geneid | 51060 |
---|---|
ensemblid | ENSG00000117862.13 |
hgncid | 24626 |
symbol | TXNDC12 |
name | thioredoxin domain containing 12 |
refseq_nuc | NM_015913.4 |
refseq_prot | NP_056997.1 |
ensembl_nuc | ENST00000371626.9 |
ensembl_prot | ENSP00000360688.4 |
mane_status | MANE Select |
chr | chr1 |
start | 52020131 |
end | 52055191 |
strand | - |
ver | v1.2 |
region | chr1:52020131-52055191 |
region5000 | chr1:52015131-52060191 |
regionname0 | TXNDC12_chr1_52020131_52055191 |
regionname5000 | TXNDC12_chr1_52015131_52060191 |
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 | 1/1 | 172 | 241 | 81 | 32 | 86 | 6 | 34 | 56 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0002 | 0/0 | 172 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0003 | 0/0 | 172 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
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 | 1/1 | 519 | 237 | 81 | 32 | 82 | 6 | 34 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
c0002 | 0/0 | 519 | 7 | 6 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
c0003 | 0/0 | 519 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
c0004 | 0/0 | 519 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
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 | 1/0 | 898 | 201 | 82 | 28 | 57 | 5 | 28 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
t0002 | 0/0 | 898 | 31 | 0 | 4 | 27 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
t0003 | 0/0 | 898 | 15 | 6 | 1 | 2 | 1 | 5 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
t0004 | 0/1 | 895 | 4 | 1 | 1 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
t0005 | 0/0 | 898 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
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 | 13 | 2 | 4 | 5 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0002 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
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 | 1/1 | 519 | 237 | 81 | 32 | 82 | 6 | 34 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0004 | 0/0 | 519 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0002c0002 | 0/0 | 519 | 7 | 6 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0003c0003 | 0/0 | 519 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1416 | 190 | 73 | 26 | 57 | 5 | 28 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0001t0002 | 0/0 | 1416 | 27 | 0 | 4 | 23 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0001t0003 | 0/0 | 1416 | 15 | 6 | 1 | 2 | 1 | 5 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0001t0004 | 0/1 | 1413 | 4 | 1 | 1 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0001t0005 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0001c0004t0002 | 0/0 | 1416 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0002c0002t0001 | 0/0 | 1416 | 7 | 6 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
a0003c0003t0001 | 0/0 | 1416 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | copy fasta | chr1 | 52015131 | 52060191 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 2 | 4 | 5 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0002 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0004g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0004g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0002c0002t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0003c0003t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
a0003c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | GBR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00423 | hp2 | a0001 | c0004 | t0002 | g0036 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18965 | hp1 | a0001 | c0004 | t0002 | g0035 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18985 | hp1 | a0001 | c0004 | t0002 | g0073 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19010 | hp2 | a0001 | c0004 | t0002 | g0040 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | GIH | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | USA | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | USA | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | USA | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0028 | REF | REF | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | TXNDC12_chr1_52015131_52060191 | TXNDC12 | chr1 | 52015131 | 52060191 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52027321
|
G | A | 1 | a0002 | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
missense_variant | MODERATE | c.239C>T | p.Thr80Met | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/7 | 334/1416 | 239/519 | 80/172 | chr1 | 52027321 | ||
chr1:52055032
|
A | G | 1 | a0003 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
missense_variant | MODERATE | c.65T>C | p.Ile22Thr | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/7 | 160/1416 | 65/519 | 22/172 | chr1 | 52055032 | ||
chr1:52055069
|
T | A | 1 | a0002 | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
missense_variant | MODERATE | c.28A>T | p.Thr10Ser | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/7 | 123/1416 | 28/519 | 10/172 | chr1 | 52055069 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52023513
|
A | G | 1 | a0001c0004 | 4 | HG00423.hp2 NA18965.hp1 NA18985.hp1 others(1): Show |
synonymous_variant | LOW | c.417T>C | p.Tyr139Tyr | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/7 | 512/1416 | 417/519 | 139/172 | chr1 | 52023513 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52020432
|
C | T | 1 | a0001c0001t0003 | 15 | HG00099.hp1 HG01175.hp2 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 7/7 | 501 | chr1 | 52020432 | |||||
chr1:52020491
|
T | C | 2 | a0001c0001t0002a0001c0004t0002 | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*442A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 7/7 | 442 | chr1 | 52020491 | |||||
chr1:52055173
|
G | A | 1 | a0001c0001t0005 | 1 | HG02622.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-77C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/7 | chr1 | 52055173 | ||||||
chr1:52055186
|
CACA | C | 1 | a0001c0001t0004 | 4 | HG01169.hp1 HG02109.hp2 HG04204.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-91delTGT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/7 | 91 | chr1 | 52055186 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52021142
|
C | T | 2 | a0001c0001t0003g0154a0001c0001t0003g0155 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.440-130G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021142 | ||||||
chr1:52021270
|
T | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.440-258A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021270 | ||||||
chr1:52021279
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.440-267G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021279 | ||||||
chr1:52021394
|
C | G | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.440-382G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021394 | ||||||
chr1:52021560
|
C | CA | 22 | a0001c0001t0001g0022a0001c0001t0001g0094a0001c0001t0001g0113others(19): Show | 26 | HG00099.hp1 HG00639.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.440-549dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021560 | ||||||
chr1:52021560
|
CA | C | 26 | a0001c0001t0001g0082a0001c0001t0001g0101a0001c0001t0001g0116others(23): Show | 32 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.440-549delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021560 | ||||||
chr1:52021580
|
A | G | 26 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0006others(23): Show | 32 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.440-568T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021580 | ||||||
chr1:52021790
|
C | T | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-778G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021790 | ||||||
chr1:52021864
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.440-852C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52021864 | ||||||
chr1:52022595
|
T | G | 3 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0195 | 5 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+896A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022595 | ||||||
chr1:52022634
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.439+857C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022634 | ||||||
chr1:52022635
|
G | GT | 53 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056others(50): Show | 62 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.439+855dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022635 | ||||||
chr1:52022635
|
G | GTT | 6 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153others(3): Show | 6 | HG00558.hp2 HG00673.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+854_439+855dup others(2): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022635 | ||||||
chr1:52022637
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0136 | 2 | NA19001.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.439+854A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022637 | ||||||
chr1:52022669
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0161others(29): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.439+822G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022669 | ||||||
chr1:52022765
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 6 | HG02071.hp1 HG02083.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+726G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022765 | ||||||
chr1:52022766
|
G | C | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.439+725C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022766 | ||||||
chr1:52022806
|
A | AT | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+684dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022806 | ||||||
chr1:52022940
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0067others(2): Show | 7 | HG01891.hp2 HG02572.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+551C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52022940 | ||||||
chr1:52023040
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+451G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52023040 | ||||||
chr1:52023202
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.439+289G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52023202 | ||||||
chr1:52023274
|
GT | G | 17 | a0001c0001t0003g0026a0001c0001t0003g0065a0001c0001t0003g0145others(14): Show | 19 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+216delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 6/6 | chr1 | 52023274 | ||||||
chr1:52023595
|
CAG | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.356-23_356-22delCT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023595 | ||||||
chr1:52023649
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.356-75G>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023649 | ||||||
chr1:52023650
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.356-76C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023650 | ||||||
chr1:52023827
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.356-253A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023827 | ||||||
chr1:52023952
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.356-378A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023952 | ||||||
chr1:52023990
|
C | CT | 4 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0167others(1): Show | 8 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-417dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52023990 | ||||||
chr1:52024033
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0141 | 2 | HG01433.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.356-459G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52024033 | ||||||
chr1:52024218
|
T | C | 10 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+292A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52024218 | ||||||
chr1:52024260
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.355+250C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52024260 | ||||||
chr1:52024274
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.355+236C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 5/6 | chr1 | 52024274 | ||||||
chr1:52024609
|
A | G | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-30T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024609 | ||||||
chr1:52024623
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.286-44G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024623 | ||||||
chr1:52024687
|
G | T | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-108C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024687 | ||||||
chr1:52024688
|
C | A | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-109G>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024688 | ||||||
chr1:52024691
|
A | G | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-112T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024691 | ||||||
chr1:52024746
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.286-167G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52024746 | ||||||
chr1:52025271
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.286-692A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025271 | ||||||
chr1:52025287
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.286-708G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025287 | ||||||
chr1:52025288
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.286-709C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025288 | ||||||
chr1:52025292
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0069 | 5 | HG02145.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-713G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025292 | ||||||
chr1:52025483
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0160 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.286-904C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025483 | ||||||
chr1:52025510
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0171 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.286-931C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025510 | ||||||
chr1:52025571
|
C | T | 5 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-992G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025571 | ||||||
chr1:52025642
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.286-1063C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025642 | ||||||
chr1:52025646
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-1067A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025646 | ||||||
chr1:52025699
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.286-1120C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025699 | ||||||
chr1:52025823
|
C | CT | 10 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0144others(7): Show | 12 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-1245dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025823 | ||||||
chr1:52025915
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-1336A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025915 | ||||||
chr1:52025994
|
A | G | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+1281T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52025994 | ||||||
chr1:52026022
|
G | T | 1 | a0001c0004t0002g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.285+1253C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026022 | ||||||
chr1:52026214
|
TGAAAGAG others(5): Show |
T | 1 | a0001c0004t0002g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.285+1049_285+1060d others(14): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026214 | ||||||
chr1:52026762
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.285+513C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026762 | ||||||
chr1:52026853
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0171 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.285+422A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026853 | ||||||
chr1:52026941
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+334G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026941 | ||||||
chr1:52026979
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.285+296G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026979 | ||||||
chr1:52026991
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+284C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026991 | ||||||
chr1:52026994
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0160 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.285+281G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52026994 | ||||||
chr1:52027034
|
TA | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0118a0001c0001t0001g0132others(2): Show | 5 | HG02698.hp2 HG03669.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+240delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 4/6 | chr1 | 52027034 | ||||||
chr1:52027613
|
G | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.212-265C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027613 | ||||||
chr1:52027715
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.212-367G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027715 | ||||||
chr1:52027740
|
T | TATATATA others(1): Show |
24 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(21): Show | 30 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.212-400_212-393dup others(8): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027740 | ||||||
chr1:52027779
|
TTA | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-433_212-432del others(2): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027779 | ||||||
chr1:52027866
|
T | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0044others(4): Show | 10 | HG00544.hp2 HG02027.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-518A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027866 | ||||||
chr1:52027925
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.212-577G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52027925 | ||||||
chr1:52028116
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.211+462G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028116 | ||||||
chr1:52028139
|
T | G | 2 | a0001c0001t0003g0157a0001c0001t0003g0166 | 2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.211+439A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028139 | ||||||
chr1:52028362
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+216G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028362 | ||||||
chr1:52028454
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+124T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028454 | ||||||
chr1:52028460
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211+118G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028460 | ||||||
chr1:52028485
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.211+93T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 3/6 | chr1 | 52028485 | ||||||
chr1:52028745
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-115T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52028745 | ||||||
chr1:52028863
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.159-233G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52028863 | ||||||
chr1:52028882
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.159-252G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52028882 | ||||||
chr1:52028907
|
G | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.159-277C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52028907 | ||||||
chr1:52028998
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0078 | 2 | NA18959.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.159-368G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52028998 | ||||||
chr1:52029569
|
T | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0043others(1): Show | 6 | HG00609.hp1 HG02040.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-939A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52029569 | ||||||
chr1:52029851
|
T | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.159-1221A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52029851 | ||||||
chr1:52029943
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.159-1313A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52029943 | ||||||
chr1:52029952
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.159-1322C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52029952 | ||||||
chr1:52030271
|
T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0143others(70): Show | 89 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.159-1641A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52030271 | ||||||
chr1:52030377
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.159-1747T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52030377 | ||||||
chr1:52030573
|
T | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.159-1943A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52030573 | ||||||
chr1:52030685
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.159-2055G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52030685 | ||||||
chr1:52031160
|
C | CT | 18 | a0001c0001t0001g0025a0001c0001t0001g0080a0001c0001t0001g0081others(15): Show | 20 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.159-2531dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031160 | ||||||
chr1:52031160
|
CT | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0104others(29): Show | 42 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.159-2531delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031160 | ||||||
chr1:52031263
|
G | A | 1 | a0002c0002t0001g0014 | 3 | HG00639.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.159-2633C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031263 | ||||||
chr1:52031306
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.159-2676G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031306 | ||||||
chr1:52031316
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.159-2686G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031316 | ||||||
chr1:52031405
|
G | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-2775C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031405 | ||||||
chr1:52031405
|
G | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.159-2775C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031405 | ||||||
chr1:52031586
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159-2956T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031586 | ||||||
chr1:52031602
|
C | T | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-2972G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031602 | ||||||
chr1:52031775
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.159-3145C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031775 | ||||||
chr1:52031805
|
A | T | 5 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-3175T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031805 | ||||||
chr1:52031946
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.159-3316G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52031946 | ||||||
chr1:52032186
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-3556A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032186 | ||||||
chr1:52032372
|
C | G | 1 | a0001c0001t0003g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159-3742G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032372 | ||||||
chr1:52032440
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-3810G>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032440 | ||||||
chr1:52032465
|
T | TG | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.159-3836dupC | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032465 | ||||||
chr1:52032474
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.159-3844A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032474 | ||||||
chr1:52032657
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0079a0001c0001t0001g0085others(2): Show | 6 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-4027A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032657 | ||||||
chr1:52032698
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0074others(72): Show | 91 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.159-4068G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032698 | ||||||
chr1:52032900
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.159-4270G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52032900 | ||||||
chr1:52033049
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-4419C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033049 | ||||||
chr1:52033061
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.159-4431G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033061 | ||||||
chr1:52033189
|
A | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.159-4559T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033189 | ||||||
chr1:52033386
|
G | C | 2 | a0001c0001t0003g0154a0001c0001t0003g0155 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.159-4756C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033386 | ||||||
chr1:52033398
|
CGCCCGCC others(20): Show |
C | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-4795_159-4769d others(29): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033398 | ||||||
chr1:52033427
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.159-4797G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033427 | ||||||
chr1:52033437
|
G | T | 1 | a0001c0001t0002g0078 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.159-4807C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033437 | ||||||
chr1:52033510
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.159-4880C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033510 | ||||||
chr1:52033787
|
C | A | 5 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-5157G>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033787 | ||||||
chr1:52033817
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-5187C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033817 | ||||||
chr1:52033890
|
T | A | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-5260A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033890 | ||||||
chr1:52033917
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.159-5287C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52033917 | ||||||
chr1:52034267
|
G | A | 17 | a0001c0001t0003g0026a0001c0001t0003g0065a0001c0001t0003g0145others(14): Show | 19 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-5637C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034267 | ||||||
chr1:52034448
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.159-5818A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034448 | ||||||
chr1:52034642
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-6012C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034642 | ||||||
chr1:52034743
|
G | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.159-6113C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034743 | ||||||
chr1:52034766
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.159-6136T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034766 | ||||||
chr1:52034812
|
G | C | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-6182C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034812 | ||||||
chr1:52034814
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.159-6184T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034814 | ||||||
chr1:52034844
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.159-6214T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52034844 | ||||||
chr1:52035232
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+6305C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035232 | ||||||
chr1:52035480
|
G | A | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.158+6057C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035480 | ||||||
chr1:52035491
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.158+6046C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035491 | ||||||
chr1:52035561
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158+5976T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035561 | ||||||
chr1:52035636
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0168 | 2 | NA18906.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.158+5901G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035636 | ||||||
chr1:52035680
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+5857G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035680 | ||||||
chr1:52035832
|
A | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.158+5705T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035832 | ||||||
chr1:52035859
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.158+5678A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035859 | ||||||
chr1:52035866
|
T | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.158+5671A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035866 | ||||||
chr1:52035965
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+5572G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52035965 | ||||||
chr1:52036253
|
T | TTA | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.158+5282_158+5283d others(4): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036253 | ||||||
chr1:52036375
|
T | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.158+5162A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036375 | ||||||
chr1:52036644
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158+4893C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036644 | ||||||
chr1:52036713
|
A | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.158+4824T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036713 | ||||||
chr1:52036803
|
C | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0096a0001c0001t0001g0126 | 3 | HG03195.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.158+4734G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036803 | ||||||
chr1:52036826
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 6 | HG02071.hp1 HG02083.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+4711A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036826 | ||||||
chr1:52036839
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.158+4698A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036839 | ||||||
chr1:52036862
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.158+4675G>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52036862 | ||||||
chr1:52037038
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.158+4499G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037038 | ||||||
chr1:52037043
|
T | C | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.158+4494A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037043 | ||||||
chr1:52037207
|
C | CT | 29 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0055others(26): Show | 32 | HG00544.hp1 HG00558.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.158+4329dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037207 | ||||||
chr1:52037207
|
CT | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0001g0121others(3): Show | 9 | HG00639.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+4329delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037207 | ||||||
chr1:52037207
|
CTTT | C | 23 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(20): Show | 29 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.158+4327_158+4329d others(5): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037207 | ||||||
chr1:52037207
|
CTTTT | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0078others(1): Show | 8 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+4326_158+4329d others(6): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037207 | ||||||
chr1:52037312
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.158+4225T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037312 | ||||||
chr1:52037326
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+4211G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037326 | ||||||
chr1:52037463
|
C | T | 1 | a0002c0002t0001g0014 | 3 | HG00639.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.158+4074G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037463 | ||||||
chr1:52037510
|
C | T | 5 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+4027G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037510 | ||||||
chr1:52037740
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.158+3797G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037740 | ||||||
chr1:52037790
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158+3747G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037790 | ||||||
chr1:52037931
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.158+3606A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52037931 | ||||||
chr1:52038128
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.158+3409A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038128 | ||||||
chr1:52038187
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18955.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.158+3350A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038187 | ||||||
chr1:52038315
|
G | GT | 37 | a0001c0001t0001g0127a0001c0001t0002g0004a0001c0001t0002g0006others(34): Show | 44 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.158+3221dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038315 | ||||||
chr1:52038315
|
GT | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(12): Show | 19 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.158+3221delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038315 | ||||||
chr1:52038380
|
C | T | 2 | a0001c0001t0003g0154a0001c0001t0003g0155 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.158+3157G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038380 | ||||||
chr1:52038504
|
G | T | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.158+3033C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038504 | ||||||
chr1:52038531
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.158+3006A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038531 | ||||||
chr1:52038785
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+2752A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038785 | ||||||
chr1:52038903
|
GT | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 184 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.158+2633delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038903 | ||||||
chr1:52038903
|
GTT | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(23): Show | 36 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.158+2632_158+2633d others(4): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52038903 | ||||||
chr1:52039045
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158+2492A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039045 | ||||||
chr1:52039088
|
C | CA | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 198 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.158+2448dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039088 | ||||||
chr1:52039088
|
C | CAA | 12 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0084others(9): Show | 12 | HG01261.hp1 HG01261.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.158+2447_158+2448d others(4): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039088 | ||||||
chr1:52039088
|
C | CAAAAA | 18 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(15): Show | 24 | HG00423.hp2 HG00609.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.158+2444_158+2448d others(7): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039088 | ||||||
chr1:52039088
|
C | CAAAAAA | 9 | a0001c0001t0001g0002a0001c0001t0002g0031a0001c0001t0002g0033others(6): Show | 13 | HG00544.hp2 HG00673.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.158+2443_158+2448d others(8): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039088 | ||||||
chr1:52039190
|
TTGTAA | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0070 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.158+2342_158+2346d others(7): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039190 | ||||||
chr1:52039237
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158+2300G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039237 | ||||||
chr1:52039333
|
A | AT | 8 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0168others(5): Show | 10 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.158+2203dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039333 | ||||||
chr1:52039333
|
AT | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0167others(27): Show | 40 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.158+2203delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039333 | ||||||
chr1:52039477
|
G | A | 13 | a0001c0001t0002g0017a0001c0001t0002g0031a0001c0001t0002g0033others(10): Show | 14 | HG00423.hp2 HG00673.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.158+2060C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039477 | ||||||
chr1:52039613
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+1924C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039613 | ||||||
chr1:52039640
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.158+1897G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039640 | ||||||
chr1:52039650
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.158+1887G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039650 | ||||||
chr1:52039674
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.158+1863C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039674 | ||||||
chr1:52039693
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0160 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.158+1844T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039693 | ||||||
chr1:52039748
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.158+1789A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039748 | ||||||
chr1:52039774
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0051others(9): Show | 17 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+1763T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52039774 | ||||||
chr1:52040034
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0143others(65): Show | 82 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.158+1503A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040034 | ||||||
chr1:52040476
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.158+1061G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040476 | ||||||
chr1:52040650
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158+887A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040650 | ||||||
chr1:52040697
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+840A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040697 | ||||||
chr1:52040810
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.158+727G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040810 | ||||||
chr1:52040821
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.158+716C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040821 | ||||||
chr1:52040959
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.158+578A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52040959 | ||||||
chr1:52041070
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0067others(2): Show | 7 | HG01891.hp2 HG02572.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+467G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041070 | ||||||
chr1:52041195
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.158+342A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041195 | ||||||
chr1:52041207
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.158+330G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041207 | ||||||
chr1:52041338
|
G | GA | 5 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0086others(2): Show | 5 | HG01167.hp1 NA18980.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+198dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041338 | ||||||
chr1:52041338
|
GA | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 10 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+198delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041338 | ||||||
chr1:52041398
|
T | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0074others(72): Show | 91 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.158+139A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041398 | ||||||
chr1:52041489
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.158+48G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 2/6 | chr1 | 52041489 | ||||||
chr1:52041615
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.98-18A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52041615 | ||||||
chr1:52041662
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0171 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.98-65A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52041662 | ||||||
chr1:52041719
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0122a0001c0001t0001g0133 | 5 | HG02132.hp2 NA18612.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-122A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52041719 | ||||||
chr1:52041846
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-249C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52041846 | ||||||
chr1:52041969
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.98-372T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52041969 | ||||||
chr1:52042022
|
G | A | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-425C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042022 | ||||||
chr1:52042189
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98-592G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042189 | ||||||
chr1:52042199
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0171 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.98-602A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042199 | ||||||
chr1:52042464
|
C | CT | 28 | a0001c0001t0001g0020a0001c0001t0001g0091a0001c0001t0001g0108others(25): Show | 33 | HG00423.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-868dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042464 | ||||||
chr1:52042464
|
CT | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0143a0001c0001t0001g0170others(3): Show | 6 | HG02055.hp1 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-868delA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042464 | ||||||
chr1:52042464
|
CTT | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.98-869_98-868delAA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042464 | ||||||
chr1:52042526
|
T | G | 17 | a0001c0001t0003g0026a0001c0001t0003g0065a0001c0001t0003g0145others(14): Show | 19 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-929A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042526 | ||||||
chr1:52042850
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0095 | 3 | HG02602.hp2 HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.98-1253C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042850 | ||||||
chr1:52042917
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.98-1320G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042917 | ||||||
chr1:52042979
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.98-1382G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52042979 | ||||||
chr1:52043056
|
C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-1459G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043056 | ||||||
chr1:52043286
|
T | C | 8 | a0001c0001t0003g0026a0001c0001t0003g0156a0001c0001t0003g0157others(5): Show | 9 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-1689A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043286 | ||||||
chr1:52043394
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.98-1797C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043394 | ||||||
chr1:52043469
|
T | G | 1 | a0001c0001t0001g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1872A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043469 | ||||||
chr1:52043503
|
A | G | 4 | a0001c0001t0003g0065a0001c0001t0003g0147a0001c0001t0003g0154others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1906T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043503 | ||||||
chr1:52043511
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.98-1914A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043511 | ||||||
chr1:52043601
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.98-2004C>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043601 | ||||||
chr1:52043737
|
G | C | 5 | a0002c0002t0001g0014a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 7 | HG00639.hp2 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-2140C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043737 | ||||||
chr1:52043897
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0160 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.98-2300T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52043897 | ||||||
chr1:52044042
|
T | C | 14 | a0001c0001t0003g0026a0001c0001t0003g0065a0001c0001t0003g0145others(11): Show | 15 | HG00099.hp1 HG01175.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-2445A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044042 | ||||||
chr1:52044337
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.98-2740T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044337 | ||||||
chr1:52044358
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0004g0028 | 6 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-2761C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044358 | ||||||
chr1:52044358
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.98-2761C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044358 | ||||||
chr1:52044719
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.98-3122T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044719 | ||||||
chr1:52044919
|
G | A | 10 | a0001c0001t0003g0026a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 11 | HG00099.hp1 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-3322C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044919 | ||||||
chr1:52044974
|
C | CA | 10 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0161others(7): Show | 12 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-3378dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044974 | ||||||
chr1:52044974
|
CA | C | 6 | a0001c0001t0001g0103a0001c0001t0001g0172a0001c0001t0002g0006others(3): Show | 8 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-3378delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52044974 | ||||||
chr1:52045164
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.98-3567A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52045164 | ||||||
chr1:52045589
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.98-3992T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52045589 | ||||||
chr1:52045645
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0171 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.98-4048T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52045645 | ||||||
chr1:52045750
|
C | T | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-4153G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52045750 | ||||||
chr1:52046035
|
A | C | 1 | a0001c0001t0002g0042 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.98-4438T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046035 | ||||||
chr1:52046111
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-4514C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046111 | ||||||
chr1:52046146
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.98-4549G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046146 | ||||||
chr1:52046199
|
G | GA | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.98-4603dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046199 | ||||||
chr1:52046604
|
C | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.98-5007G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046604 | ||||||
chr1:52046701
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 6 | HG02647.hp1 HG02818.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-5104C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046701 | ||||||
chr1:52046744
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.98-5147C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046744 | ||||||
chr1:52046799
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0004g0028 | 6 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-5202G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046799 | ||||||
chr1:52046853
|
TAAAA | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0081a0001c0001t0001g0082others(10): Show | 15 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.98-5260_98-5257del others(4): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046853 | ||||||
chr1:52046853
|
TAAAAAA | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0091others(4): Show | 9 | HG00423.hp1 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-5262_98-5257del others(6): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046853 | ||||||
chr1:52046862
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.98-5266_98-5265ins others(10): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046862 | ||||||
chr1:52046862
|
AAAAAAT | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(44): Show | 71 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.98-5271_98-5266del others(6): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046862 | ||||||
chr1:52046863
|
AAAAAT | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0125a0001c0001t0001g0160others(2): Show | 6 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-5271_98-5267del others(5): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046863 | ||||||
chr1:52046864
|
A | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5267T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046864 | ||||||
chr1:52046864
|
AAAATAT | A | 19 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 24 | HG01433.hp2 HG01515.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.98-5273_98-5268del others(6): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046864 | ||||||
chr1:52046865
|
AAATATAT | A | 11 | a0001c0001t0001g0134a0001c0001t0003g0026a0001c0001t0003g0145others(8): Show | 12 | HG01175.hp2 HG02109.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-5275_98-5269del others(7): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046865 | ||||||
chr1:52046866
|
A | AAAATATA others(3): Show |
3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02055.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.98-5270_98-5269ins others(10): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
A | AAATATAT | 10 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0032others(7): Show | 15 | HG00544.hp2 HG00609.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-5270_98-5269ins others(7): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
A | AATATATA others(1): Show |
8 | a0001c0001t0002g0017a0001c0001t0002g0034a0001c0001t0002g0038others(5): Show | 9 | HG00673.hp1 HG01928.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-5277_98-5270dup others(8): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
A | AATATATA others(3): Show |
3 | a0001c0001t0002g0037a0001c0004t0002g0035a0001c0004t0002g0036 | 3 | HG00423.hp2 NA18965.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.98-5279_98-5270dup others(10): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.98-5270_98-5269ins others(11): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
A | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0140others(3): Show | 6 | HG01261.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-5269T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
AAT | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 13 | HG01109.hp1 HG01167.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-5271_98-5270del others(2): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
AATATAT | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0161others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-5275_98-5270del others(6): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046866
|
AATATATA others(1): Show |
A | 14 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(11): Show | 18 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.98-5277_98-5270del others(8): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046866 | ||||||
chr1:52046867
|
ATAT | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0051others(8): Show | 16 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.98-5273_98-5271del others(3): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046867 | ||||||
chr1:52046867
|
ATATAT | A | 2 | a0001c0001t0001g0002a0001c0001t0004g0028 | 6 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-5275_98-5271del others(5): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046867 | ||||||
chr1:52046870
|
T | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG01109.hp1 HG01167.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-5273A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046870 | ||||||
chr1:52046872
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.98-5275A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046872 | ||||||
chr1:52046874
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-5277A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046874 | ||||||
chr1:52046876
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0153a0001c0001t0004g0028 | 7 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-5279A>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52046876 | ||||||
chr1:52047060
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0004g0028 | 7 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-5463C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047060 | ||||||
chr1:52047179
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98-5582G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047179 | ||||||
chr1:52047314
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.98-5717G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047314 | ||||||
chr1:52047372
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.98-5775T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047372 | ||||||
chr1:52047508
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.98-5911G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047508 | ||||||
chr1:52047512
|
G | A | 1 | a0001c0001t0003g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98-5915C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047512 | ||||||
chr1:52047730
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.98-6133G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047730 | ||||||
chr1:52047759
|
C | CA | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.98-6163dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047759 | ||||||
chr1:52047830
|
A | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-6233T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52047830 | ||||||
chr1:52048071
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.98-6474A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048071 | ||||||
chr1:52048212
|
C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-6615G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048212 | ||||||
chr1:52048298
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01167.hp1 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-6701G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048298 | ||||||
chr1:52048398
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0051others(34): Show | 48 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.97+6602G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048398 | ||||||
chr1:52048399
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.97+6601C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048399 | ||||||
chr1:52048473
|
T | TA | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0161others(2): Show | 5 | HG01433.hp2 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6526dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048473 | ||||||
chr1:52048473
|
TA | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 14 | HG00558.hp2 HG01109.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+6526delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048473 | ||||||
chr1:52048500
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18955.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.97+6500T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048500 | ||||||
chr1:52048533
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.97+6467T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048533 | ||||||
chr1:52048673
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97+6327G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048673 | ||||||
chr1:52048723
|
G | A | 1 | a0002c0002t0001g0014 | 3 | HG00639.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97+6277C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048723 | ||||||
chr1:52048866
|
A | AT | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.97+6133dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52048866 | ||||||
chr1:52049543
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97+5457C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049543 | ||||||
chr1:52049553
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+5447A>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049553 | ||||||
chr1:52049704
|
A | AT | 30 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0167others(27): Show | 40 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.97+5295dupA | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049704 | ||||||
chr1:52049780
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.97+5220A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049780 | ||||||
chr1:52049891
|
C | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 10 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+5109G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049891 | ||||||
chr1:52049945
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.97+5055T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049945 | ||||||
chr1:52049957
|
C | T | 14 | a0001c0001t0003g0026a0001c0001t0003g0065a0001c0001t0003g0145others(11): Show | 15 | HG00099.hp1 HG01175.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.97+5043G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049957 | ||||||
chr1:52049969
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0164 | 2 | NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.97+5031C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52049969 | ||||||
chr1:52050186
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.97+4814G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050186 | ||||||
chr1:52050619
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.97+4381C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050619 | ||||||
chr1:52050652
|
A | G | 1 | a0001c0001t0002g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.97+4348T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050652 | ||||||
chr1:52050716
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+4284A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050716 | ||||||
chr1:52050967
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0001g0072 | 5 | HG01891.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+4033A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050967 | ||||||
chr1:52050980
|
G | C | 1 | a0001c0001t0003g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.97+4020C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52050980 | ||||||
chr1:52051254
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0148others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+3746G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051254 | ||||||
chr1:52051299
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.97+3701A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051299 | ||||||
chr1:52051372
|
AATTT | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18955.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.97+3624_97+3627del others(4): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051372 | ||||||
chr1:52051380
|
TA | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0032others(1): Show | 8 | HG02145.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+3619delT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051380 | ||||||
chr1:52051381
|
A | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(21): Show | 30 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.97+3619T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051381 | ||||||
chr1:52051385
|
A | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0002g0004others(25): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.97+3615T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051385 | ||||||
chr1:52051460
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+3540G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051460 | ||||||
chr1:52051525
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.97+3475C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051525 | ||||||
chr1:52051561
|
T | C | 1 | a0002c0002t0001g0014 | 3 | HG00639.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97+3439A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051561 | ||||||
chr1:52051740
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.97+3260T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52051740 | ||||||
chr1:52052132
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 218 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.97+2868A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52052132 | ||||||
chr1:52052492
|
A | G | 25 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(22): Show | 31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.97+2508T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52052492 | ||||||
chr1:52052888
|
G | C | 1 | a0001c0001t0003g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.97+2112C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52052888 | ||||||
chr1:52053099
|
C | CA | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(93): Show | 129 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.97+1900dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053099 | ||||||
chr1:52053099
|
C | CAA | 60 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(57): Show | 72 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.97+1899_97+1900dup others(2): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053099 | ||||||
chr1:52053099
|
C | CAAA | 34 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0066others(31): Show | 45 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.97+1898_97+1900dup others(3): Show |
TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053099 | ||||||
chr1:52053188
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+1812C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053188 | ||||||
chr1:52053321
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.97+1679G>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053321 | ||||||
chr1:52053329
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+1671T>C | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053329 | ||||||
chr1:52053356
|
A | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(92): Show | 128 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.97+1644T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053356 | ||||||
chr1:52053385
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.97+1615G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053385 | ||||||
chr1:52053563
|
C | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(21): Show | 30 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.97+1437G>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053563 | ||||||
chr1:52053620
|
T | C | 1 | a0002c0002t0001g0014 | 3 | HG00639.hp2 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97+1380A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053620 | ||||||
chr1:52053681
|
A | C | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1319T>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053681 | ||||||
chr1:52053685
|
C | CA | 17 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.97+1314dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52053685 | ||||||
chr1:52054150
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.97+850T>A | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054150 | ||||||
chr1:52054156
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.97+844C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054156 | ||||||
chr1:52054216
|
G | GA | 13 | a0001c0001t0001g0003a0001c0001t0001g0179a0001c0001t0001g0180others(10): Show | 17 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.97+783dupT | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054216 | ||||||
chr1:52054258
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 189 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.97+742A>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054258 | ||||||
chr1:52054507
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.97+493C>G | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054507 | ||||||
chr1:52054931
|
G | A | 3 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0030 | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+69C>T | TXNDC12 | ENSG00000117862.13 | transcript | ENST00000371626.9 | protein_coding | 1/6 | chr1 | 52054931 |