | 36481597 | ||||||
chr22:36481632
|
C | G | 1 | a0001c0001t0005 | 2 | HG02559.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-69G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/4 | 795 | chr22 | 36481632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:36468218
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0077 | 6 | HG00642.hp2 HG00741.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-301G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468218 | ||||||
chr22:36468320
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.388-403G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468320 | ||||||
chr22:36468324
|
C | G | 1 | a0001c0001t0003g0117 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.388-407G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468324 | ||||||
chr22:36468343
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.388-426G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468343 | ||||||
chr22:36468369
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.388-452T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468369 | ||||||
chr22:36468433
|
T | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(11): Show | 30 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-516A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468433 | ||||||
chr22:36468564
|
A | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0046others(10): Show | 27 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.388-647T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468564 | ||||||
chr22:36468570
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.388-653G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468570 | ||||||
chr22:36468640
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-723C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468640 | ||||||
chr22:36468644
|
G | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-727C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468644 | ||||||
chr22:36468720
|
CA | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-804delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468720 | ||||||
chr22:36468851
|
G | A | 1 | a0001c0001t0003g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.388-934C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468851 | ||||||
chr22:36468910
|
C | T | 1 | a0001c0001t0004g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.388-993G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468910 | ||||||
chr22:36469039
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.388-1122G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469039 | ||||||
chr22:36469041
|
C | CATAA | 11 | a0001c0001t0001g0091a0001c0001t0001g0144a0001c0001t0002g0004others(8): Show | 27 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.388-1128_388-1125d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | ||||||
chr22:36469041
|
C | CATAAATA others(1): Show |
3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0107 | 7 | HG01069.hp2 HG01071.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-1132_388-1125d others(10): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | ||||||
chr22:36469041
|
C | CATAAATA others(5): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0004t0001g0058 | 3 | NA18522.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-1136_388-1125d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | ||||||
chr22:36469061
|
AATAAATA others(5): Show |
A | 17 | a0001c0001t0003g0008a0001c0001t0003g0023a0001c0001t0003g0115others(14): Show | 31 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.388-1156_388-1145d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469061 | ||||||
chr22:36469069
|
A | AATAC | 16 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0043others(13): Show | 30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-1156_388-1153d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469069 | ||||||
chr22:36469069
|
AATAC | A | 2 | a0001c0001t0001g0009a0001c0001t0005g0021 | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-1156_388-1153d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469069 | ||||||
chr22:36469073
|
C | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0047others(8): Show | 21 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-1156G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469073 | ||||||
chr22:36469102
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0043others(13): Show | 30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-1185C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469102 | ||||||
chr22:36469105
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1188G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469105 | ||||||
chr22:36469112
|
C | T | 10 | a0001c0001t0003g0023a0001c0001t0003g0123a0001c0001t0004g0007others(7): Show | 18 | HG02572.hp2 HG02717.hp1 HG03209.hp2 others(15): Show |
intron_variant | MODIFIER | c.388-1195G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469112 | ||||||
chr22:36469133
|
G | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0043others(16): Show | 33 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.388-1216C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469133 | ||||||
chr22:36469140
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.388-1223G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469140 | ||||||
chr22:36469151
|
G | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0023a0001c0001t0003g0115others(15): Show | 32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-1234C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469151 | ||||||
chr22:36469172
|
C | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-1255G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469172 | ||||||
chr22:36469261
|
C | T | 7 | a0001c0001t0003g0123a0001c0001t0004g0007a0001c0001t0004g0125others(4): Show | 14 | HG03688.hp1 HG03834.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-1344G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469261 | ||||||
chr22:36469338
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1421T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469338 | ||||||
chr22:36469409
|
ACT | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(22): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.388-1494_388-1493d others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469409 | ||||||
chr22:36469550
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0068others(1): Show | 9 | HG00558.hp1 NA18944.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-1633A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469550 | ||||||
chr22:36469557
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1640A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469557 | ||||||
chr22:36469566
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1649A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469566 | ||||||
chr22:36469575
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1658G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469575 | ||||||
chr22:36469597
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1680A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469597 | ||||||
chr22:36469737
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.388-1820G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469737 | ||||||
chr22:36469749
|
A | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0023a0001c0001t0003g0115others(15): Show | 32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-1832T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469749 | ||||||
chr22:36469753
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.388-1836G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469753 | ||||||
chr22:36469785
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388-1868C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469785 | ||||||
chr22:36469815
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.388-1898C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469815 | ||||||
chr22:36469881
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-1964C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469881 | ||||||
chr22:36470054
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-2137T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470054 | ||||||
chr22:36470095
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2178G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470095 | ||||||
chr22:36470181
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.388-2264G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470181 | ||||||
chr22:36470230
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(49): Show | 97 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.388-2313G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470230 | ||||||
chr22:36470273
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2356G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470273 | ||||||
chr22:36470362
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0031others(20): Show | 47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.388-2445C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470362 | ||||||
chr22:36470451
|
A | G | 1 | a0001c0001t0003g0023 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.388-2534T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470451 | ||||||
chr22:36470560
|
TAAG | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2646_388-2644d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470560 | ||||||
chr22:36470567
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.388-2650A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470567 | ||||||
chr22:36470643
|
C | A | 1 | a0001c0001t0003g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.388-2726G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470643 | ||||||
chr22:36470660
|
C | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2743G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470660 | ||||||
chr22:36470684
|
C | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2767G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470684 | ||||||
chr22:36470761
|
C | T | 13 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0003g0023others(10): Show | 21 | HG02572.hp1 HG02572.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-2844G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470761 | ||||||
chr22:36470781
|
T | TAAA | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2867_388-2865d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470781 | ||||||
chr22:36470781
|
TA | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0001g0086others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-2865delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470781 | ||||||
chr22:36470885
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-2968G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470885 | ||||||
chr22:36470903
|
T | C | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-2986A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470903 | ||||||
chr22:36470932
|
A | T | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.388-3015T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470932 | ||||||
chr22:36470963
|
GCATACAC others(19): Show |
G | 2 | a0001c0001t0002g0107a0001c0001t0008g0030 | 3 | HG02135.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.388-3072_388-3047d others(28): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470963 | ||||||
chr22:36471049
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0047others(5): Show | 18 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.388-3132G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471049 | ||||||
chr22:36471063
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-3146G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471063 | ||||||
chr22:36471086
|
T | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0023a0001c0001t0003g0115others(15): Show | 32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-3169A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471086 | ||||||
chr22:36471182
|
TG | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0144others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-3266delC | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471182 | ||||||
chr22:36471317
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.388-3400C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471317 | ||||||
chr22:36471320
|
G | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0144others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-3403C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471320 | ||||||
chr22:36471399
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-3482A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471399 | ||||||
chr22:36471400
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-3483G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471400 | ||||||
chr22:36471417
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-3500G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471417 | ||||||
chr22:36471549
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.388-3632C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471549 | ||||||
chr22:36471623
|
C | G | 1 | a0001c0001t0002g0040 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.388-3706G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471623 | ||||||
chr22:36471689
|
A | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(28): Show | 61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-3772T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471689 | ||||||
chr22:36471705
|
CTGCCTGT others(1331): Show |
C | 1 | a0001c0001t0002g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.387+3690_388-3789d others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471705 | ||||||
chr22:36471708
|
C | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-3791G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471708 | ||||||
chr22:36471748
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0103 | 2 | NA18986.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.388-3831G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471748 | ||||||
chr22:36471771
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.388-3854G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471771 | ||||||
chr22:36471784
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(52): Show | 100 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.388-3867A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471784 | ||||||
chr22:36471812
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.388-3895A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471812 | ||||||
chr22:36471826
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02135.hp1 NA18980.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.388-3909G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471826 | ||||||
chr22:36471827
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.388-3910C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471827 | ||||||
chr22:36471842
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG00741.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-3925G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471842 | ||||||
chr22:36471843
|
G | A | 18 | a0001c0001t0003g0008a0001c0001t0003g0023a0001c0001t0003g0115others(15): Show | 32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-3926C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471843 | ||||||
chr22:36471892
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0022others(30): Show | 64 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.388-3975A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471892 | ||||||
chr22:36471895
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.388-3978C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471895 | ||||||
chr22:36471956
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(50): Show | 98 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.388-4039A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471956 | ||||||
chr22:36471968
|
T | TA | 23 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0062others(20): Show | 46 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.388-4052dupT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | ||||||
chr22:36471968
|
T | TAA | 11 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 19 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.388-4053_388-4052d others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | ||||||
chr22:36471968
|
T | TAAA | 8 | a0001c0001t0003g0123a0001c0001t0004g0007a0001c0001t0004g0124others(5): Show | 15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.388-4054_388-4052d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | ||||||
chr22:36471968
|
TA | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0076a0001c0001t0001g0108others(2): Show | 6 | HG02683.hp2 HG02895.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-4052delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | ||||||
chr22:36471976
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-4059T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471976 | ||||||
chr22:36471982
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.388-4065T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471982 | ||||||
chr22:36472057
|
CA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0056others(7): Show | 23 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-4141delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472057 | ||||||
chr22:36472123
|
G | A | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-4206C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472123 | ||||||
chr22:36472145
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-4228T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472145 | ||||||
chr22:36472213
|
G | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(32): Show | 66 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.388-4296C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472213 | ||||||
chr22:36472272
|
C | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-4355G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472272 | ||||||
chr22:36472519
|
C | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0031others(19): Show | 37 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+4214G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472519 | ||||||
chr22:36472588
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.387+4145G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472588 | ||||||
chr22:36472819
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.387+3914C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472819 | ||||||
chr22:36472822
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+3911G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472822 | ||||||
chr22:36472841
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3892A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472841 | ||||||
chr22:36472857
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.387+3876G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472857 | ||||||
chr22:36472874
|
GTCCGGGG others(21): Show |
G | 29 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(26): Show | 59 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.387+3831_387+3858d others(30): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472874 | ||||||
chr22:36472966
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.387+3767G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472966 | ||||||
chr22:36472992
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(93): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.387+3741A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472992 | ||||||
chr22:36473032
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.387+3701G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473032 | ||||||
chr22:36473046
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.387+3687G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473046 | ||||||
chr22:36473077
|
TGGGCGAA others(129): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387+3520_387+3655d others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473077 | ||||||
chr22:36473190
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0003g0023 | 3 | HG02572.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.387+3543G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473190 | ||||||
chr22:36473200
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.387+3533A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473200 | ||||||
chr22:36473304
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+3429C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473304 | ||||||
chr22:36473350
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.387+3383C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473350 | ||||||
chr22:36473365
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0056others(6): Show | 23 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.387+3368G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473365 | ||||||
chr22:36473422
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.387+3311C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473422 | ||||||
chr22:36473444
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0056others(5): Show | 21 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.387+3289T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473444 | ||||||
chr22:36473591
|
G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+3142C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473591 | ||||||
chr22:36473646
|
G | A | 1 | a0002c0004t0001g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+3087C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473646 | ||||||
chr22:36473668
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.387+3065T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473668 | ||||||
chr22:36473843
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.387+2890G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473843 | ||||||
chr22:36473848
|
G | A | 7 | a0001c0001t0003g0123a0001c0001t0004g0007a0001c0001t0004g0121others(4): Show | 14 | HG03209.hp2 HG03834.hp1 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+2885C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473848 | ||||||
chr22:36473880
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(9): Show | 27 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.387+2853C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473880 | ||||||
chr22:36473890
|
A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2843T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473890 | ||||||
chr22:36474051
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.387+2682G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474051 | ||||||
chr22:36474283
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(103): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.387+2450A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474283 | ||||||
chr22:36474420
|
T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2313A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474420 | ||||||
chr22:36474424
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(93): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.387+2309A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474424 | ||||||
chr22:36474457
|
T | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2276A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474457 | ||||||
chr22:36474498
|
T | G | 8 | a0001c0001t0003g0123a0001c0001t0004g0007a0001c0001t0004g0124others(5): Show | 15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+2235A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474498 | ||||||
chr22:36474535
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(9): Show | 27 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.387+2198G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474535 | ||||||
chr22:36474572
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2161G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474572 | ||||||
chr22:36474585
|
A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2148T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474585 | ||||||
chr22:36474740
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1993G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474740 | ||||||
chr22:36474749
|
C | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0003g0008others(5): Show | 14 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.387+1984G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474749 | ||||||
chr22:36474750
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.387+1983C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474750 | ||||||
chr22:36474774
|
A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1959T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474774 | ||||||
chr22:36474796
|
T | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0031others(44): Show | 90 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+1937A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474796 | ||||||
chr22:36474798
|
A | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0031others(44): Show | 90 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+1935T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474798 | ||||||
chr22:36474835
|
G | T | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+1898C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474835 | ||||||
chr22:36474906
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.387+1827G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474906 | ||||||
chr22:36474991
|
T | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1742A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474991 | ||||||
chr22:36475011
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387+1722A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475011 | ||||||
chr22:36475097
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+1636C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475097 | ||||||
chr22:36475115
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0005g0021 | 3 | HG02559.hp1 HG03098.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.387+1618G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475115 | ||||||
chr22:36475222
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1511T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475222 | ||||||
chr22:36475224
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1509T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475224 | ||||||
chr22:36475226
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1507T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475226 | ||||||
chr22:36475227
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1506T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475227 | ||||||
chr22:36475235
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1498G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475235 | ||||||
chr22:36475235
|
C | CG | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.387+1497dupC | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475235 | ||||||
chr22:36475236
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1497C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475236 | ||||||
chr22:36475237
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1496C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475237 | ||||||
chr22:36475238
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1495G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475238 | ||||||
chr22:36475239
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1494C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475239 | ||||||
chr22:36475241
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387+1492C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475241 | ||||||
chr22:36475242
|
GTGGCGCG others(5): Show |
G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1479_387+1490d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475242 | ||||||
chr22:36475261
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1472A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475261 | ||||||
chr22:36475262
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1471G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475262 | ||||||
chr22:36475265
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1468G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475265 | ||||||
chr22:36475267
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1466T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475267 | ||||||
chr22:36475269
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1464A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475269 | ||||||
chr22:36475270
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1463G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475270 | ||||||
chr22:36475271
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1462G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475271 | ||||||
chr22:36475273
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1460C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475273 | ||||||
chr22:36475274
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1459T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475274 | ||||||
chr22:36475275
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1458C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475275 | ||||||
chr22:36475276
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1457C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475276 | ||||||
chr22:36475277
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1456G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475277 | ||||||
chr22:36475277
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387+1456G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475277 | ||||||
chr22:36475278
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1455A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475278 | ||||||
chr22:36475279
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1454C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475279 | ||||||
chr22:36475286
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1447C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475286 | ||||||
chr22:36475291
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1442G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475291 | ||||||
chr22:36475293
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1440C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475293 | ||||||
chr22:36475294
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1439G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475294 | ||||||
chr22:36475304
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1429C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475304 | ||||||
chr22:36475308
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1425C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475308 | ||||||
chr22:36475309
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1424G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475309 | ||||||
chr22:36475314
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1419C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475314 | ||||||
chr22:36475320
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1413C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475320 | ||||||
chr22:36475323
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1410T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475323 | ||||||
chr22:36475324
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1409C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475324 | ||||||
chr22:36475325
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1408G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475325 | ||||||
chr22:36475327
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1406C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475327 | ||||||
chr22:36475333
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1400C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475333 | ||||||
chr22:36475336
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1397G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475336 | ||||||
chr22:36475337
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1396G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475337 | ||||||
chr22:36475339
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1394G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475339 | ||||||
chr22:36475341
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1392C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475341 | ||||||
chr22:36475342
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1391G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475342 | ||||||
chr22:36475344
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1389G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475344 | ||||||
chr22:36475346
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1387G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475346 | ||||||
chr22:36475347
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1386G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475347 | ||||||
chr22:36475349
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1384C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475349 | ||||||
chr22:36475353
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1380C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475353 | ||||||
chr22:36475355
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1378C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475355 | ||||||
chr22:36475359
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1374G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475359 | ||||||
chr22:36475362
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1371C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475362 | ||||||
chr22:36475363
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1370T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475363 | ||||||
chr22:36475366
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1367T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475366 | ||||||
chr22:36475370
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1363G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475370 | ||||||
chr22:36475378
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1355G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475378 | ||||||
chr22:36475380
|
A | ATCTAAAT others(3): Show |
1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1352_387+1353i others(12): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475380 | ||||||
chr22:36475386
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1347G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475386 | ||||||
chr22:36475389
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1344T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475389 | ||||||
chr22:36475392
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1341G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475392 | ||||||
chr22:36475393
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1340G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475393 | ||||||
chr22:36475394
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1339G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475394 | ||||||
chr22:36475395
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1338A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475395 | ||||||
chr22:36475396
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1337C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475396 | ||||||
chr22:36475398
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1335G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475398 | ||||||
chr22:36475399
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1334A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475399 | ||||||
chr22:36475405
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1328C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475405 | ||||||
chr22:36475409
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1324A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475409 | ||||||
chr22:36475412
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1321A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475412 | ||||||
chr22:36475417
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1316A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475417 | ||||||
chr22:36475418
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1315G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475418 | ||||||
chr22:36475419
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1314G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475419 | ||||||
chr22:36475420
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1313A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475420 | ||||||
chr22:36475422
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1311A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475422 | ||||||
chr22:36475433
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1300A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475433 | ||||||
chr22:36475524
|
A | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.387+1209T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475524 | ||||||
chr22:36475667
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0078a0001c0001t0001g0103others(1): Show | 5 | NA18947.hp2 NA18962.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1066A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475667 | ||||||
chr22:36475832
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.387+901G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475832 | ||||||
chr22:36475910
|
TTCTC | T | 1 | a0001c0001t0001g0009 | 6 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+819_387+822del others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475910 | ||||||
chr22:36475920
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387+813G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475920 | ||||||
chr22:36476067
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.387+666T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476067 | ||||||
chr22:36476211
|
C | T | 1 | a0001c0001t0001g0025 | 2 | NA18943.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.387+522G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476211 | ||||||
chr22:36476474
|
C | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+259G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476474 | ||||||
chr22:36476517
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.387+216C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476517 | ||||||
chr22:36476540
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.387+193G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476540 | ||||||
chr22:36476583
|
T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+150A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476583 | ||||||
chr22:36476587
|
G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+146C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476587 | ||||||
chr22:36476703
|
T | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(94): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.387+30A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476703 | ||||||
chr22:36476955
|
CTTA | C | 9 | a0001c0001t0003g0123a0001c0001t0004g0007a0001c0001t0004g0121others(6): Show | 16 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-102_264-100del others(3): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36476955 | ||||||
chr22:36477075
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.264-219G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477075 | ||||||
chr22:36477210
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-354G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477210 | ||||||
chr22:36477238
|
C | G | 29 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0060others(26): Show | 57 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.264-382G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477238 | ||||||
chr22:36477450
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.264-594G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477450 | ||||||
chr22:36477460
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.264-604C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477460 | ||||||
chr22:36477572
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.264-716T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477572 | ||||||
chr22:36477676
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.264-820G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477676 | ||||||
chr22:36477775
|
A | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-919T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477775 | ||||||
chr22:36477864
|
C | T | 29 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0060others(26): Show | 57 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.264-1008G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477864 | ||||||
chr22:36477920
|
T | C | 1 | a0001c0001t0004g0125 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264-1064A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477920 | ||||||
chr22:36477966
|
G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-1110C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477966 | ||||||
chr22:36477968
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-1112G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477968 | ||||||
chr22:36477976
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-1120T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477976 | ||||||
chr22:36477999
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.264-1143A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477999 | ||||||
chr22:36478132
|
C | CA | 35 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 67 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.264-1277dupT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | ||||||
chr22:36478132
|
C | CAAA | 6 | a0001c0001t0003g0008a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-1279_264-1277d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | ||||||
chr22:36478132
|
CA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0067others(7): Show | 24 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.264-1277delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | ||||||
chr22:36478176
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1320G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478176 | ||||||
chr22:36478463
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0003g0023 | 3 | HG02572.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.264-1607C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478463 | ||||||
chr22:36478495
|
CTTAT | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0142a0001c0005t0001g0147 | 4 | HG02486.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-1643_264-1640d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478495 | ||||||
chr22:36478552
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(37): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.264-1696G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478552 | ||||||
chr22:36478553
|
G | A | 7 | a0001c0001t0001g0143a0001c0001t0003g0008a0001c0001t0003g0115others(4): Show | 13 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-1697C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478553 | ||||||
chr22:36478630
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.264-1774A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478630 | ||||||
chr22:36478685
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.264-1829C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478685 | ||||||
chr22:36478733
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.263+1842G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478733 | ||||||
chr22:36478792
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.263+1783G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478792 | ||||||
chr22:36478803
|
C | G | 1 | a0001c0001t0003g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.263+1772G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478803 | ||||||
chr22:36478853
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.263+1722G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478853 | ||||||
chr22:36478880
|
G | A | 1 | a0001c0001t0003g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+1695C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478880 | ||||||
chr22:36478905
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0031others(43): Show | 89 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.263+1670G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478905 | ||||||
chr22:36478909
|
A | G | 30 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0060others(27): Show | 59 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.263+1666T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478909 | ||||||
chr22:36478974
|
C | A | 1 | a0001c0001t0004g0134 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.263+1601G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478974 | ||||||
chr22:36479081
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.263+1494G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479081 | ||||||
chr22:36479334
|
CT | C | 12 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0003g0123others(9): Show | 19 | HG01256.hp1 HG03209.hp2 HG03491.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1240delA | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479334 | ||||||
chr22:36479335
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.263+1240A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479335 | ||||||
chr22:36479392
|
C | T | 1 | a0002c0004t0001g0058 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.263+1183G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479392 | ||||||
chr22:36479395
|
G | A | 1 | a0001c0001t0002g0014 | 4 | NA18747.hp2 NA18950.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+1180C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479395 | ||||||
chr22:36479419
|
C | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0043others(13): Show | 30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1156G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479419 | ||||||
chr22:36479449
|
A | T | 1 | a0001c0001t0003g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+1126T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479449 | ||||||
chr22:36479583
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.263+992G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479583 | ||||||
chr22:36479622
|
G | C | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.263+953C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479622 | ||||||
chr22:36479624
|
G | A | 1 | a0001c0001t0003g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+951C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479624 | ||||||
chr22:36479864
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+711G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479864 | ||||||
chr22:36479865
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.263+710C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479865 | ||||||
chr22:36479882
|
CT | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0133a0001c0001t0001g0136others(2): Show | 7 | NA18948.hp2 NA18969.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+692delA | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479882 | ||||||
chr22:36479882
|
CTT | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0043others(12): Show | 30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+691_263+692del others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479882 | ||||||
chr22:36480009
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.263+566C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480009 | ||||||
chr22:36480041
|
G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+534C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480041 | ||||||
chr22:36480044
|
T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+531A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480044 | ||||||
chr22:36480071
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+504G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480071 | ||||||
chr22:36480118
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+457C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480118 | ||||||
chr22:36480315
|
T | C | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.263+260A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480315 | ||||||
chr22:36481011
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0045others(10): Show | 28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-174T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481011 | ||||||
chr22:36481058
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1-221G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481058 | ||||||
chr22:36481123
|
T | C | 1 | a0001c0001t0001g0032 | 2 | NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1-286A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481123 | ||||||
chr22:36481288
|
C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+276G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481288 | ||||||
chr22:36481412
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0002g0004a0001c0001t0002g0011others(9): Show | 31 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1+152T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481412 | ||||||
chr22:36481514
|
G | A | 1 | a0001c0001t0001g0020 | 3 | HG01070.hp1 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-1+50C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481514 | ||||||
chr22:36481550
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+14G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481550 |