geneid | 51061 |
---|---|
ensemblid | ENSG00000153066.13 |
hgncid | 28030 |
symbol | TXNDC11 |
name | thioredoxin domain containing 11 |
refseq_nuc | NM_015914.7 |
refseq_prot | NP_056998.4 |
ensembl_nuc | ENST00000283033.10 |
ensembl_prot | ENSP00000283033.5 |
mane_status | MANE Select |
chr | chr16 |
start | 11679083 |
end | 11742857 |
strand | - |
ver | v1.2 |
region | chr16:11679083-11742857 |
region5000 | chr16:11674083-11747857 |
regionname0 | TXNDC11_chr16_11679083_11742857 |
regionname5000 | TXNDC11_chr16_11674083_11747857 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 958 | 170 | 33 | 23 | 85 | 9 | 20 | 67 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002 | 1/0 | 958 | 96 | 36 | 15 | 32 | 2 | 10 | 24 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0003 | 0/1 | 958 | 84 | 1 | 23 | 42 | 6 | 11 | 29 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0004 | 0/0 | 958 | 6 | 0 | 0 | 5 | 0 | 1 | 5 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0005 | 0/0 | 958 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0006 | 0/0 | 958 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0007 | 0/0 | 958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0008 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0009 | 0/0 | 958 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0010 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0011 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0012 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0013 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0014 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0015 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0016 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0017 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2877 | 129 | 25 | 22 | 60 | 9 | 13 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0002 | 0/1 | 2877 | 84 | 1 | 23 | 42 | 6 | 11 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0003 | 1/0 | 2877 | 76 | 19 | 14 | 30 | 2 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0004 | 0/0 | 2877 | 28 | 2 | 0 | 19 | 0 | 7 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0005 | 0/0 | 2877 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0006 | 0/0 | 2877 | 6 | 0 | 0 | 5 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0007 | 0/0 | 2877 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0008 | 0/0 | 2877 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0009 | 0/0 | 2877 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0010 | 0/0 | 2877 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0011 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0012 | 0/0 | 2877 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0013 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0014 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0015 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0016 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0017 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0018 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0019 | 0/0 | 2877 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0020 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0021 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0022 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0023 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0024 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0025 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0026 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0027 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0028 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
c0029 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 240 | 369 | 78 | 62 | 168 | 18 | 41 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
t0002 | 0/0 | 240 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
t0003 | 0/0 | 240 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0297 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2877 | 129 | 25 | 22 | 60 | 9 | 13 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0004 | 0/0 | 2877 | 28 | 2 | 0 | 19 | 0 | 7 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0007 | 0/0 | 2877 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0008 | 0/0 | 2877 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0014 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0017 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0018 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0024 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0025 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0003 | 1/0 | 2877 | 76 | 19 | 14 | 30 | 2 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0005 | 0/0 | 2877 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0011 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0012 | 0/0 | 2877 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0023 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0003c0002 | 0/1 | 2877 | 84 | 1 | 23 | 42 | 6 | 11 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0004c0006 | 0/0 | 2877 | 6 | 0 | 0 | 5 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0005c0009 | 0/0 | 2877 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0006c0010 | 0/0 | 2877 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0007c0013 | 0/0 | 2877 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0008c0015 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0009c0019 | 0/0 | 2877 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0010c0026 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0011c0020 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0012c0021 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0013c0022 | 0/0 | 2877 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0014c0027 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0015c0016 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0016c0029 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0017c0028 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3116 | 129 | 25 | 22 | 60 | 9 | 13 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0004t0001 | 0/0 | 3116 | 28 | 2 | 0 | 19 | 0 | 7 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0007t0001 | 0/0 | 3116 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0008t0001 | 0/0 | 3116 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0014t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0017t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0018t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0024t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0001c0025t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0003t0001 | 1/0 | 3116 | 72 | 19 | 14 | 26 | 2 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0003t0002 | 0/0 | 3116 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0005t0001 | 0/0 | 3116 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0011t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0012t0001 | 0/0 | 3116 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0002c0023t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0003c0002t0001 | 0/1 | 3116 | 83 | 1 | 23 | 42 | 6 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0003c0002t0003 | 0/0 | 3116 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0004c0006t0001 | 0/0 | 3116 | 6 | 0 | 0 | 5 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0005c0009t0001 | 0/0 | 3116 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0006c0010t0001 | 0/0 | 3116 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0007c0013t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0008c0015t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0009c0019t0001 | 0/0 | 3116 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0010c0026t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0011c0020t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0012c0021t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0013c0022t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0014c0027t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0015c0016t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0016c0029t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
a0017c0028t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | copy fasta | chr16 | 11674083 | 11747857 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0007t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0014t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0014t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0017t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0018t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0024t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0001c0025t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0011t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0011t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0012t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0012t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0002c0023t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0297 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0003c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0004c0006t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0004c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0004c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0004c0006t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0005c0009t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0005c0009t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0005c0009t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0006c0010t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0006c0010t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0006c0010t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0007c0013t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0007c0013t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0008c0015t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0009c0019t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0010c0026t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0011c0020t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0012c0021t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0013c0022t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0014c0027t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0015c0016t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0016c0029t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
a0017c0028t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0002 | t0001 | g0335 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00099 | hp2 | a0009 | c0019 | t0001 | g0080 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00140 | hp1 | a0003 | c0002 | t0001 | g0311 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00140 | hp2 | a0003 | c0002 | t0001 | g0017 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00280 | hp1 | a0003 | c0002 | t0001 | g0016 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00323 | hp1 | a0003 | c0002 | t0001 | g0286 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00408 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0164 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0204 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00423 | hp2 | a0003 | c0002 | t0001 | g0321 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00544 | hp1 | a0001 | c0004 | t0001 | g0057 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00597 | hp1 | a0003 | c0002 | t0001 | g0347 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00621 | hp1 | a0008 | c0015 | t0001 | g0020 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0169 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00673 | hp1 | a0003 | c0002 | t0001 | g0330 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00733 | hp2 | a0003 | c0002 | t0001 | g0298 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00735 | hp1 | a0003 | c0002 | t0001 | g0312 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00735 | hp2 | a0003 | c0002 | t0001 | g0305 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0134 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01070 | hp1 | a0003 | c0002 | t0001 | g0352 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0148 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01074 | hp2 | a0003 | c0002 | t0001 | g0334 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01081 | hp2 | a0003 | c0002 | t0001 | g0290 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01099 | hp1 | a0003 | c0002 | t0001 | g0285 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0141 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01106 | hp1 | a0003 | c0002 | t0001 | g0017 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01106 | hp2 | a0003 | c0002 | t0001 | g0307 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0187 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01109 | hp2 | a0001 | c0007 | t0001 | g0004 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0143 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01168 | hp1 | a0003 | c0002 | t0001 | g0346 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01169 | hp2 | a0003 | c0002 | t0001 | g0291 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0183 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0191 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0150 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01255 | hp2 | a0003 | c0002 | t0001 | g0314 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01256 | hp2 | a0003 | c0002 | t0001 | g0316 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01261 | hp2 | a0002 | c0005 | t0001 | g0032 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01346 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01358 | hp2 | a0003 | c0002 | t0001 | g0300 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01361 | hp1 | a0003 | c0002 | t0001 | g0301 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01433 | hp2 | a0003 | c0002 | t0001 | g0348 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01496 | hp1 | a0005 | c0009 | t0001 | g0253 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0179 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0190 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01884 | hp2 | a0001 | c0007 | t0001 | g0023 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01891 | hp2 | a0002 | c0005 | t0001 | g0037 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01934 | hp1 | a0003 | c0002 | t0001 | g0317 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0151 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01952 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0193 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01978 | hp1 | a0003 | c0002 | t0001 | g0338 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01981 | hp1 | a0002 | c0003 | t0001 | g0199 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01981 | hp2 | a0003 | c0002 | t0001 | g0019 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0147 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02015 | hp1 | a0001 | c0004 | t0001 | g0045 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02015 | hp2 | a0003 | c0002 | t0001 | g0288 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02027 | hp1 | a0003 | c0002 | t0001 | g0280 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02055 | hp2 | a0002 | c0023 | t0001 | g0079 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02056 | hp2 | a0003 | c0002 | t0001 | g0344 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02080 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02083 | hp1 | a0003 | c0002 | t0001 | g0278 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0160 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02132 | hp2 | a0003 | c0002 | t0001 | g0018 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02135 | hp1 | a0003 | c0002 | t0001 | g0331 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0162 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02155 | hp2 | a0003 | c0002 | t0001 | g0339 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02165 | hp1 | a0001 | c0008 | t0001 | g0220 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02165 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0178 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0152 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02273 | hp2 | a0003 | c0002 | t0001 | g0327 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02523 | hp1 | a0003 | c0002 | t0001 | g0315 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02572 | hp2 | a0001 | c0007 | t0001 | g0004 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02615 | hp2 | a0006 | c0010 | t0001 | g0273 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02622 | hp1 | a0001 | c0014 | t0001 | g0068 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0136 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02717 | hp2 | a0002 | c0005 | t0001 | g0038 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02723 | hp1 | a0002 | c0005 | t0001 | g0039 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0137 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02738 | hp1 | a0003 | c0002 | t0001 | g0349 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0197 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02809 | hp1 | a0005 | c0009 | t0001 | g0223 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0140 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02818 | hp1 | a0002 | c0005 | t0001 | g0034 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02886 | hp1 | a0002 | c0005 | t0001 | g0005 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0189 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02895 | hp1 | a0002 | c0005 | t0001 | g0029 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02896 | hp1 | a0005 | c0009 | t0001 | g0250 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02896 | hp2 | a0002 | c0005 | t0001 | g0033 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02922 | hp1 | a0002 | c0005 | t0001 | g0028 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0114 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0133 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0061 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03017 | hp2 | a0002 | c0003 | t0001 | g0138 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03041 | hp1 | a0006 | c0010 | t0001 | g0272 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03041 | hp2 | a0002 | c0003 | t0001 | g0161 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03098 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0180 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03130 | hp2 | a0002 | c0005 | t0001 | g0005 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03195 | hp2 | a0002 | c0005 | t0001 | g0036 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0130 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0177 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03225 | hp2 | a0002 | c0005 | t0001 | g0027 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0052 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03453 | hp2 | a0002 | c0005 | t0001 | g0035 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0131 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03486 | hp2 | a0007 | c0013 | t0001 | g0113 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03490 | hp2 | a0002 | c0003 | t0001 | g0135 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03491 | hp1 | a0003 | c0002 | t0003 | g0296 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0054 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03492 | hp2 | a0003 | c0002 | t0001 | g0293 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03516 | hp1 | a0007 | c0013 | t0001 | g0112 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03516 | hp2 | a0002 | c0005 | t0001 | g0030 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03540 | hp1 | a0002 | c0011 | t0001 | g0063 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03654 | hp1 | a0002 | c0003 | t0001 | g0186 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03669 | hp1 | a0003 | c0002 | t0001 | g0306 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03688 | hp1 | a0003 | c0002 | t0001 | g0322 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0201 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03704 | hp2 | a0003 | c0002 | t0001 | g0295 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0053 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0200 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03834 | hp1 | a0003 | c0002 | t0001 | g0303 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0043 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03927 | hp1 | a0001 | c0004 | t0001 | g0060 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03927 | hp2 | a0003 | c0002 | t0001 | g0287 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04115 | hp1 | a0003 | c0002 | t0001 | g0313 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0139 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04204 | hp2 | a0003 | c0002 | t0001 | g0016 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0046 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG04228 | hp2 | a0003 | c0002 | t0001 | g0304 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0175 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18522 | hp2 | a0002 | c0011 | t0001 | g0062 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18612 | hp1 | a0003 | c0002 | t0001 | g0328 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0158 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18747 | hp2 | a0003 | c0002 | t0001 | g0340 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18906 | hp1 | a0006 | c0010 | t0001 | g0274 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18940 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18940 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18941 | hp1 | a0003 | c0002 | t0001 | g0308 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18941 | hp2 | a0017 | c0028 | t0001 | g0275 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18942 | hp2 | a0003 | c0002 | t0001 | g0323 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18946 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18946 | hp2 | a0003 | c0002 | t0001 | g0324 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18947 | hp1 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18947 | hp2 | a0003 | c0002 | t0001 | g0337 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18948 | hp1 | a0003 | c0002 | t0001 | g0284 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18948 | hp2 | a0012 | c0021 | t0001 | g0154 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18949 | hp2 | a0001 | c0017 | t0001 | g0042 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18951 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18951 | hp2 | a0002 | c0012 | t0001 | g0167 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18952 | hp1 | a0003 | c0002 | t0001 | g0309 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18953 | hp2 | a0004 | c0006 | t0001 | g0351 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18954 | hp1 | a0003 | c0002 | t0001 | g0343 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18954 | hp2 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18957 | hp2 | a0003 | c0002 | t0001 | g0329 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18961 | hp2 | a0003 | c0002 | t0001 | g0342 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18965 | hp2 | a0003 | c0002 | t0001 | g0325 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18966 | hp2 | a0003 | c0002 | t0001 | g0019 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18970 | hp2 | a0001 | c0004 | t0001 | g0050 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18972 | hp1 | a0003 | c0002 | t0001 | g0333 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18973 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18973 | hp2 | a0003 | c0002 | t0001 | g0318 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18975 | hp2 | a0003 | c0002 | t0001 | g0292 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18978 | hp1 | a0003 | c0002 | t0001 | g0279 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18979 | hp1 | a0011 | c0020 | t0001 | g0085 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18982 | hp1 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18984 | hp2 | a0003 | c0002 | t0001 | g0341 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0168 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18986 | hp1 | a0004 | c0006 | t0001 | g0294 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18986 | hp2 | a0001 | c0008 | t0001 | g0219 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18988 | hp2 | a0003 | c0002 | t0001 | g0281 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18991 | hp1 | a0003 | c0002 | t0001 | g0350 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18991 | hp2 | a0001 | c0004 | t0001 | g0048 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18994 | hp1 | a0003 | c0002 | t0001 | g0310 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18994 | hp2 | a0014 | c0027 | t0001 | g0270 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18999 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19002 | hp1 | a0003 | c0002 | t0001 | g0319 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19003 | hp2 | a0003 | c0002 | t0001 | g0276 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19009 | hp1 | a0003 | c0002 | t0001 | g0277 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19010 | hp2 | a0002 | c0012 | t0001 | g0156 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19011 | hp1 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0157 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19012 | hp1 | a0003 | c0002 | t0001 | g0283 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19030 | hp1 | a0001 | c0018 | t0001 | g0024 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19030 | hp2 | a0002 | c0003 | t0001 | g0182 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0181 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19043 | hp2 | a0013 | c0022 | t0001 | g0165 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19054 | hp1 | a0003 | c0002 | t0001 | g0002 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19057 | hp2 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19058 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19064 | hp2 | a0003 | c0002 | t0001 | g0320 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19066 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19075 | hp2 | a0001 | c0024 | t0001 | g0071 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19079 | hp1 | a0001 | c0008 | t0001 | g0247 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19079 | hp2 | a0001 | c0025 | t0001 | g0100 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19080 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19081 | hp1 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19081 | hp2 | a0001 | c0004 | t0001 | g0055 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19082 | hp2 | a0001 | c0004 | t0001 | g0051 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19084 | hp1 | a0010 | c0026 | t0001 | g0265 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19084 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19085 | hp1 | a0015 | c0016 | t0001 | g0021 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19085 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19086 | hp1 | a0003 | c0002 | t0001 | g0289 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19088 | hp1 | a0003 | c0002 | t0001 | g0282 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19089 | hp2 | a0003 | c0002 | t0001 | g0332 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19090 | hp1 | a0016 | c0029 | t0001 | g0345 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ASW | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20129 | hp2 | a0001 | c0014 | t0001 | g0117 | AFR | ASW | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0185 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0188 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20805 | hp1 | a0003 | c0002 | t0001 | g0336 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20905 | hp2 | a0004 | c0006 | t0001 | g0299 | SAS | GIH | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01123 | hp1 | a0003 | c0002 | t0001 | g0018 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02109 | hp1 | a0002 | c0003 | t0001 | g0176 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0173 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0132 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02559 | hp1 | a0002 | c0005 | t0001 | g0031 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG02559 | hp2 | a0001 | c0007 | t0001 | g0022 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA18955 | hp2 | a0003 | c0002 | t0001 | g0326 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
NA20300 | hp2 | a0003 | c0002 | t0001 | g0302 | AFR | USA | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
homoSapiens_chm13v2 | hp1 | a0003 | c0002 | t0001 | g0297 | REF | REF | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0155 | REF | REF | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:11679679
|
C | G | 1 | a0007 | 2 | HG03486.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2393G>C | p.Gly798Ala | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2520/3116 | 2393/2877 | 798/958 | chr16 | 11679679 | ||
chr16:11679806
|
C | G | 8 | a0001a0004a0005others(5): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
missense_variant | MODERATE | c.2266G>C | p.Val756Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2393/3116 | 2266/2877 | 756/958 | chr16 | 11679806 | ||
chr16:11687885
|
G | C | 1 | a0005 | 3 | HG01496.hp1 HG02809.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.2125C>G | p.Leu709Val | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2252/3116 | 2125/2877 | 709/958 | chr16 | 11687885 | ||
chr16:11698246
|
C | T | 1 | a0013 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.986G>A | p.Arg329Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1113/3116 | 986/2877 | 329/958 | chr16 | 11698246 | ||
chr16:11698315
|
C | T | 2 | a0012a0016 | 2 | NA18948.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.917G>A | p.Arg306Lys | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1044/3116 | 917/2877 | 306/958 | chr16 | 11698315 | ||
chr16:11700546
|
C | T | 1 | a0011 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/12 | 939/3116 | 812/2877 | 271/958 | chr16 | 11700546 | ||
chr16:11721634
|
G | T | 1 | a0017 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.736C>A | p.Pro246Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/12 | 863/3116 | 736/2877 | 246/958 | chr16 | 11721634 | ||
chr16:11730653
|
T | C | 1 | a0010 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.691A>G | p.Asn231Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/12 | 818/3116 | 691/2877 | 231/958 | chr16 | 11730653 | ||
chr16:11730713
|
G | A | 1 | a0014 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.631C>T | p.Arg211Trp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/12 | 758/3116 | 631/2877 | 211/958 | chr16 | 11730713 | ||
chr16:11736030
|
C | T | 1 | a0009 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.458G>A | p.Arg153Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/12 | 585/3116 | 458/2877 | 153/958 | chr16 | 11736030 | ||
chr16:11742493
|
G | C | 1 | a0006 | 3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.238C>G | p.Leu80Val | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 365/3116 | 238/2877 | 80/958 | chr16 | 11742493 | ||
chr16:11742630
|
C | G | 1 | a0015 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.101G>C | p.Ser34Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 228/3116 | 101/2877 | 34/958 | chr16 | 11742630 | ||
chr16:11742652
|
G | A | 4 | a0003a0004a0016others(1): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
missense_variant | MODERATE | c.79C>T | p.Pro27Ser | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 206/3116 | 79/2877 | 27/958 | chr16 | 11742652 | ||
chr16:11742714
|
C | T | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.17G>A | p.Gly6Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 144/3116 | 17/2877 | 6/958 | chr16 | 11742714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:11679405
|
G | C | 2 | a0002c0011a0002c0023 | 3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2667C>G | p.Thr889Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2794/3116 | 2667/2877 | 889/958 | chr16 | 11679405 | ||
chr16:11687934
|
G | A | 1 | a0001c0014 | 2 | HG02622.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.2076C>T | p.Cys692Cys | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2203/3116 | 2076/2877 | 692/958 | chr16 | 11687934 | ||
chr16:11687946
|
G | A | 1 | a0001c0007 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.2064C>T | p.Tyr688Tyr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2191/3116 | 2064/2877 | 688/958 | chr16 | 11687946 | ||
chr16:11691771
|
A | G | 1 | a0001c0008 | 3 | HG02165.hp1 NA18986.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.1419T>C | p.Asp473Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1546/3116 | 1419/2877 | 473/958 | chr16 | 11691771 | ||
chr16:11691870
|
G | A | 1 | a0001c0017 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1320C>T | p.Asn440Asn | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1447/3116 | 1320/2877 | 440/958 | chr16 | 11691870 | ||
chr16:11692047
|
A | G | 1 | a0002c0012 | 2 | NA18951.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.1143T>C | p.His381His | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1270/3116 | 1143/2877 | 381/958 | chr16 | 11692047 | ||
chr16:11698128
|
G | A | 1 | a0001c0018 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1104C>T | p.Asp368Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1231/3116 | 1104/2877 | 368/958 | chr16 | 11698128 | ||
chr16:11698154
|
G | A | 1 | a0001c0024 | 1 | NA19075.hp2 | synonymous_variant | LOW | c.1078C>T | p.Leu360Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1205/3116 | 1078/2877 | 360/958 | chr16 | 11698154 | ||
chr16:11698269
|
T | C | 1 | a0001c0025 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.963A>G | p.Leu321Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1090/3116 | 963/2877 | 321/958 | chr16 | 11698269 | ||
chr16:11742542
|
C | G | 10 | a0001c0004a0001c0007a0001c0017others(7): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
synonymous_variant | LOW | c.189G>C | p.Pro63Pro | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 316/3116 | 189/2877 | 63/958 | chr16 | 11742542 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:11679131
|
A | T | 1 | a0003c0002t0003 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 64 | chr16 | 11679131 | |||||
chr16:11679191
|
A | C | 1 | a0002c0003t0002 | 4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 4 | chr16 | 11679191 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:11679877
|
C | G | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(39): Show | 46 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2235-40G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679877 | ||||||
chr16:11679887
|
G | T | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2235-50C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679887 | ||||||
chr16:11679944
|
C | T | 1 | a0001c0017t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2235-107G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679944 | ||||||
chr16:11679945
|
G | A | 8 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(5): Show | 8 | HG02074.hp1 NA18961.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.2235-108C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679945 | ||||||
chr16:11679950
|
G | A | 19 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(16): Show | 20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.2235-113C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679950 | ||||||
chr16:11680029
|
T | A | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2235-192A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680029 | ||||||
chr16:11680125
|
A | G | 26 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(23): Show | 29 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.2235-288T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680125 | ||||||
chr16:11680345
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 74 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.2235-508C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680345 | ||||||
chr16:11680503
|
G | C | 1 | a0003c0002t0003g0296 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2235-666C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680503 | ||||||
chr16:11680527
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2235-690C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680527 | ||||||
chr16:11680724
|
C | G | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2235-887G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680724 | ||||||
chr16:11680769
|
C | T | 102 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2235-932G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680769 | ||||||
chr16:11680773
|
C | T | 1 | a0003c0002t0001g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2235-936G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680773 | ||||||
chr16:11680774
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2235-937C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680774 | ||||||
chr16:11680920
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2235-1083C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680920 | ||||||
chr16:11680975
|
T | C | 2 | a0003c0002t0001g0319a0003c0002t0001g0326 | 2 | NA18955.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2235-1138A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680975 | ||||||
chr16:11681019
|
A | C | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2235-1182T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681019 | ||||||
chr16:11681094
|
T | C | 118 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2235-1257A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681094 | ||||||
chr16:11681203
|
C | G | 1 | a0003c0002t0001g0350 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2235-1366G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681203 | ||||||
chr16:11681344
|
C | G | 1 | a0002c0005t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2235-1507G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681344 | ||||||
chr16:11681388
|
G | A | 1 | a0003c0002t0001g0324 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2235-1551C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681388 | ||||||
chr16:11681644
|
C | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2235-1807G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681644 | ||||||
chr16:11681964
|
A | G | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2235-2127T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681964 | ||||||
chr16:11682016
|
T | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2234+2149A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682016 | ||||||
chr16:11682651
|
C | T | 1 | a0003c0002t0001g0314 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2234+1514G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682651 | ||||||
chr16:11682652
|
G | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2234+1513C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682652 | ||||||
chr16:11682969
|
A | G | 10 | a0002c0003t0001g0142a0002c0003t0001g0157a0002c0003t0001g0158others(7): Show | 10 | HG02132.hp1 HG02155.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.2234+1196T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682969 | ||||||
chr16:11682982
|
A | C | 2 | a0003c0002t0001g0319a0003c0002t0001g0326 | 2 | NA18955.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2234+1183T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682982 | ||||||
chr16:11682983
|
C | T | 1 | a0002c0003t0001g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2234+1182G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682983 | ||||||
chr16:11683107
|
G | C | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2234+1058C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683107 | ||||||
chr16:11683169
|
C | A | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2234+996G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683169 | ||||||
chr16:11683196
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2234+969G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683196 | ||||||
chr16:11683254
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2234+911C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683254 | ||||||
chr16:11683368
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2234+797G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683368 | ||||||
chr16:11683523
|
T | C | 1 | a0002c0003t0001g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2234+642A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683523 | ||||||
chr16:11683571
|
CAGA | C | 103 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2234+591_2234+593d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683571 | ||||||
chr16:11683596
|
T | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2234+569A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683596 | ||||||
chr16:11683639
|
C | T | 1 | a0002c0003t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2234+526G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683639 | ||||||
chr16:11683649
|
C | G | 2 | a0012c0021t0001g0154a0016c0029t0001g0345 | 2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2234+516G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683649 | ||||||
chr16:11683748
|
C | CT | 31 | a0001c0001t0001g0115a0002c0003t0001g0129a0002c0003t0001g0130others(28): Show | 32 | HG01192.hp1 HG01261.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.2234+416dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683748 | ||||||
chr16:11683748
|
CT | C | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2234+416delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683748 | ||||||
chr16:11683782
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0124a0001c0001t0001g0126 | 4 | HG01167.hp2 HG01169.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2234+383G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683782 | ||||||
chr16:11683826
|
A | C | 1 | a0002c0003t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2234+339T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683826 | ||||||
chr16:11684069
|
G | A | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2234+96C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11684069 | ||||||
chr16:11684371
|
T | A | 1 | a0003c0002t0001g0298 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2154-126A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684371 | ||||||
chr16:11684515
|
G | A | 2 | a0003c0002t0001g0311a0003c0002t0001g0312 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2154-270C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684515 | ||||||
chr16:11684669
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2154-424T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684669 | ||||||
chr16:11684671
|
CA | C | 101 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2154-427delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684671 | ||||||
chr16:11684778
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 11 | NA18940.hp1 NA18942.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2154-533C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684778 | ||||||
chr16:11684836
|
C | T | 1 | a0001c0004t0001g0041 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2154-591G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684836 | ||||||
chr16:11684982
|
G | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2154-737C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684982 | ||||||
chr16:11685015
|
G | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0210a0001c0001t0001g0228others(1): Show | 5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-770C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685015 | ||||||
chr16:11685207
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154-962A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685207 | ||||||
chr16:11685304
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154-1059A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685304 | ||||||
chr16:11685324
|
C | T | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2154-1079G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685324 | ||||||
chr16:11685334
|
G | C | 1 | a0003c0002t0001g0327 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2154-1089C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685334 | ||||||
chr16:11685385
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 63 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2154-1140A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685385 | ||||||
chr16:11685392
|
T | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2154-1147A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685392 | ||||||
chr16:11685425
|
C | T | 1 | a0003c0002t0001g0352 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2154-1180G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685425 | ||||||
chr16:11685462
|
G | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(94): Show | 104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2154-1217C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685462 | ||||||
chr16:11685469
|
C | T | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(39): Show | 46 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2154-1224G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685469 | ||||||
chr16:11685475
|
C | A | 22 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(19): Show | 25 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.2154-1230G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685475 | ||||||
chr16:11685581
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2154-1336C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685581 | ||||||
chr16:11685653
|
A | C | 103 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2154-1408T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685653 | ||||||
chr16:11685715
|
C | T | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2154-1470G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685715 | ||||||
chr16:11685717
|
A | C | 1 | a0001c0001t0001g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2154-1472T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685717 | ||||||
chr16:11685873
|
T | C | 1 | a0003c0002t0001g0339 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2154-1628A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685873 | ||||||
chr16:11685913
|
A | C | 1 | a0002c0003t0001g0185 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2154-1668T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685913 | ||||||
chr16:11685953
|
C | G | 6 | a0002c0003t0001g0141a0002c0003t0001g0147a0002c0003t0001g0151others(3): Show | 6 | HG01099.hp2 HG01192.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-1708G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685953 | ||||||
chr16:11686075
|
C | T | 1 | a0003c0002t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2153+1782G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686075 | ||||||
chr16:11686654
|
A | G | 2 | a0001c0001t0001g0153a0004c0006t0001g0294 | 2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2153+1203T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686654 | ||||||
chr16:11686690
|
T | G | 1 | a0007c0013t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2153+1167A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686690 | ||||||
chr16:11686773
|
G | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.2153+1084C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686773 | ||||||
chr16:11686799
|
T | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+1058A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686799 | ||||||
chr16:11686806
|
C | G | 1 | a0002c0003t0001g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2153+1051G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686806 | ||||||
chr16:11686812
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2153+1045C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686812 | ||||||
chr16:11686818
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+1039T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686818 | ||||||
chr16:11686859
|
T | C | 3 | a0002c0011t0001g0062a0002c0011t0001g0063a0002c0023t0001g0079 | 3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2153+998A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686859 | ||||||
chr16:11686918
|
T | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.2153+939A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686918 | ||||||
chr16:11686957
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0104others(1): Show | 5 | HG00609.hp2 HG02135.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+900C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686957 | ||||||
chr16:11686983
|
G | A | 6 | a0001c0001t0001g0227a0001c0001t0001g0240a0001c0001t0001g0254others(3): Show | 6 | HG00609.hp1 HG02083.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2153+874C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686983 | ||||||
chr16:11687024
|
G | C | 1 | a0003c0002t0001g0327 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2153+833C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687024 | ||||||
chr16:11687103
|
C | G | 3 | a0002c0003t0001g0142a0002c0003t0001g0170a0002c0003t0001g0171 | 3 | NA18990.hp2 NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2153+754G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687103 | ||||||
chr16:11687356
|
CCTT | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 65 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.2153+498_2153+500d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687356 | ||||||
chr16:11687395
|
C | A | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2153+462G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687395 | ||||||
chr16:11687404
|
G | A | 103 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2153+453C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687404 | ||||||
chr16:11687444
|
A | G | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2153+413T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687444 | ||||||
chr16:11687505
|
C | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+352G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687505 | ||||||
chr16:11687598
|
C | T | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2153+259G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687598 | ||||||
chr16:11687726
|
A | C | 101 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2153+131T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687726 | ||||||
chr16:11687759
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(10): Show | 14 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2153+98A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687759 | ||||||
chr16:11687835
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+22C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687835 | ||||||
chr16:11687839
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2153+18G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687839 | ||||||
chr16:11688162
|
A | C | 1 | a0002c0003t0001g0187 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2043+141T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 9/11 | chr16 | 11688162 | ||||||
chr16:11688193
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(11): Show | 15 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2043+110C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 9/11 | chr16 | 11688193 | ||||||
chr16:11688468
|
A | T | 1 | a0003c0002t0001g0316 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1901-23T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688468 | ||||||
chr16:11688501
|
G | A | 1 | a0012c0021t0001g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1901-56C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688501 | ||||||
chr16:11688671
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1901-226T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688671 | ||||||
chr16:11688729
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1901-284A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688729 | ||||||
chr16:11688799
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0108 | 2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1901-354G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688799 | ||||||
chr16:11688944
|
G | A | 6 | a0002c0003t0001g0011a0002c0003t0001g0144a0002c0003t0001g0146others(3): Show | 7 | NA18939.hp2 NA18959.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1901-499C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688944 | ||||||
chr16:11689075
|
A | T | 2 | a0002c0005t0001g0005a0002c0005t0001g0035 | 3 | HG02886.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1901-630T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689075 | ||||||
chr16:11689087
|
C | CT | 10 | a0001c0001t0001g0224a0002c0003t0001g0129a0002c0003t0001g0130others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1901-643dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689087
|
C | CTT | 92 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(89): Show | 100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1901-644_1901-643d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689087
|
C | CTTT | 11 | a0001c0001t0001g0122a0001c0001t0001g0209a0001c0001t0001g0211others(8): Show | 11 | HG01175.hp2 HG02165.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1901-645_1901-643d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689087
|
C | CTTTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0097a0001c0001t0001g0109others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1901-646_1901-643d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689087
|
C | CTTTTT | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 56 | HG00609.hp2 HG00741.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1901-647_1901-643d others(7): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689087
|
C | CTTTTTT | 6 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0271others(3): Show | 6 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901-648_1901-643d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | ||||||
chr16:11689104
|
A | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1901-659T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689104 | ||||||
chr16:11689206
|
A | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-761T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689206 | ||||||
chr16:11689234
|
G | A | 2 | a0012c0021t0001g0154a0016c0029t0001g0345 | 2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1901-789C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689234 | ||||||
chr16:11689242
|
T | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-797A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689242 | ||||||
chr16:11689260
|
T | C | 1 | a0002c0003t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1901-815A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689260 | ||||||
chr16:11689372
|
T | C | 1 | a0003c0002t0001g0328 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1901-927A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689372 | ||||||
chr16:11689467
|
A | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-1022T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689467 | ||||||
chr16:11689471
|
T | C | 2 | a0003c0002t0001g0330a0003c0002t0001g0331 | 2 | HG00673.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1901-1026A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689471 | ||||||
chr16:11689616
|
A | G | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1901-1171T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689616 | ||||||
chr16:11689746
|
T | C | 1 | a0003c0002t0001g0340 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1901-1301A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689746 | ||||||
chr16:11689767
|
C | T | 2 | a0001c0001t0001g0153a0004c0006t0001g0294 | 2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1901-1322G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689767 | ||||||
chr16:11689794
|
A | T | 2 | a0001c0014t0001g0068a0001c0014t0001g0117 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1901-1349T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689794 | ||||||
chr16:11689868
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1422T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689868 | ||||||
chr16:11689880
|
C | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1410G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689880 | ||||||
chr16:11689881
|
G | A | 1 | a0002c0003t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1900+1409C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689881 | ||||||
chr16:11689907
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1383T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689907 | ||||||
chr16:11689908
|
C | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1382G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689908 | ||||||
chr16:11689913
|
C | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1377G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689913 | ||||||
chr16:11689925
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1365A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689925 | ||||||
chr16:11689926
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1364A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689926 | ||||||
chr16:11689928
|
C | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1362G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689928 | ||||||
chr16:11689929
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1361T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689929 | ||||||
chr16:11689930
|
C | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1360G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689930 | ||||||
chr16:11689935
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1355T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689935 | ||||||
chr16:11689940
|
C | A | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1350G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689940 | ||||||
chr16:11689948
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1342A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689948 | ||||||
chr16:11689949
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1341A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689949 | ||||||
chr16:11689950
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1340A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689950 | ||||||
chr16:11689960
|
A | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1330T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689960 | ||||||
chr16:11689970
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1320T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689970 | ||||||
chr16:11689972
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1318T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689972 | ||||||
chr16:11689975
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1315T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689975 | ||||||
chr16:11689976
|
A | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1314T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689976 | ||||||
chr16:11689978
|
C | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1312G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689978 | ||||||
chr16:11689983
|
T | A | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1307A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689983 | ||||||
chr16:11689986
|
A | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1304T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689986 | ||||||
chr16:11689987
|
C | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1303G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689987 | ||||||
chr16:11689988
|
A | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1302T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689988 | ||||||
chr16:11689994
|
C | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1296G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689994 | ||||||
chr16:11690025
|
A | C | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1265T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690025 | ||||||
chr16:11690065
|
C | A | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1225G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690065 | ||||||
chr16:11690067
|
T | G | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1223A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690067 | ||||||
chr16:11690082
|
A | C | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1208T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690082 | ||||||
chr16:11690090
|
G | A | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1900+1200C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690090 | ||||||
chr16:11690177
|
C | T | 1 | a0003c0002t0001g0343 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1900+1113G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690177 | ||||||
chr16:11690187
|
C | A | 1 | a0003c0002t0001g0350 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1900+1103G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690187 | ||||||
chr16:11690189
|
A | T | 1 | a0003c0002t0001g0350 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1900+1101T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690189 | ||||||
chr16:11690213
|
T | C | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900+1077A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690213 | ||||||
chr16:11690273
|
G | T | 171 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 185 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1900+1017C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690273 | ||||||
chr16:11690473
|
A | T | 19 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(16): Show | 20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1900+817T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690473 | ||||||
chr16:11690498
|
A | G | 3 | a0002c0011t0001g0062a0002c0011t0001g0063a0002c0023t0001g0079 | 3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1900+792T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690498 | ||||||
chr16:11690610
|
G | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1900+680C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690610 | ||||||
chr16:11690661
|
T | G | 1 | a0003c0002t0001g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1900+629A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690661 | ||||||
chr16:11690708
|
G | A | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1900+582C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690708 | ||||||
chr16:11690719
|
A | AT | 5 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(2): Show | 6 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1900+570dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690719 | ||||||
chr16:11690821
|
A | G | 1 | a0001c0004t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1900+469T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690821 | ||||||
chr16:11691011
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121 | 3 | HG03654.hp2 HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1900+279A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691011 | ||||||
chr16:11691024
|
G | A | 101 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1900+266C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691024 | ||||||
chr16:11691081
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0108 | 2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1900+209T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691081 | ||||||
chr16:11691109
|
C | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1900+181G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691109 | ||||||
chr16:11692233
|
G | A | 1 | a0002c0005t0001g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1108-151C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692233 | ||||||
chr16:11692241
|
T | TA | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-160dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692241 | ||||||
chr16:11692548
|
A | T | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1108-466T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692548 | ||||||
chr16:11692579
|
T | C | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1108-497A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692579 | ||||||
chr16:11692611
|
G | A | 1 | a0001c0004t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1108-529C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692611 | ||||||
chr16:11692691
|
C | T | 2 | a0003c0002t0001g0308a0003c0002t0001g0310 | 2 | NA18941.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1108-609G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692691 | ||||||
chr16:11692697
|
A | G | 136 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1108-615T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692697 | ||||||
chr16:11692766
|
C | G | 2 | a0001c0001t0001g0153a0004c0006t0001g0294 | 2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1108-684G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692766 | ||||||
chr16:11692766
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0210a0001c0001t0001g0228others(1): Show | 5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-684G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692766 | ||||||
chr16:11692911
|
G | A | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-829C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692911 | ||||||
chr16:11693153
|
A | G | 1 | a0001c0004t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1108-1071T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693153 | ||||||
chr16:11693200
|
A | G | 3 | a0002c0003t0001g0138a0002c0003t0001g0185a0002c0003t0001g0187 | 3 | HG01109.hp1 HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1108-1118T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693200 | ||||||
chr16:11693308
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1108-1226G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693308 | ||||||
chr16:11693463
|
G | A | 1 | a0003c0002t0001g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1108-1381C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693463 | ||||||
chr16:11693568
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0228 | 2 | HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1108-1486G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693568 | ||||||
chr16:11693685
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1108-1603T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693685 | ||||||
chr16:11693833
|
C | A | 100 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(97): Show | 107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1108-1751G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693833 | ||||||
chr16:11693858
|
G | C | 185 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 199 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1108-1776C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693858 | ||||||
chr16:11693892
|
C | G | 1 | a0003c0002t0001g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1108-1810G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693892 | ||||||
chr16:11694051
|
G | A | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1108-1969C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694051 | ||||||
chr16:11694097
|
C | CT | 54 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0001t0001g0122others(51): Show | 57 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1108-2016dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
C | CTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0123others(7): Show | 11 | HG01167.hp2 HG01175.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-2017_1108-201 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CT | C | 7 | a0002c0003t0001g0163a0002c0003t0001g0192a0002c0003t0001g0196others(4): Show | 7 | HG01070.hp1 HG01168.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-2016delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0231others(4): Show | 7 | HG02027.hp1 NA18522.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-2022_1108-201 others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT others(1): Show |
C | 87 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1108-2023_1108-201 others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1108-2025_1108-201 others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT others(4): Show |
C | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(36): Show | 43 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1108-2026_1108-201 others(15): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(12): Show | 16 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1108-2027_1108-201 others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694097
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1108-2029_1108-201 others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | ||||||
chr16:11694234
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1108-2152G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694234 | ||||||
chr16:11694236
|
G | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 166 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1108-2154C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694236 | ||||||
chr16:11694434
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-2352G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694434 | ||||||
chr16:11694575
|
G | A | 100 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(97): Show | 107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1108-2493C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694575 | ||||||
chr16:11694593
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 58 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1108-2511C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694593 | ||||||
chr16:11694732
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1108-2650G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694732 | ||||||
chr16:11694733
|
G | A | 1 | a0001c0008t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1108-2651C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694733 | ||||||
chr16:11694735
|
G | A | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1108-2653C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694735 | ||||||
chr16:11694832
|
A | T | 1 | a0003c0002t0001g0352 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1108-2750T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694832 | ||||||
chr16:11694854
|
C | CAACTT | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-2773_1108-277 others(9): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694854 | ||||||
chr16:11695038
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-2956A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695038 | ||||||
chr16:11695056
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 73 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1108-2974C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695056 | ||||||
chr16:11695234
|
T | C | 1 | a0003c0002t0001g0307 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1107+2891A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695234 | ||||||
chr16:11695334
|
C | T | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(152): Show | 168 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1107+2791G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695334 | ||||||
chr16:11695464
|
AGT | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+2659_1107+266 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695464 | ||||||
chr16:11695519
|
T | C | 26 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(23): Show | 29 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.1107+2606A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695519 | ||||||
chr16:11695616
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+2509G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695616 | ||||||
chr16:11695715
|
T | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1107+2410A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695715 | ||||||
chr16:11695733
|
G | T | 2 | a0001c0001t0001g0153a0004c0006t0001g0294 | 2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1107+2392C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695733 | ||||||
chr16:11695939
|
G | A | 1 | a0003c0002t0001g0297 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1107+2186C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695939 | ||||||
chr16:11696025
|
C | CA | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+2099dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696025 | ||||||
chr16:11696081
|
C | G | 1 | a0002c0003t0001g0152 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1107+2044G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696081 | ||||||
chr16:11696086
|
G | A | 1 | a0003c0002t0001g0337 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1107+2039C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696086 | ||||||
chr16:11696138
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1107+1987C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696138 | ||||||
chr16:11696224
|
G | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1107+1901C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696224 | ||||||
chr16:11696491
|
T | G | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1107+1634A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696491 | ||||||
chr16:11696614
|
C | A | 1 | a0001c0007t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1107+1511G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696614 | ||||||
chr16:11696693
|
A | G | 1 | a0002c0003t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1107+1432T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696693 | ||||||
chr16:11696805
|
C | T | 1 | a0003c0002t0001g0279 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1107+1320G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696805 | ||||||
chr16:11697201
|
A | T | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1107+924T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697201 | ||||||
chr16:11697229
|
A | C | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1107+896T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697229 | ||||||
chr16:11697241
|
C | G | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+884G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697241 | ||||||
chr16:11697262
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+863G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697262 | ||||||
chr16:11697316
|
C | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0046 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1107+809G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697316 | ||||||
chr16:11697431
|
G | C | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107+694C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697431 | ||||||
chr16:11697466
|
G | A | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1107+659C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697466 | ||||||
chr16:11697575
|
A | G | 1 | a0001c0004t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1107+550T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697575 | ||||||
chr16:11697680
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+445G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697680 | ||||||
chr16:11697855
|
G | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1107+270C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697855 | ||||||
chr16:11697974
|
T | C | 19 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(16): Show | 20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1107+151A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697974 | ||||||
chr16:11698016
|
G | C | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+109C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11698016 | ||||||
chr16:11698028
|
A | G | 2 | a0002c0005t0001g0027a0002c0005t0001g0032 | 2 | HG01261.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1107+97T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11698028 | ||||||
chr16:11698438
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0239 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.907-113C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698438 | ||||||
chr16:11698480
|
C | T | 1 | a0002c0003t0001g0260 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.907-155G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698480 | ||||||
chr16:11698595
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0111others(1): Show | 4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-270T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698595 | ||||||
chr16:11698598
|
C | T | 1 | a0003c0002t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.907-273G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698598 | ||||||
chr16:11698658
|
C | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(40): Show | 47 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.907-333G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698658 | ||||||
chr16:11698717
|
C | G | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.907-392G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698717 | ||||||
chr16:11698741
|
T | C | 1 | a0002c0003t0001g0168 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.907-416A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698741 | ||||||
chr16:11698798
|
T | C | 1 | a0002c0003t0001g0148 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.907-473A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698798 | ||||||
chr16:11698839
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.907-514G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698839 | ||||||
chr16:11698844
|
A | C | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.907-519T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698844 | ||||||
chr16:11698942
|
G | C | 1 | a0003c0002t0001g0349 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.907-617C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698942 | ||||||
chr16:11699053
|
A | C | 2 | a0002c0005t0001g0027a0002c0005t0001g0032 | 2 | HG01261.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.907-728T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699053 | ||||||
chr16:11699232
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.907-907A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699232 | ||||||
chr16:11699247
|
G | GT | 182 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(179): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.907-923_907-922ins others(1): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699247 | ||||||
chr16:11699374
|
T | C | 20 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(17): Show | 21 | HG01261.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.907-1049A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699374 | ||||||
chr16:11699440
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.906+1012C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699440 | ||||||
chr16:11699490
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+962C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699490 | ||||||
chr16:11699539
|
C | T | 168 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0012others(165): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.906+913G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699539 | ||||||
chr16:11699843
|
A | C | 20 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(17): Show | 21 | HG01261.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.906+609T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699843 | ||||||
chr16:11699962
|
A | T | 1 | a0002c0003t0001g0194 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.906+490T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699962 | ||||||
chr16:11699969
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.906+483G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699969 | ||||||
chr16:11700152
|
C | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0124others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+300G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700152 | ||||||
chr16:11700211
|
A | G | 63 | a0001c0001t0001g0008a0001c0004t0001g0040a0001c0004t0001g0045others(60): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.906+241T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700211 | ||||||
chr16:11700264
|
A | T | 1 | a0003c0002t0001g0350 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.906+188T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700264 | ||||||
chr16:11700289
|
T | C | 1 | a0002c0003t0001g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.906+163A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700289 | ||||||
chr16:11700337
|
A | G | 1 | a0002c0003t0002g0065 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.906+115T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700337 | ||||||
chr16:11700692
|
G | C | 4 | a0001c0001t0001g0153a0001c0004t0001g0043a0001c0004t0001g0046others(1): Show | 4 | HG03834.hp2 HG04228.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-128C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11700692 | ||||||
chr16:11700984
|
T | C | 3 | a0001c0001t0001g0271a0007c0013t0001g0112a0007c0013t0001g0113 | 3 | HG02145.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-420A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11700984 | ||||||
chr16:11701038
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-474G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701038 | ||||||
chr16:11701039
|
C | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(142): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.794-475G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701039 | ||||||
chr16:11701097
|
TTTA | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-536_794-534del others(3): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701097 | ||||||
chr16:11701128
|
C | CT | 32 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0093others(29): Show | 33 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-565dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | ||||||
chr16:11701128
|
CT | C | 20 | a0001c0001t0001g0091a0001c0001t0001g0116a0001c0001t0001g0184others(17): Show | 20 | HG00323.hp1 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.794-565delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | ||||||
chr16:11701128
|
CTTT | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(14): Show | 18 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-567_794-565del others(3): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | ||||||
chr16:11701128
|
CTTTTTTT others(4): Show |
C | 6 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(3): Show | 6 | HG02056.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-575_794-565del others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | ||||||
chr16:11701167
|
C | T | 1 | a0002c0003t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.794-603G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701167 | ||||||
chr16:11701168
|
G | A | 1 | a0003c0002t0001g0309 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.794-604C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701168 | ||||||
chr16:11701267
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.794-703C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701267 | ||||||
chr16:11701285
|
T | C | 4 | a0001c0004t0001g0025a0001c0004t0001g0026a0002c0011t0001g0062others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-721A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701285 | ||||||
chr16:11701357
|
G | A | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-793C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701357 | ||||||
chr16:11701417
|
G | C | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-853C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701417 | ||||||
chr16:11701723
|
C | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 86 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.794-1159G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701723 | ||||||
chr16:11701747
|
C | T | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-1183G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701747 | ||||||
chr16:11701806
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.794-1242C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701806 | ||||||
chr16:11701976
|
T | C | 1 | a0002c0003t0001g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794-1412A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701976 | ||||||
chr16:11702021
|
C | CA | 9 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-1458dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702021 | ||||||
chr16:11702034
|
A | G | 1 | a0003c0002t0001g0323 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.794-1470T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702034 | ||||||
chr16:11702056
|
ATGTGTGT others(7): Show |
A | 1 | a0003c0002t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.794-1506_794-1493d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702056 | ||||||
chr16:11702063
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.794-1499A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702063 | ||||||
chr16:11702066
|
A | G | 21 | a0002c0003t0001g0135a0002c0003t0001g0143a0002c0005t0001g0005others(18): Show | 23 | HG00280.hp1 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.794-1502T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702066 | ||||||
chr16:11702076
|
G | A | 15 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(12): Show | 16 | HG01106.hp2 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.794-1512C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702076 | ||||||
chr16:11702086
|
GTA | G | 13 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 14 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.794-1524_794-1523d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702086 | ||||||
chr16:11702088
|
A | G | 2 | a0002c0005t0001g0036a0003c0002t0001g0307 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.794-1524T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702088 | ||||||
chr16:11702090
|
G | A | 2 | a0002c0005t0001g0036a0003c0002t0001g0307 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.794-1526C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702090 | ||||||
chr16:11702091
|
T | C | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1527A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702091 | ||||||
chr16:11702092
|
G | A | 15 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(12): Show | 16 | HG01106.hp2 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.794-1528C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | ||||||
chr16:11702092
|
G | GTA | 17 | a0001c0001t0001g0110a0001c0001t0001g0256a0001c0025t0001g0100others(14): Show | 18 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-1530_794-1529d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | ||||||
chr16:11702092
|
G | GTATA | 3 | a0001c0014t0001g0068a0003c0002t0001g0016a0003c0002t0001g0352 | 4 | HG00280.hp1 HG01070.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1532_794-1529d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | ||||||
chr16:11702092
|
GTA | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(39): Show | 47 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.794-1530_794-1529d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | ||||||
chr16:11702094
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0237 | 2 | HG02145.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.794-1530T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702094 | ||||||
chr16:11702095
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-1531A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702095 | ||||||
chr16:11702096
|
A | G | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1532T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702096 | ||||||
chr16:11702097
|
T | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1533A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702097 | ||||||
chr16:11702110
|
A | G | 1 | a0002c0003t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.794-1546T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702110 | ||||||
chr16:11702187
|
T | C | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-1623A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702187 | ||||||
chr16:11702272
|
A | C | 1 | a0002c0003t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794-1708T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702272 | ||||||
chr16:11702295
|
G | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1731C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702295 | ||||||
chr16:11702335
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-1771G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702335 | ||||||
chr16:11702394
|
G | A | 1 | a0003c0002t0001g0016 | 2 | HG00280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-1830C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702394 | ||||||
chr16:11702405
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-1841A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702405 | ||||||
chr16:11702497
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.794-1933C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702497 | ||||||
chr16:11702523
|
C | T | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1959G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702523 | ||||||
chr16:11702620
|
A | C | 1 | a0006c0010t0001g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794-2056T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702620 | ||||||
chr16:11702688
|
A | G | 1 | a0003c0002t0001g0318 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.794-2124T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702688 | ||||||
chr16:11702695
|
T | A | 3 | a0001c0004t0001g0025a0001c0004t0001g0026a0001c0018t0001g0024 | 3 | HG02622.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.794-2131A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702695 | ||||||
chr16:11702703
|
T | A | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-2139A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702703 | ||||||
chr16:11702817
|
C | A | 7 | a0001c0014t0001g0068a0001c0018t0001g0024a0002c0003t0001g0129others(4): Show | 7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2253G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702817 | ||||||
chr16:11702901
|
A | G | 1 | a0003c0002t0001g0321 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.794-2337T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702901 | ||||||
chr16:11702932
|
A | T | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-2368T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702932 | ||||||
chr16:11702934
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(8): Show | 12 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-2370A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702934 | ||||||
chr16:11703012
|
G | A | 29 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(26): Show | 33 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-2448C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703012 | ||||||
chr16:11703016
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.794-2452G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703016 | ||||||
chr16:11703059
|
C | T | 1 | a0001c0025t0001g0100 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-2495G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703059 | ||||||
chr16:11703148
|
G | A | 4 | a0001c0004t0001g0006a0001c0004t0001g0044a0001c0004t0001g0055others(1): Show | 5 | NA18946.hp1 NA18973.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2584C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703148 | ||||||
chr16:11703509
|
T | TAC | 14 | a0001c0001t0001g0012a0001c0001t0001g0230a0001c0001t0001g0231others(11): Show | 15 | HG01243.hp1 HG01261.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.794-2947_794-2946d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
T | TACAC | 15 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0004t0001g0001others(12): Show | 18 | HG00408.hp1 HG02015.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2949_794-2946d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
T | TACACACA others(3): Show |
1 | a0001c0004t0001g0058 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.794-2955_794-2946d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
TAC | T | 91 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(88): Show | 94 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.794-2947_794-2946d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
TACAC | T | 86 | a0001c0001t0001g0153a0001c0007t0001g0004a0001c0007t0001g0022others(83): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.794-2949_794-2946d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
TACACAC | T | 4 | a0002c0003t0001g0161a0002c0011t0001g0062a0002c0011t0001g0063others(1): Show | 4 | HG03041.hp2 HG03540.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2951_794-2946d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
TACACACA others(7): Show |
T | 3 | a0001c0001t0001g0074a0001c0001t0001g0115a0002c0003t0001g0114 | 3 | HG02257.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.794-2959_794-2946d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703509
|
TACACACA others(9): Show |
T | 10 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2961_794-2946d others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | ||||||
chr16:11703513
|
C | CACACAT | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-2950_794-2949i others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703513 | ||||||
chr16:11703543
|
C | G | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-2979G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703543 | ||||||
chr16:11703664
|
G | C | 6 | a0001c0018t0001g0024a0002c0003t0001g0129a0002c0003t0001g0130others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-3100C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703664 | ||||||
chr16:11703723
|
G | A | 1 | a0002c0003t0001g0166 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.794-3159C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703723 | ||||||
chr16:11703863
|
G | A | 80 | a0001c0001t0001g0153a0002c0003t0001g0135a0002c0003t0001g0143others(77): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.794-3299C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703863 | ||||||
chr16:11704014
|
C | T | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-3450G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704014 | ||||||
chr16:11704421
|
A | G | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-3857T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704421 | ||||||
chr16:11704504
|
A | G | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-3940T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704504 | ||||||
chr16:11704579
|
C | A | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-4015G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704579 | ||||||
chr16:11704579
|
C | T | 7 | a0001c0014t0001g0068a0001c0018t0001g0024a0002c0003t0001g0129others(4): Show | 7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-4015G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704579 | ||||||
chr16:11704744
|
A | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-4180T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704744 | ||||||
chr16:11704829
|
A | G | 1 | a0003c0002t0001g0322 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-4265T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704829 | ||||||
chr16:11704862
|
G | C | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.794-4298C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704862 | ||||||
chr16:11704865
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(8): Show | 12 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-4301C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704865 | ||||||
chr16:11704888
|
C | G | 1 | a0012c0021t0001g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.794-4324G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704888 | ||||||
chr16:11704889
|
G | A | 2 | a0002c0003t0001g0192a0003c0002t0001g0284 | 2 | NA18948.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.794-4325C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704889 | ||||||
chr16:11704902
|
C | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.794-4338G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704902 | ||||||
chr16:11704915
|
C | CT | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-4352dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704915 | ||||||
chr16:11704932
|
C | T | 1 | a0001c0004t0001g0058 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.794-4368G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704932 | ||||||
chr16:11705020
|
G | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-4456C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705020 | ||||||
chr16:11705030
|
G | A | 1 | a0002c0003t0001g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.794-4466C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705030 | ||||||
chr16:11705035
|
T | C | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-4471A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705035 | ||||||
chr16:11705051
|
T | C | 5 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(2): Show | 5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-4487A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705051 | ||||||
chr16:11705497
|
A | AAG | 5 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0036others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-4935_794-4934d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705497 | ||||||
chr16:11705511
|
C | A | 81 | a0001c0001t0001g0153a0002c0003t0001g0135a0002c0003t0001g0143others(78): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.794-4947G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705511 | ||||||
chr16:11705598
|
C | G | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-5034G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705598 | ||||||
chr16:11705709
|
C | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-5145G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705709 | ||||||
chr16:11705728
|
C | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(32): Show | 37 | HG00609.hp2 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.794-5164G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705728 | ||||||
chr16:11705775
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-5211C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705775 | ||||||
chr16:11705817
|
G | A | 1 | a0003c0002t0001g0305 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-5253C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705817 | ||||||
chr16:11705848
|
A | C | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-5284T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705848 | ||||||
chr16:11705884
|
G | A | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-5320C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705884 | ||||||
chr16:11706160
|
G | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG03471.hp2 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-5596C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706160 | ||||||
chr16:11706165
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-5601G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706165 | ||||||
chr16:11706363
|
C | A | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-5799G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706363 | ||||||
chr16:11706548
|
A | C | 1 | a0002c0003t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.794-5984T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706548 | ||||||
chr16:11706758
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-6194G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706758 | ||||||
chr16:11706912
|
A | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-6348T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706912 | ||||||
chr16:11706940
|
T | C | 1 | a0003c0002t0001g0307 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6376A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706940 | ||||||
chr16:11706992
|
C | T | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.794-6428G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706992 | ||||||
chr16:11706996
|
G | C | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-6432C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706996 | ||||||
chr16:11707049
|
T | G | 1 | a0003c0002t0001g0307 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6485A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707049 | ||||||
chr16:11707060
|
C | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-6496G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707060 | ||||||
chr16:11707139
|
G | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-6575C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707139 | ||||||
chr16:11707234
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0244 | 2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.794-6670G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707234 | ||||||
chr16:11707317
|
G | A | 1 | a0003c0002t0001g0307 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6753C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707317 | ||||||
chr16:11707454
|
A | AT | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.794-6891dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707454 | ||||||
chr16:11707814
|
G | A | 2 | a0002c0005t0001g0028a0002c0005t0001g0031 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.794-7250C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707814 | ||||||
chr16:11707817
|
C | A | 30 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(27): Show | 34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.794-7253G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707817 | ||||||
chr16:11707953
|
G | A | 5 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(2): Show | 5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-7389C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707953 | ||||||
chr16:11708023
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0124a0001c0001t0001g0126 | 4 | HG01167.hp2 HG01169.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-7459C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708023 | ||||||
chr16:11708026
|
G | T | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-7462C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708026 | ||||||
chr16:11708110
|
T | G | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-7546A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708110 | ||||||
chr16:11708239
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-7675A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708239 | ||||||
chr16:11708396
|
G | A | 1 | a0001c0017t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-7832C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708396 | ||||||
chr16:11708397
|
C | A | 1 | a0001c0017t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-7833G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708397 | ||||||
chr16:11708597
|
T | C | 1 | a0003c0002t0001g0321 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.794-8033A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708597 | ||||||
chr16:11708870
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-8306T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708870 | ||||||
chr16:11708971
|
T | A | 15 | a0002c0003t0001g0181a0002c0005t0001g0005a0002c0005t0001g0027others(12): Show | 16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-8407A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708971 | ||||||
chr16:11709130
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-8566A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709130 | ||||||
chr16:11709259
|
C | CTTTTTTT others(2): Show |
127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.794-8704_794-8696d others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709259 | ||||||
chr16:11709259
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0094a0001c0001t0001g0242a0001c0001t0001g0252others(2): Show | 5 | HG01358.hp1 HG02622.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-8705_794-8696d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709259 | ||||||
chr16:11709377
|
C | T | 40 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(37): Show | 42 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.794-8813G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709377 | ||||||
chr16:11709414
|
ATTTTTTG others(10): Show |
A | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-8867_794-8851d others(19): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709414 | ||||||
chr16:11709423
|
A | AT | 29 | a0001c0001t0001g0115a0001c0001t0001g0271a0002c0003t0001g0114others(26): Show | 30 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.794-8860dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
A | ATTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-8862_794-8860d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
A | T | 1 | a0002c0003t0001g0135 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.794-8859T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
AT | A | 18 | a0001c0001t0001g0120a0001c0001t0001g0205a0001c0001t0001g0225others(15): Show | 18 | HG00544.hp2 HG00673.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-8860delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
ATT | A | 89 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(86): Show | 94 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.794-8861_794-8860d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
ATTT | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 51 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.794-8862_794-8860d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
ATTTTTTT others(3): Show |
A | 25 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(22): Show | 28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.794-8869_794-8860d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0017t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-8870_794-8860d others(13): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709423
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-8871_794-8860d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | ||||||
chr16:11709495
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-8931G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709495 | ||||||
chr16:11709554
|
C | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-8990G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709554 | ||||||
chr16:11709591
|
T | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-9027A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709591 | ||||||
chr16:11709637
|
A | G | 1 | a0001c0025t0001g0100 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-9073T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709637 | ||||||
chr16:11709682
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0104others(1): Show | 5 | HG00609.hp2 HG00621.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-9118C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709682 | ||||||
chr16:11709683
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0108others(1): Show | 4 | NA18939.hp1 NA18980.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-9119G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709683 | ||||||
chr16:11709785
|
G | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.794-9221C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709785 | ||||||
chr16:11710042
|
C | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.794-9478G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710042 | ||||||
chr16:11710101
|
C | T | 1 | a0002c0003t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.794-9537G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710101 | ||||||
chr16:11710126
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.794-9562C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710126 | ||||||
chr16:11710198
|
AT | A | 234 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(231): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.794-9635delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710198 | ||||||
chr16:11710336
|
C | CAT | 196 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.794-9773_794-9772i others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710336 | ||||||
chr16:11710336
|
C | T | 1 | a0002c0003t0001g0150 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.794-9772G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710336 | ||||||
chr16:11710529
|
C | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.794-9965G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710529 | ||||||
chr16:11710592
|
G | A | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-10028C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710592 | ||||||
chr16:11710709
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.794-10145G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710709 | ||||||
chr16:11710781
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0244 | 2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.794-10217G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710781 | ||||||
chr16:11710806
|
C | T | 1 | a0002c0003t0001g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794-10242G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710806 | ||||||
chr16:11710873
|
A | G | 15 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(12): Show | 16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-10309T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710873 | ||||||
chr16:11710944
|
G | A | 1 | a0002c0003t0001g0183 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.794-10380C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710944 | ||||||
chr16:11710974
|
A | ACAG | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-10413_794-1041 others(7): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710974 | ||||||
chr16:11710992
|
A | C | 1 | a0003c0002t0001g0344 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.794-10428T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710992 | ||||||
chr16:11711001
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.794-10437A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711001 | ||||||
chr16:11711169
|
C | CAT | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+10406_793+1040 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711169 | ||||||
chr16:11711176
|
T | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+10401A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711176 | ||||||
chr16:11711186
|
T | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+10391A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711186 | ||||||
chr16:11711716
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0070others(13): Show | 17 | NA18942.hp1 NA18943.hp2 NA18960.hp2 others(14): Show |
intron_variant | MODIFIER | c.793+9861A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711716 | ||||||
chr16:11711767
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.793+9810T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711767 | ||||||
chr16:11711970
|
G | C | 1 | a0007c0013t0001g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.793+9607C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711970 | ||||||
chr16:11711998
|
A | C | 1 | a0003c0002t0001g0334 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.793+9579T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711998 | ||||||
chr16:11712010
|
T | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+9567A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712010 | ||||||
chr16:11712022
|
T | C | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.793+9555A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712022 | ||||||
chr16:11712098
|
C | T | 1 | a0017c0028t0001g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.793+9479G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712098 | ||||||
chr16:11712143
|
G | C | 1 | a0002c0003t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.793+9434C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712143 | ||||||
chr16:11712156
|
A | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 75 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.793+9421T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712156 | ||||||
chr16:11712214
|
G | A | 15 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(12): Show | 16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+9363C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712214 | ||||||
chr16:11712215
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793+9362C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712215 | ||||||
chr16:11712649
|
T | C | 1 | a0002c0003t0001g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793+8928A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712649 | ||||||
chr16:11712858
|
T | G | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8719A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712858 | ||||||
chr16:11712922
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8655G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712922 | ||||||
chr16:11712929
|
A | AAACACAC others(6): Show |
1 | a0014c0027t0001g0270 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.793+8647_793+8648i others(15): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AAC | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.793+8646_793+8647d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACAC | 10 | a0001c0001t0001g0072a0001c0001t0001g0106a0001c0004t0001g0026others(7): Show | 10 | HG00741.hp2 HG02027.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+8644_793+8647d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACAC | 21 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(18): Show | 22 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+8642_793+8647d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(1): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0206a0002c0005t0001g0033 | 3 | HG02896.hp2 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.793+8640_793+8647d others(10): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(3): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01346.hp2 HG03471.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+8638_793+8647d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(5): Show |
43 | a0001c0001t0001g0014a0001c0001t0001g0116a0001c0001t0001g0202others(40): Show | 44 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.793+8636_793+8647d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(7): Show |
12 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0211others(9): Show | 14 | HG01175.hp2 HG01496.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.793+8634_793+8647d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(9): Show |
6 | a0001c0001t0001g0012a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 7 | HG02165.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+8632_793+8647d others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
A | AACACACA others(11): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG01070.hp2 HG01071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.793+8630_793+8647d others(20): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
AACACAC | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0251others(1): Show | 4 | HG01256.hp1 HG01358.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+8642_793+8647d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712929
|
AACACACA others(5): Show |
A | 6 | a0002c0003t0001g0164a0002c0003t0001g0166a0002c0003t0001g0168others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+8636_793+8647d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | ||||||
chr16:11712959
|
G | C | 1 | a0002c0003t0002g0064 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.793+8618C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712959 | ||||||
chr16:11713048
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0246 | 2 | NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.793+8529C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713048 | ||||||
chr16:11713052
|
A | G | 1 | a0003c0002t0001g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.793+8525T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713052 | ||||||
chr16:11713095
|
G | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8482C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713095 | ||||||
chr16:11713110
|
G | GA | 91 | a0001c0001t0001g0153a0001c0004t0001g0047a0002c0003t0001g0135others(88): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.793+8466dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713110
|
G | GAA | 9 | a0003c0002t0001g0300a0003c0002t0001g0301a0003c0002t0001g0305others(6): Show | 9 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+8465_793+8466d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713110
|
GA | G | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 83 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.793+8466delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713110
|
GAA | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0070a0001c0001t0001g0115others(17): Show | 21 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+8465_793+8466d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713110
|
GAAA | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(37): Show | 42 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.793+8464_793+8466d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713110
|
GAAAA | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+8463_793+8466d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | ||||||
chr16:11713111
|
A | G | 1 | a0001c0004t0001g0049 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.793+8466T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713111 | ||||||
chr16:11713241
|
T | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+8336A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713241 | ||||||
chr16:11713280
|
C | CA | 37 | a0001c0001t0001g0010a0001c0001t0001g0123a0001c0001t0001g0124others(34): Show | 41 | HG00408.hp1 HG00544.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.793+8296dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713280 | ||||||
chr16:11713280
|
CA | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 56 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.793+8296delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713280 | ||||||
chr16:11713511
|
G | C | 1 | a0002c0011t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.793+8066C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713511 | ||||||
chr16:11713582
|
A | C | 1 | a0001c0004t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.793+7995T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713582 | ||||||
chr16:11713606
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | NA18952.hp2 NA19004.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.793+7971C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713606 | ||||||
chr16:11713657
|
C | A | 4 | a0002c0003t0002g0064a0002c0003t0002g0065a0002c0003t0002g0066others(1): Show | 4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+7920G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713657 | ||||||
chr16:11713661
|
G | C | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.793+7916C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713661 | ||||||
chr16:11713773
|
G | A | 1 | a0002c0011t0001g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793+7804C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713773 | ||||||
chr16:11713886
|
G | A | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+7691C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713886 | ||||||
chr16:11713983
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0244 | 2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.793+7594A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713983 | ||||||
chr16:11713990
|
T | C | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+7587A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713990 | ||||||
chr16:11714024
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+7553C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714024 | ||||||
chr16:11714046
|
A | AT | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.793+7530dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714046 | ||||||
chr16:11714067
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.793+7510C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714067 | ||||||
chr16:11714257
|
C | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+7320G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714257 | ||||||
chr16:11714287
|
G | C | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.793+7290C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714287 | ||||||
chr16:11714289
|
G | T | 1 | a0002c0003t0001g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.793+7288C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714289 | ||||||
chr16:11714358
|
T | G | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+7219A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714358 | ||||||
chr16:11714496
|
C | T | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+7081G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714496 | ||||||
chr16:11714588
|
C | T | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+6989G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714588 | ||||||
chr16:11714611
|
G | A | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.793+6966C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714611 | ||||||
chr16:11714639
|
C | CA | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+6937dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714639 | ||||||
chr16:11714726
|
A | T | 4 | a0001c0004t0001g0025a0001c0004t0001g0026a0002c0011t0001g0062others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+6851T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714726 | ||||||
chr16:11714871
|
G | A | 4 | a0001c0004t0001g0025a0001c0004t0001g0026a0002c0011t0001g0062others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+6706C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714871 | ||||||
chr16:11714913
|
A | C | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+6664T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714913 | ||||||
chr16:11714950
|
T | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+6627A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714950 | ||||||
chr16:11715127
|
C | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0111others(1): Show | 4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+6450G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715127 | ||||||
chr16:11715184
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0111others(1): Show | 4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+6393C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715184 | ||||||
chr16:11715200
|
A | C | 1 | a0001c0007t0001g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.793+6377T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715200 | ||||||
chr16:11715424
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.793+6153G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715424 | ||||||
chr16:11715462
|
CA | C | 196 | a0001c0001t0001g0153a0001c0001t0001g0240a0001c0001t0001g0264others(193): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.793+6114delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | ||||||
chr16:11715462
|
CAA | C | 131 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(128): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.793+6113_793+6114d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | ||||||
chr16:11715462
|
CAAA | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+6112_793+6114d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | ||||||
chr16:11715562
|
A | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+6015T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715562 | ||||||
chr16:11715836
|
C | T | 4 | a0003c0002t0001g0285a0003c0002t0001g0334a0003c0002t0001g0335others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+5741G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715836 | ||||||
chr16:11715865
|
T | G | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+5712A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715865 | ||||||
chr16:11715945
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.793+5632T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715945 | ||||||
chr16:11715980
|
G | A | 1 | a0002c0003t0001g0182 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.793+5597C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715980 | ||||||
chr16:11716083
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.793+5494G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716083 | ||||||
chr16:11716084
|
A | G | 191 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(188): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.793+5493T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716084 | ||||||
chr16:11716526
|
T | C | 196 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.793+5051A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716526 | ||||||
chr16:11716534
|
T | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+5043A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716534 | ||||||
chr16:11716618
|
A | G | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+4959T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716618 | ||||||
chr16:11717002
|
G | T | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793+4575C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717002 | ||||||
chr16:11717108
|
G | GA | 14 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0243others(11): Show | 14 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.793+4468dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717108 | ||||||
chr16:11717109
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.793+4468T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717109 | ||||||
chr16:11717140
|
A | C | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+4437T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717140 | ||||||
chr16:11717190
|
C | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+4387G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717190 | ||||||
chr16:11717311
|
G | A | 77 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.793+4266C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717311 | ||||||
chr16:11717366
|
C | T | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+4211G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717366 | ||||||
chr16:11717434
|
G | GA | 101 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(98): Show | 106 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.793+4142dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | ||||||
chr16:11717434
|
G | GAA | 11 | a0001c0001t0001g0115a0001c0001t0001g0205a0001c0001t0001g0206others(8): Show | 11 | HG01192.hp2 HG02257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+4141_793+4142d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | ||||||
chr16:11717434
|
GA | G | 35 | a0001c0001t0001g0102a0001c0004t0001g0001a0001c0004t0001g0006others(32): Show | 38 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.793+4142delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | ||||||
chr16:11717436
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.793+4141T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717436 | ||||||
chr16:11717547
|
C | T | 2 | a0004c0006t0001g0003a0004c0006t0001g0351 | 4 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+4030G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717547 | ||||||
chr16:11717587
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214others(2): Show | 5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+3990G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717587 | ||||||
chr16:11717639
|
G | T | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3938C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717639 | ||||||
chr16:11717640
|
TGAAACCC others(353): Show |
T | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3577_793+3936d others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717640 | ||||||
chr16:11717872
|
G | C | 32 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0025others(29): Show | 36 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.793+3705C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717872 | ||||||
chr16:11717933
|
C | T | 77 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.793+3644G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717933 | ||||||
chr16:11718003
|
G | A | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3574C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718003 | ||||||
chr16:11718004
|
T | C | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3573A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718004 | ||||||
chr16:11718019
|
T | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3558A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718019 | ||||||
chr16:11718021
|
T | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3556A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718021 | ||||||
chr16:11718027
|
T | A | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3550A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718027 | ||||||
chr16:11718031
|
T | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3546A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718031 | ||||||
chr16:11718032
|
A | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3545T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718032 | ||||||
chr16:11718033
|
A | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3544T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718033 | ||||||
chr16:11718034
|
A | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3543T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718034 | ||||||
chr16:11718035
|
A | G | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3542T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718035 | ||||||
chr16:11718036
|
A | T | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3541T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718036 | ||||||
chr16:11718059
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+3518C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718059 | ||||||
chr16:11718164
|
A | C | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3413T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718164 | ||||||
chr16:11718165
|
T | A | 2 | a0002c0003t0001g0134a0002c0003t0001g0183 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3412A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718165 | ||||||
chr16:11718216
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0110 | 2 | HG00733.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.793+3361C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718216 | ||||||
chr16:11718219
|
T | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+3358A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718219 | ||||||
chr16:11718271
|
T | TA | 30 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(27): Show | 34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.793+3305dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718271 | ||||||
chr16:11718381
|
T | C | 1 | a0002c0003t0001g0172 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+3196A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718381 | ||||||
chr16:11718435
|
C | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(162): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.793+3142G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718435 | ||||||
chr16:11718489
|
C | CT | 8 | a0001c0001t0001g0202a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | NA18612.hp2 NA18955.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+3087dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718489 | ||||||
chr16:11718602
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+2975T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718602 | ||||||
chr16:11718693
|
A | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+2884T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718693 | ||||||
chr16:11719089
|
T | C | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+2488A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719089 | ||||||
chr16:11719358
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0244a0005c0009t0001g0253 | 3 | HG01496.hp1 HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.793+2219G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719358 | ||||||
chr16:11719489
|
T | C | 1 | a0003c0002t0001g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793+2088A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719489 | ||||||
chr16:11719789
|
C | T | 1 | a0005c0009t0001g0253 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793+1788G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719789 | ||||||
chr16:11719880
|
C | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+1697G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719880 | ||||||
chr16:11720043
|
G | A | 148 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(145): Show | 156 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.793+1534C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720043 | ||||||
chr16:11720240
|
A | G | 21 | a0002c0003t0001g0142a0002c0003t0001g0157a0002c0003t0001g0158others(18): Show | 21 | HG00408.hp2 HG00621.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.793+1337T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720240 | ||||||
chr16:11720416
|
A | AT | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.793+1160dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720416 | ||||||
chr16:11720416
|
AT | A | 25 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(22): Show | 28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.793+1160delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720416 | ||||||
chr16:11720515
|
A | G | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+1062T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720515 | ||||||
chr16:11720664
|
G | A | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793+913C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720664 | ||||||
chr16:11720706
|
C | T | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.793+871G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720706 | ||||||
chr16:11720748
|
T | G | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+829A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720748 | ||||||
chr16:11721074
|
C | T | 1 | a0002c0005t0001g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.793+503G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721074 | ||||||
chr16:11721165
|
C | T | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+412G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721165 | ||||||
chr16:11721322
|
C | T | 193 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 206 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.793+255G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721322 | ||||||
chr16:11721362
|
A | G | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+215T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721362 | ||||||
chr16:11721418
|
G | A | 2 | a0001c0001t0001g0115a0002c0003t0001g0114 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.793+159C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721418 | ||||||
chr16:11721438
|
A | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+139T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721438 | ||||||
chr16:11721464
|
C | G | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+113G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721464 | ||||||
chr16:11721470
|
G | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+107C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721470 | ||||||
chr16:11721476
|
G | A | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+101C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721476 | ||||||
chr16:11721516
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.793+61C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721516 | ||||||
chr16:11721525
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.793+52A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721525 | ||||||
chr16:11721953
|
G | A | 1 | a0002c0003t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.700-283C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11721953 | ||||||
chr16:11722035
|
G | A | 1 | a0001c0004t0001g0057 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700-365C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722035 | ||||||
chr16:11722048
|
C | A | 1 | a0002c0005t0001g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-378G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722048 | ||||||
chr16:11722108
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-438G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722108 | ||||||
chr16:11722209
|
C | G | 1 | a0003c0002t0001g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.700-539G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722209 | ||||||
chr16:11722251
|
C | G | 1 | a0002c0003t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700-581G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722251 | ||||||
chr16:11722399
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.700-729A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722399 | ||||||
chr16:11722757
|
T | C | 2 | a0006c0010t0001g0272a0006c0010t0001g0273 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700-1087A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722757 | ||||||
chr16:11722815
|
G | A | 192 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.700-1145C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722815 | ||||||
chr16:11722996
|
C | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-1326G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722996 | ||||||
chr16:11722999
|
G | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-1329C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722999 | ||||||
chr16:11723121
|
G | A | 4 | a0001c0004t0001g0025a0001c0004t0001g0026a0002c0011t0001g0062others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-1451C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723121 | ||||||
chr16:11723149
|
T | A | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.700-1479A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723149 | ||||||
chr16:11723193
|
G | A | 28 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(25): Show | 32 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.700-1523C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723193 | ||||||
chr16:11723251
|
G | A | 192 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.700-1581C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723251 | ||||||
chr16:11723278
|
GAAAA | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(13): Show | 17 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.700-1612_700-1609d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723278 | ||||||
chr16:11723351
|
G | T | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.700-1681C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723351 | ||||||
chr16:11723356
|
A | G | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.700-1686T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723356 | ||||||
chr16:11723372
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.700-1702C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723372 | ||||||
chr16:11723391
|
C | T | 1 | a0011c0020t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.700-1721G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723391 | ||||||
chr16:11723517
|
G | A | 2 | a0007c0013t0001g0112a0007c0013t0001g0113 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.700-1847C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723517 | ||||||
chr16:11723610
|
A | C | 16 | a0002c0003t0001g0139a0002c0003t0001g0197a0002c0005t0001g0005others(13): Show | 17 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.700-1940T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723610 | ||||||
chr16:11724093
|
G | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.700-2423C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724093 | ||||||
chr16:11724642
|
T | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-2972A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724642 | ||||||
chr16:11724698
|
T | C | 6 | a0002c0003t0002g0064a0002c0003t0002g0065a0002c0003t0002g0066others(3): Show | 6 | NA18951.hp2 NA19010.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.700-3028A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724698 | ||||||
chr16:11724730
|
C | G | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.700-3060G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724730 | ||||||
chr16:11724851
|
T | C | 22 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(19): Show | 25 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.700-3181A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724851 | ||||||
chr16:11724961
|
G | C | 1 | a0001c0018t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.700-3291C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724961 | ||||||
chr16:11724982
|
T | C | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.700-3312A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724982 | ||||||
chr16:11725034
|
G | A | 1 | a0002c0003t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.700-3364C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725034 | ||||||
chr16:11725112
|
G | A | 1 | a0003c0002t0001g0016 | 2 | HG00280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.700-3442C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725112 | ||||||
chr16:11725344
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.700-3674A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725344 | ||||||
chr16:11725356
|
T | C | 1 | a0002c0003t0001g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.700-3686A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725356 | ||||||
chr16:11725358
|
GA | G | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-3689delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725358 | ||||||
chr16:11725392
|
C | A | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.700-3722G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725392 | ||||||
chr16:11725406
|
A | T | 1 | a0002c0003t0001g0192 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.700-3736T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725406 | ||||||
chr16:11725474
|
G | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-3804C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725474 | ||||||
chr16:11725538
|
C | T | 1 | a0002c0003t0001g0141 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.700-3868G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725538 | ||||||
chr16:11725567
|
T | C | 1 | a0003c0002t0001g0332 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.700-3897A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725567 | ||||||
chr16:11725570
|
C | T | 4 | a0002c0011t0001g0062a0002c0011t0001g0063a0006c0010t0001g0272others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-3900G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725570 | ||||||
chr16:11725713
|
C | A | 188 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(185): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.700-4043G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725713 | ||||||
chr16:11725796
|
C | T | 1 | a0014c0027t0001g0270 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-4126G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725796 | ||||||
chr16:11725904
|
C | G | 1 | a0002c0003t0002g0064 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.700-4234G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725904 | ||||||
chr16:11726123
|
T | G | 1 | a0001c0004t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.700-4453A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726123 | ||||||
chr16:11726147
|
G | C | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-4477C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726147 | ||||||
chr16:11726222
|
AGC | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.699+4421_699+4422d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726222 | ||||||
chr16:11726293
|
C | T | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.699+4352G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726293 | ||||||
chr16:11726311
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+4334C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726311 | ||||||
chr16:11726364
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.699+4281G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726364 | ||||||
chr16:11726389
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.699+4256A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726389 | ||||||
chr16:11726400
|
G | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.699+4245C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726400 | ||||||
chr16:11726550
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0084 | 2 | NA18967.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.699+4095T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726550 | ||||||
chr16:11726567
|
G | A | 1 | a0003c0002t0001g0338 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.699+4078C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726567 | ||||||
chr16:11726579
|
C | CA | 30 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0026others(27): Show | 34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.699+4065dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726579 | ||||||
chr16:11726579
|
CA | C | 142 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 150 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.699+4065delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726579 | ||||||
chr16:11726856
|
A | T | 1 | a0002c0003t0001g0192 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.699+3789T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726856 | ||||||
chr16:11727009
|
C | T | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+3636G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727009 | ||||||
chr16:11727032
|
G | A | 4 | a0003c0002t0001g0285a0003c0002t0001g0334a0003c0002t0001g0335others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+3613C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727032 | ||||||
chr16:11727040
|
G | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.699+3605C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727040 | ||||||
chr16:11727072
|
T | C | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.699+3573A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727072 | ||||||
chr16:11727113
|
T | A | 1 | a0003c0002t0001g0289 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.699+3532A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727113 | ||||||
chr16:11727115
|
A | T | 1 | a0003c0002t0001g0289 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.699+3530T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727115 | ||||||
chr16:11727195
|
AT | A | 25 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(22): Show | 28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.699+3449delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727195 | ||||||
chr16:11727204
|
C | T | 1 | a0003c0002t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.699+3441G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727204 | ||||||
chr16:11727598
|
G | A | 72 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 76 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.699+3047C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727598 | ||||||
chr16:11727643
|
C | T | 1 | a0003c0002t0001g0313 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.699+3002G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727643 | ||||||
chr16:11727652
|
A | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 84 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.699+2993T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727652 | ||||||
chr16:11727662
|
G | GC | 40 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0081others(37): Show | 41 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.699+2982dupG | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727662 | ||||||
chr16:11727670
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0108others(1): Show | 4 | NA18939.hp1 NA18980.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+2975G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727670 | ||||||
chr16:11727788
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 56 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.699+2857C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727788 | ||||||
chr16:11727852
|
G | A | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.699+2793C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727852 | ||||||
chr16:11728111
|
T | A | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.699+2534A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728111 | ||||||
chr16:11728143
|
A | T | 2 | a0002c0003t0001g0139a0002c0003t0001g0197 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.699+2502T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728143 | ||||||
chr16:11728210
|
T | C | 82 | a0002c0003t0001g0135a0002c0003t0001g0172a0002c0003t0001g0204others(79): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.699+2435A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728210 | ||||||
chr16:11728292
|
A | G | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.699+2353T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728292 | ||||||
chr16:11728538
|
A | C | 1 | a0002c0003t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.699+2107T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728538 | ||||||
chr16:11728592
|
C | A | 1 | a0002c0003t0001g0183 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.699+2053G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728592 | ||||||
chr16:11728802
|
C | G | 2 | a0003c0002t0001g0311a0003c0002t0001g0312 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.699+1843G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728802 | ||||||
chr16:11729000
|
A | AAATC | 15 | a0002c0003t0001g0200a0002c0005t0001g0005a0002c0005t0001g0027others(12): Show | 16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.699+1641_699+1644d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729000 | ||||||
chr16:11729464
|
T | TAG | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.699+1179_699+1180d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729464 | ||||||
chr16:11729514
|
T | C | 3 | a0006c0010t0001g0272a0006c0010t0001g0273a0006c0010t0001g0274 | 3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.699+1131A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729514 | ||||||
chr16:11729819
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.699+826C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729819 | ||||||
chr16:11729965
|
C | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.699+680G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729965 | ||||||
chr16:11730063
|
G | A | 6 | a0001c0004t0001g0040a0001c0004t0001g0045a0001c0004t0001g0058others(3): Show | 6 | HG00408.hp1 HG02015.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.699+582C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730063 | ||||||
chr16:11730139
|
G | A | 1 | a0002c0003t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.699+506C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730139 | ||||||
chr16:11730196
|
C | G | 6 | a0001c0014t0001g0068a0002c0003t0001g0129a0002c0003t0001g0130others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.699+449G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730196 | ||||||
chr16:11730200
|
T | G | 134 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 141 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.699+445A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730200 | ||||||
chr16:11730476
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.699+169A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730476 | ||||||
chr16:11730535
|
T | C | 1 | a0002c0003t0001g0194 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.699+110A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730535 | ||||||
chr16:11730783
|
AAAAAAT | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110 | 3 | HG00733.hp1 HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.570-15_570-10delAT others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730783 | ||||||
chr16:11730842
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.570-68A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730842 | ||||||
chr16:11730904
|
C | A | 7 | a0002c0005t0001g0005a0002c0005t0001g0033a0002c0005t0001g0034others(4): Show | 8 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.570-130G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730904 | ||||||
chr16:11731047
|
C | G | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.570-273G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731047 | ||||||
chr16:11731256
|
A | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 59 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.570-482T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731256 | ||||||
chr16:11731657
|
T | G | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.570-883A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731657 | ||||||
chr16:11731687
|
T | TCA | 22 | a0001c0001t0001g0076a0001c0001t0001g0258a0001c0001t0001g0259others(19): Show | 23 | HG00621.hp2 HG01106.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.570-915_570-914dup others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | ||||||
chr16:11731687
|
T | TCACA | 3 | a0002c0005t0001g0037a0002c0011t0001g0062a0002c0011t0001g0063 | 3 | HG01891.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.570-917_570-914dup others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | ||||||
chr16:11731687
|
TCA | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(48): Show | 53 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.570-915_570-914del others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | ||||||
chr16:11731687
|
TCACACAC others(9): Show |
T | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.570-929_570-914del others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | ||||||
chr16:11731716
|
C | T | 1 | a0002c0003t0001g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.570-942G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731716 | ||||||
chr16:11732012
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.570-1238C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732012 | ||||||
chr16:11732120
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121 | 3 | HG03654.hp2 HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570-1346G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732120 | ||||||
chr16:11732157
|
C | T | 192 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.570-1383G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732157 | ||||||
chr16:11732292
|
T | C | 79 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 83 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.570-1518A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732292 | ||||||
chr16:11732308
|
C | T | 1 | a0001c0014t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570-1534G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732308 | ||||||
chr16:11732309
|
G | A | 1 | a0002c0003t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570-1535C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732309 | ||||||
chr16:11732399
|
C | A | 6 | a0002c0003t0001g0142a0002c0003t0001g0170a0002c0003t0001g0171others(3): Show | 6 | NA18941.hp1 NA18952.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+1583G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732399 | ||||||
chr16:11732424
|
G | A | 1 | a0003c0002t0001g0343 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.569+1558C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732424 | ||||||
chr16:11732729
|
G | A | 1 | a0002c0023t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.569+1253C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732729 | ||||||
chr16:11732818
|
G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.569+1164C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732818 | ||||||
chr16:11732824
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.569+1158C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732824 | ||||||
chr16:11732985
|
T | C | 195 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.569+997A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732985 | ||||||
chr16:11733034
|
G | A | 5 | a0002c0003t0001g0138a0002c0003t0001g0185a0002c0003t0001g0186others(2): Show | 5 | HG01109.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+948C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733034 | ||||||
chr16:11733149
|
C | T | 1 | a0001c0007t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.569+833G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733149 | ||||||
chr16:11733188
|
G | A | 1 | a0002c0003t0001g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.569+794C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733188 | ||||||
chr16:11733204
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.569+778G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733204 | ||||||
chr16:11733296
|
T | A | 1 | a0003c0002t0001g0352 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.569+686A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733296 | ||||||
chr16:11733449
|
T | C | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.569+533A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733449 | ||||||
chr16:11733564
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.569+418A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733564 | ||||||
chr16:11733674
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.569+308G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733674 | ||||||
chr16:11733687
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.569+295C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733687 | ||||||
chr16:11733690
|
T | C | 55 | a0002c0003t0001g0172a0002c0003t0001g0204a0003c0002t0001g0002others(52): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.569+292A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733690 | ||||||
chr16:11734109
|
C | T | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.472-30G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734109 | ||||||
chr16:11734116
|
T | C | 2 | a0001c0001t0001g0115a0002c0003t0001g0114 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.472-37A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734116 | ||||||
chr16:11734162
|
A | G | 300 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(297): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.472-83T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734162 | ||||||
chr16:11734209
|
T | C | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-130A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734209 | ||||||
chr16:11734287
|
T | G | 1 | a0002c0003t0001g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.472-208A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734287 | ||||||
chr16:11734425
|
T | A | 81 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 85 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.472-346A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734425 | ||||||
chr16:11734426
|
T | A | 192 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.472-347A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734426 | ||||||
chr16:11734550
|
C | A | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.472-471G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734550 | ||||||
chr16:11734711
|
G | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0069others(39): Show | 44 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.472-632C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734711 | ||||||
chr16:11734845
|
A | T | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.472-766T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734845 | ||||||
chr16:11734882
|
A | G | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-803T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734882 | ||||||
chr16:11735159
|
T | G | 1 | a0001c0001t0001g0261 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.471+858A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735159 | ||||||
chr16:11735317
|
C | T | 3 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+700G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735317 | ||||||
chr16:11735353
|
T | C | 4 | a0003c0002t0001g0344a0004c0006t0001g0003a0004c0006t0001g0351others(1): Show | 6 | HG02056.hp2 NA18940.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+664A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735353 | ||||||
chr16:11735385
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.471+632C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735385 | ||||||
chr16:11735514
|
CT | C | 5 | a0002c0003t0001g0129a0002c0003t0001g0130a0002c0003t0001g0131others(2): Show | 5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+502delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735514 | ||||||
chr16:11735517
|
G | C | 1 | a0006c0010t0001g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+500C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735517 | ||||||
chr16:11735543
|
G | T | 1 | a0003c0002t0001g0288 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.471+474C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735543 | ||||||
chr16:11735863
|
C | A | 1 | a0009c0019t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.471+154G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735863 | ||||||
chr16:11736348
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255-115A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11736348 | ||||||
chr16:11736919
|
G | A | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-686C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11736919 | ||||||
chr16:11737082
|
T | C | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-849A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737082 | ||||||
chr16:11737174
|
T | C | 197 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 210 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.255-941A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737174 | ||||||
chr16:11737175
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255-942C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737175 | ||||||
chr16:11737334
|
T | A | 325 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(322): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.255-1101A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737334 | ||||||
chr16:11737400
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.255-1167C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737400 | ||||||
chr16:11737543
|
C | A | 1 | a0003c0002t0001g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.255-1310G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737543 | ||||||
chr16:11737590
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0122others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-1357C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737590 | ||||||
chr16:11737817
|
C | A | 1 | a0001c0017t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.255-1584G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737817 | ||||||
chr16:11737851
|
C | CA | 39 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(36): Show | 41 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.255-1619dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | ||||||
chr16:11737851
|
C | CAA | 20 | a0001c0001t0001g0128a0001c0004t0001g0001a0001c0004t0001g0006others(17): Show | 23 | HG00408.hp1 HG00544.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.255-1620_255-1619d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | ||||||
chr16:11737851
|
CA | C | 7 | a0001c0001t0001g0267a0002c0003t0001g0141a0002c0003t0001g0142others(4): Show | 7 | HG00323.hp1 HG01070.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.255-1619delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | ||||||
chr16:11738020
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.255-1787C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738020 | ||||||
chr16:11738342
|
A | G | 5 | a0003c0002t0001g0276a0003c0002t0001g0277a0003c0002t0001g0281others(2): Show | 5 | NA18988.hp2 NA19003.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2109T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738342 | ||||||
chr16:11738353
|
A | G | 109 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.255-2120T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738353 | ||||||
chr16:11738407
|
C | G | 1 | a0008c0015t0001g0020 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.255-2174G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738407 | ||||||
chr16:11738436
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.255-2203A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738436 | ||||||
chr16:11738445
|
G | A | 1 | a0002c0003t0001g0197 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.255-2212C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738445 | ||||||
chr16:11738455
|
T | C | 1 | a0010c0026t0001g0265 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.255-2222A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738455 | ||||||
chr16:11738661
|
G | GAA | 26 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0041others(23): Show | 30 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.255-2430_255-2429d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | ||||||
chr16:11738661
|
G | GAAA | 19 | a0001c0004t0001g0025a0001c0004t0001g0026a0001c0004t0001g0061others(16): Show | 20 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.255-2431_255-2429d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | ||||||
chr16:11738661
|
GA | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0123others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.255-2429delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | ||||||
chr16:11738712
|
G | A | 2 | a0004c0006t0001g0003a0004c0006t0001g0351 | 4 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-2479C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738712 | ||||||
chr16:11738875
|
A | G | 1 | a0002c0003t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.255-2642T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738875 | ||||||
chr16:11738989
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.255-2756A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738989 | ||||||
chr16:11739325
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.255-3092C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739325 | ||||||
chr16:11739515
|
C | T | 1 | a0003c0002t0001g0352 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254+2962G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739515 | ||||||
chr16:11739556
|
C | G | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+2921G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739556 | ||||||
chr16:11739600
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0116a0001c0001t0001g0122others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.254+2877G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739600 | ||||||
chr16:11739606
|
A | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.254+2871T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739606 | ||||||
chr16:11739661
|
T | C | 25 | a0001c0001t0001g0111a0001c0004t0001g0001a0001c0004t0001g0006others(22): Show | 28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.254+2816A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739661 | ||||||
chr16:11739762
|
C | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+2715G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739762 | ||||||
chr16:11739796
|
A | G | 81 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 85 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.254+2681T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739796 | ||||||
chr16:11739864
|
T | A | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+2613A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739864 | ||||||
chr16:11740002
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.254+2475C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740002 | ||||||
chr16:11740030
|
G | T | 192 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(189): Show | 205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.254+2447C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740030 | ||||||
chr16:11740146
|
TA | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(51): Show | 60 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.254+2330delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740146 | ||||||
chr16:11740147
|
A | T | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+2330T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740147 | ||||||
chr16:11740228
|
C | CG | 9 | a0001c0001t0001g0072a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG00423.hp1 HG02027.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+2248dupC | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740228 | ||||||
chr16:11740228
|
C | G | 1 | a0015c0016t0001g0021 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.254+2249G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740228 | ||||||
chr16:11740350
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.254+2127G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740350 | ||||||
chr16:11740552
|
T | TA | 3 | a0001c0001t0001g0271a0007c0013t0001g0112a0007c0013t0001g0113 | 3 | HG02145.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.254+1924dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740552 | ||||||
chr16:11740600
|
A | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+1877T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740600 | ||||||
chr16:11740625
|
T | G | 2 | a0001c0004t0001g0025a0001c0004t0001g0026 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.254+1852A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740625 | ||||||
chr16:11740816
|
T | A | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+1661A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740816 | ||||||
chr16:11740931
|
G | A | 14 | a0002c0005t0001g0005a0002c0005t0001g0027a0002c0005t0001g0028others(11): Show | 15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+1546C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740931 | ||||||
chr16:11740965
|
T | C | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+1512A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740965 | ||||||
chr16:11740982
|
T | C | 1 | a0002c0003t0001g0199 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.254+1495A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740982 | ||||||
chr16:11741011
|
T | TA | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+1465dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741011 | ||||||
chr16:11741042
|
A | G | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+1435T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741042 | ||||||
chr16:11741075
|
T | C | 24 | a0001c0004t0001g0001a0001c0004t0001g0006a0001c0004t0001g0040others(21): Show | 27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+1402A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741075 | ||||||
chr16:11741144
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0024t0001g0071 | 3 | NA18988.hp1 NA19075.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.254+1333G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741144 | ||||||
chr16:11741291
|
T | C | 1 | a0003c0002t0001g0352 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254+1186A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741291 | ||||||
chr16:11741353
|
C | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.254+1124G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741353 | ||||||
chr16:11741364
|
G | T | 2 | a0001c0001t0001g0115a0002c0003t0001g0114 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.254+1113C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741364 | ||||||
chr16:11741387
|
G | C | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+1090C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741387 | ||||||
chr16:11741403
|
C | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 55 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.254+1074G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741403 | ||||||
chr16:11741469
|
G | C | 3 | a0006c0010t0001g0272a0006c0010t0001g0273a0006c0010t0001g0274 | 3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.254+1008C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741469 | ||||||
chr16:11741544
|
C | A | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | NA18612.hp2 NA18994.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+933G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741544 | ||||||
chr16:11741659
|
C | G | 1 | a0017c0028t0001g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.254+818G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741659 | ||||||
chr16:11741823
|
A | G | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+654T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741823 | ||||||
chr16:11741867
|
T | C | 2 | a0002c0003t0001g0200a0002c0003t0001g0201 | 2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.254+610A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741867 | ||||||
chr16:11741888
|
C | G | 1 | a0001c0014t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.254+589G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741888 | ||||||
chr16:11741985
|
T | C | 2 | a0002c0011t0001g0062a0002c0011t0001g0063 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+492A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741985 | ||||||
chr16:11742000
|
C | A | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+477G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742000 | ||||||
chr16:11742007
|
G | T | 4 | a0001c0007t0001g0004a0001c0007t0001g0022a0001c0007t0001g0023others(1): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+470C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742007 | ||||||
chr16:11742090
|
C | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 77 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.254+387G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742090 | ||||||
chr16:11742194
|
A | C | 4 | a0002c0003t0002g0064a0002c0003t0002g0065a0002c0003t0002g0066others(1): Show | 4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+283T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742194 | ||||||
chr16:11742232
|
C | T | 6 | a0001c0004t0001g0025a0001c0004t0001g0026a0001c0007t0001g0004others(3): Show | 7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.254+245G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742232 | ||||||
chr16:11742324
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.254+153C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742324 |