geneid | 7148 |
---|---|
ensemblid | ENSG00000168477.21 |
hgncid | 11976 |
symbol | TNXB |
name | tenascin XB |
refseq_nuc | NM_001365276.2 |
refseq_prot | NP_001352205.1 |
ensembl_nuc | ENST00000644971.2 |
ensembl_prot | ENSP00000496448.1 |
mane_status | MANE Select |
chr | chr6 |
start | 32041153 |
end | 32109338 |
strand | - |
ver | v1.2 |
region | chr6:32041153-32109338 |
region5000 | chr6:32036153-32114338 |
regionname0 | TNXB_chr6_32041153_32109338 |
regionname5000 | TNXB_chr6_32036153_32114338 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 4244 | 63 | 1 | 18 | 36 | 3 | 4 | 32 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002 | 0/0 | 4244 | 45 | 3 | 10 | 29 | 0 | 3 | 24 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003 | 0/0 | 4244 | 22 | 0 | 0 | 22 | 0 | 0 | 14 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004 | 0/0 | 4244 | 20 | 11 | 4 | 4 | 0 | 1 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005 | 0/0 | 4244 | 17 | 0 | 1 | 16 | 0 | 0 | 14 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0006 | 0/0 | 4244 | 14 | 8 | 6 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0007 | 0/0 | 4244 | 14 | 1 | 0 | 13 | 0 | 0 | 13 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0008 | 0/0 | 4244 | 14 | 6 | 0 | 2 | 2 | 4 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009 | 0/0 | 4244 | 11 | 6 | 0 | 5 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010 | 0/0 | 4244 | 11 | 5 | 4 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0011 | 0/0 | 4244 | 10 | 2 | 4 | 1 | 1 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0012 | 0/0 | 4244 | 7 | 4 | 0 | 2 | 0 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0013 | 0/0 | 4244 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0014 | 0/0 | 4244 | 6 | 0 | 3 | 2 | 1 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0015 | 0/0 | 4244 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0016 | 0/0 | 4244 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0017 | 0/0 | 4133 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0018 | 0/0 | 4244 | 5 | 1 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0019 | 0/0 | 4244 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0020 | 0/0 | 4244 | 4 | 1 | 0 | 3 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0021 | 0/0 | 4244 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0022 | 0/0 | 4244 | 4 | 0 | 0 | 2 | 0 | 2 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0023 | 0/0 | 4244 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0024 | 0/0 | 4244 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0025 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0026 | 0/0 | 4244 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0027 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0028 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0029 | 0/0 | 4244 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0030 | 0/0 | 4244 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0031 | 0/0 | 4244 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0032 | 0/0 | 4244 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0033 | 0/0 | 4244 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0034 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0035 | 0/0 | 4244 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0036 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0037 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0038 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0039 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0040 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0041 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0042 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0043 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0044 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0045 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0046 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0047 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0048 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0049 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0050 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0051 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0052 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0053 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0054 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0055 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0056 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0057 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0058 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0059 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0060 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0061 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0062 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0063 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0064 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0065 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0066 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0067 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0068 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0069 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0070 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0071 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0072 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0073 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0074 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0075 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0076 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0077 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0078 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0079 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0080 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0081 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0082 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0083 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0084 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0085 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0086 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0087 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0088 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0089 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0090 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0091 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0092 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0093 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0094 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0095 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0096 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0097 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0098 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0099 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 12735 | 46 | 0 | 14 | 26 | 2 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0002 | 0/0 | 12735 | 27 | 0 | 2 | 22 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0003 | 0/0 | 12735 | 19 | 0 | 0 | 19 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0004 | 0/0 | 12735 | 14 | 8 | 6 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0005 | 0/0 | 12735 | 14 | 1 | 0 | 13 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0006 | 0/0 | 12735 | 12 | 5 | 0 | 2 | 1 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0007 | 0/0 | 12735 | 12 | 0 | 3 | 8 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0008 | 0/0 | 12735 | 10 | 8 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0009 | 0/0 | 12735 | 10 | 2 | 4 | 1 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0010 | 0/0 | 12735 | 10 | 4 | 4 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0011 | 0/0 | 12735 | 9 | 2 | 2 | 4 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0012 | 0/0 | 12735 | 8 | 0 | 3 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0013 | 0/0 | 12735 | 7 | 0 | 0 | 7 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0014 | 0/0 | 12735 | 6 | 0 | 1 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0015 | 0/0 | 12735 | 6 | 3 | 0 | 2 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0016 | 0/0 | 12735 | 6 | 0 | 0 | 6 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0017 | 0/0 | 12735 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0018 | 0/0 | 12735 | 5 | 0 | 3 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0019 | 0/0 | 12735 | 5 | 0 | 5 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0020 | 0/0 | 12735 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0021 | 0/0 | 12735 | 5 | 1 | 4 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0022 | 0/0 | 12402 | 5 | 5 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0023 | 0/0 | 12735 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0024 | 0/0 | 12735 | 5 | 0 | 1 | 4 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0025 | 0/0 | 12735 | 4 | 1 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0026 | 0/0 | 12735 | 4 | 0 | 0 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0027 | 0/0 | 12735 | 4 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0028 | 0/0 | 12735 | 4 | 0 | 3 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0029 | 0/0 | 12735 | 3 | 0 | 0 | 1 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0030 | 0/0 | 12735 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0031 | 0/0 | 12735 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0032 | 0/0 | 12735 | 3 | 0 | 2 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0033 | 0/0 | 12735 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0034 | 0/0 | 12735 | 3 | 1 | 1 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0035 | 0/0 | 12735 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0036 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0037 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0038 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0039 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0040 | 0/0 | 12735 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0041 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0042 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0043 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0044 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0045 | 0/0 | 12735 | 2 | 1 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0046 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0047 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0048 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0049 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0050 | 0/0 | 12735 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0051 | 0/0 | 12735 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0052 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0053 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0054 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0055 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0056 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0057 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0058 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0059 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0060 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0061 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0062 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0063 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0064 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0065 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0066 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0067 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0068 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0069 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0070 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0071 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0072 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0073 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0074 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0075 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0076 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0077 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0078 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0079 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0080 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0081 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0082 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0083 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0084 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0085 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0086 | 0/0 | 12750 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0087 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0088 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0089 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0090 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0091 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0092 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0093 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0094 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0095 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0096 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0097 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0098 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0099 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0100 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0101 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0102 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0103 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0104 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0105 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0106 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0107 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0108 | 0/0 | 12645 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0109 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0110 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0111 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0112 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0113 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0114 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0115 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0116 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0117 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0118 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0119 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0120 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0121 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0122 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0123 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0124 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0125 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
c0126 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 363 | 244 | 55 | 39 | 115 | 7 | 27 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0002 | 0/0 | 363 | 146 | 29 | 34 | 61 | 10 | 12 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0003 | 0/0 | 363 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0004 | 0/0 | 363 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0005 | 0/0 | 363 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0006 | 0/0 | 363 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
t0007 | 0/0 | 363 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 12735 | 46 | 0 | 14 | 26 | 2 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0007 | 0/0 | 12735 | 12 | 0 | 3 | 8 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0034 | 0/0 | 12735 | 3 | 1 | 1 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0109 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0110 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0002 | 0/0 | 12735 | 27 | 0 | 2 | 22 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0012 | 0/0 | 12735 | 8 | 0 | 3 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0019 | 0/0 | 12735 | 5 | 0 | 5 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0042 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0094 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0096 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0097 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0003 | 0/0 | 12735 | 19 | 0 | 0 | 19 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0048 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0113 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0008 | 0/0 | 12735 | 10 | 8 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0011 | 0/0 | 12735 | 9 | 2 | 2 | 4 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0062 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0013 | 0/0 | 12735 | 7 | 0 | 0 | 7 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0023 | 0/0 | 12735 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0024 | 0/0 | 12735 | 5 | 0 | 1 | 4 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0006c0004 | 0/0 | 12735 | 14 | 8 | 6 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0007c0005 | 0/0 | 12735 | 14 | 1 | 0 | 13 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0008c0006 | 0/0 | 12735 | 12 | 5 | 0 | 2 | 1 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0008c0045 | 0/0 | 12735 | 2 | 1 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0020 | 0/0 | 12735 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0027 | 0/0 | 12735 | 4 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0070 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0092 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010c0010 | 0/0 | 12735 | 10 | 4 | 4 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010c0084 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0011c0009 | 0/0 | 12735 | 10 | 2 | 4 | 1 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0012c0015 | 0/0 | 12735 | 6 | 3 | 0 | 2 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0012c0099 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0013c0014 | 0/0 | 12735 | 6 | 0 | 1 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0014c0018 | 0/0 | 12735 | 5 | 0 | 3 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0014c0081 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0015c0016 | 0/0 | 12735 | 6 | 0 | 0 | 6 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0016c0017 | 0/0 | 12735 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0017c0022 | 0/0 | 12402 | 5 | 5 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0018c0021 | 0/0 | 12735 | 5 | 1 | 4 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0019c0028 | 0/0 | 12735 | 4 | 0 | 3 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0020c0025 | 0/0 | 12735 | 4 | 1 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0021c0026 | 0/0 | 12735 | 4 | 0 | 0 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0022c0029 | 0/0 | 12735 | 3 | 0 | 0 | 1 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0022c0059 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0023c0036 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0023c0053 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0024c0032 | 0/0 | 12735 | 3 | 0 | 2 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0025c0037 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0025c0069 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0026c0033 | 0/0 | 12735 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0027c0052 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0027c0125 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0028c0035 | 0/0 | 12735 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0029c0030 | 0/0 | 12735 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0030c0031 | 0/0 | 12735 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0031c0051 | 0/0 | 12735 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0032c0050 | 0/0 | 12735 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0033c0043 | 0/0 | 12735 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0034c0039 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0035c0040 | 0/0 | 12735 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0036c0038 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0037c0041 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0038c0044 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0039c0046 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0040c0047 | 0/0 | 12735 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0041c0049 | 0/0 | 12735 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0042c0054 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0043c0055 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0044c0061 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0045c0063 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0046c0126 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0047c0065 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0048c0066 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0049c0068 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0050c0067 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0051c0120 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0052c0121 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0053c0119 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0054c0122 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0055c0123 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0056c0118 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0057c0071 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0058c0073 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0059c0074 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0060c0117 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0061c0077 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0062c0076 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0063c0098 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0064c0079 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0065c0093 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0066c0091 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0067c0082 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0068c0095 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0069c0083 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0070c0090 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0071c0089 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0072c0086 | 0/0 | 12750 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0073c0087 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0074c0088 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0075c0085 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0076c0080 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0077c0078 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0078c0075 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0079c0100 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0080c0101 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0081c0102 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0082c0112 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0083c0108 | 0/0 | 12645 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0084c0107 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0085c0106 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0086c0111 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0087c0105 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0088c0104 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0089c0103 | 0/0 | 12735 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0090c0115 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0091c0114 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0092c0072 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0093c0116 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0094c0124 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0095c0064 | 0/0 | 12735 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0096c0057 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0097c0058 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0098c0056 | 0/0 | 12735 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0099c0060 | 0/0 | 12735 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 13097 | 45 | 0 | 14 | 26 | 1 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0001t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0007t0001 | 0/0 | 13097 | 12 | 0 | 3 | 8 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0034t0001 | 0/0 | 13097 | 3 | 1 | 1 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0109t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0001c0110t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0002t0001 | 0/0 | 13097 | 27 | 0 | 2 | 22 | 0 | 3 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0012t0002 | 0/0 | 13097 | 8 | 0 | 3 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0019t0002 | 0/0 | 13097 | 5 | 0 | 5 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0042t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0094t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0096t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0002c0097t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0003t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0003t0002 | 0/0 | 13097 | 18 | 0 | 0 | 18 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0048t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0048t0005 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0003c0113t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0008t0001 | 0/0 | 13097 | 10 | 8 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0011t0001 | 0/0 | 13097 | 9 | 2 | 2 | 4 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0004c0062t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0013t0001 | 0/0 | 13097 | 7 | 0 | 0 | 7 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0023t0001 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0005c0024t0001 | 0/0 | 13097 | 5 | 0 | 1 | 4 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0006c0004t0001 | 0/0 | 13097 | 14 | 8 | 6 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0007c0005t0002 | 0/0 | 13097 | 14 | 1 | 0 | 13 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0008c0006t0001 | 0/0 | 13097 | 12 | 5 | 0 | 2 | 1 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0008c0045t0001 | 0/0 | 13097 | 2 | 1 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0020t0001 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0027t0001 | 0/0 | 13097 | 4 | 4 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0070t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0009c0092t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010c0010t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010c0010t0002 | 0/0 | 13097 | 9 | 3 | 4 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0010c0084t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0011c0009t0002 | 0/0 | 13097 | 10 | 2 | 4 | 1 | 1 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0012c0015t0001 | 0/0 | 13097 | 6 | 3 | 0 | 2 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0012c0099t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0013c0014t0001 | 0/0 | 13097 | 6 | 0 | 1 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0014c0018t0002 | 0/0 | 13097 | 5 | 0 | 3 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0014c0081t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0015c0016t0002 | 0/0 | 13097 | 5 | 0 | 0 | 5 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0015c0016t0006 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0016c0017t0003 | 0/0 | 13097 | 5 | 1 | 3 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0017c0022t0002 | 0/0 | 12764 | 5 | 5 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0018c0021t0002 | 0/0 | 13097 | 5 | 1 | 4 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0019c0028t0002 | 0/0 | 13097 | 4 | 0 | 3 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0020c0025t0001 | 0/0 | 13097 | 4 | 1 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0021c0026t0002 | 0/0 | 13097 | 4 | 0 | 0 | 0 | 0 | 4 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0022c0029t0001 | 0/0 | 13097 | 3 | 0 | 0 | 1 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0022c0059t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0023c0036t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0023c0053t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0024c0032t0001 | 0/0 | 13097 | 3 | 0 | 2 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0025c0037t0001 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0025c0069t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0026c0033t0002 | 0/0 | 13097 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0027c0052t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0027c0125t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0028c0035t0001 | 0/0 | 13097 | 3 | 3 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0029c0030t0001 | 0/0 | 13097 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0030c0031t0001 | 0/0 | 13097 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0031c0051t0001 | 0/0 | 13097 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0032c0050t0002 | 0/0 | 13097 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0033c0043t0002 | 0/0 | 13097 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0034c0039t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0035c0040t0002 | 0/0 | 13097 | 2 | 1 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0036c0038t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0037c0041t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0038c0044t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0039c0046t0001 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 0 | 2 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0040c0047t0002 | 0/0 | 13097 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0041c0049t0002 | 0/0 | 13097 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0042c0054t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0043c0055t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0044c0061t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0045c0063t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0046c0126t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0047c0065t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0048c0066t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0049c0068t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0050c0067t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0051c0120t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0052c0121t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0053c0119t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0054c0122t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0055c0123t0004 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0056c0118t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0057c0071t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0058c0073t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0059c0074t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0060c0117t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0061c0077t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0062c0076t0002 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0063c0098t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0064c0079t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0065c0093t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0066c0091t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0067c0082t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0068c0095t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0069c0083t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0070c0090t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0071c0089t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0072c0086t0001 | 0/0 | 13112 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0073c0087t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0074c0088t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0075c0085t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0076c0080t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0077c0078t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0078c0075t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0079c0100t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0080c0101t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0081c0102t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0082c0112t0002 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0083c0108t0002 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0084c0107t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0085c0106t0002 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0086c0111t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0087c0105t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0088c0104t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0089c0103t0001 | 0/0 | 13097 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0090c0115t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0091c0114t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0092c0072t0007 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0093c0116t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0094c0124t0002 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0095c0064t0001 | 0/0 | 13097 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0096c0057t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0097c0058t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0098c0056t0001 | 0/0 | 13097 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
a0099c0060t0001 | 0/0 | 13097 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | copy fasta | chr6 | 32036153 | 32114338 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0007t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0034t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0109t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0001c0110t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0012t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0019t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0042t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0042t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0094t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0096t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0002c0097t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0003t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0048t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0048t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0003c0113t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0008t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0011t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0004c0062t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0013t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0023t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0005c0024t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0001 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0006c0004t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0007c0005t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0006t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0045t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0008c0045t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0020t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0027t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0027t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0027t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0027t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0070t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0009c0092t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0010t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0010c0084t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0011c0009t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0015t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0012c0099t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0013c0014t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0018t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0018t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0018t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0018t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0014c0081t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0015c0016t0006g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0017t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0017t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0017t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0017t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0016c0017t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0022t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0022t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0022t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0022t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0017c0022t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0018c0021t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0028t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0028t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0028t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0019c0028t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0025t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0020c0025t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0026t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0026t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0026t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0021c0026t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0029t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0029t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0029t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0022c0059t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0023c0036t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0023c0053t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0024c0032t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0024c0032t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0024c0032t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0025c0037t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0025c0069t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0026c0033t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0026c0033t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0026c0033t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0027c0052t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0027c0125t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0028c0035t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0028c0035t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0028c0035t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0030t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0030t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0029c0030t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0031t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0031t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0030c0031t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0031c0051t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0031c0051t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0032c0050t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0032c0050t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0033c0043t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0033c0043t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0034c0039t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0034c0039t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0035c0040t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0035c0040t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0036c0038t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0036c0038t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0037c0041t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0037c0041t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0038c0044t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0038c0044t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0039c0046t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0039c0046t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0040c0047t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0040c0047t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0041c0049t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0041c0049t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0042c0054t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0043c0055t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0044c0061t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0045c0063t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0046c0126t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0047c0065t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0048c0066t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0049c0068t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0050c0067t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0051c0120t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0052c0121t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0053c0119t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0054c0122t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0055c0123t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0056c0118t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0057c0071t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0058c0073t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0059c0074t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0060c0117t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0061c0077t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0062c0076t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0063c0098t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0064c0079t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0065c0093t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0066c0091t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0067c0082t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0068c0095t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0069c0083t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0070c0090t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0071c0089t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0072c0086t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0073c0087t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0074c0088t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0075c0085t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0076c0080t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0077c0078t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0078c0075t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0079c0100t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0080c0101t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0081c0102t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0082c0112t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0083c0108t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0084c0107t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0085c0106t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0086c0111t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0087c0105t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0088c0104t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0089c0103t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0090c0115t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0091c0114t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0092c0072t0007g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0093c0116t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0094c0124t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0095c0064t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0096c0057t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0097c0058t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0098c0056t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
a0099c0060t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0019 | c0028 | t0002 | g0084 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0271 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00140 | hp1 | a0008 | c0006 | t0001 | g0323 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00140 | hp2 | a0092 | c0072 | t0007 | g0381 | EUR | GBR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00280 | hp1 | a0046 | c0126 | t0002 | g0083 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00323 | hp1 | a0014 | c0081 | t0002 | g0079 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00323 | hp2 | a0057 | c0071 | t0002 | g0203 | EUR | FIN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00408 | hp1 | a0002 | c0012 | t0002 | g0038 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00408 | hp2 | a0015 | c0016 | t0002 | g0359 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00423 | hp1 | a0003 | c0003 | t0002 | g0353 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00423 | hp2 | a0009 | c0020 | t0001 | g0046 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00438 | hp1 | a0051 | c0120 | t0002 | g0240 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00438 | hp2 | a0003 | c0003 | t0002 | g0362 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00558 | hp1 | a0004 | c0011 | t0001 | g0183 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0365 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00597 | hp1 | a0002 | c0012 | t0002 | g0036 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00597 | hp2 | a0009 | c0020 | t0001 | g0072 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00609 | hp1 | a0001 | c0034 | t0001 | g0256 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00609 | hp2 | a0015 | c0016 | t0002 | g0358 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00639 | hp1 | a0001 | c0007 | t0001 | g0278 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00642 | hp1 | a0031 | c0051 | t0001 | g0025 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00642 | hp2 | a0011 | c0009 | t0002 | g0002 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00673 | hp1 | a0070 | c0090 | t0001 | g0136 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00673 | hp2 | a0071 | c0089 | t0001 | g0018 | EAS | CHS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00733 | hp1 | a0001 | c0007 | t0001 | g0281 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00733 | hp2 | a0011 | c0009 | t0002 | g0045 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00735 | hp1 | a0032 | c0050 | t0002 | g0022 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00735 | hp2 | a0002 | c0019 | t0002 | g0060 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00738 | hp1 | a0019 | c0028 | t0002 | g0047 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00738 | hp2 | a0016 | c0017 | t0003 | g0208 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00741 | hp1 | a0035 | c0040 | t0002 | g0089 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG00741 | hp2 | a0004 | c0008 | t0001 | g0193 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01069 | hp1 | a0019 | c0028 | t0002 | g0085 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01069 | hp2 | a0006 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01070 | hp1 | a0024 | c0032 | t0001 | g0180 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01070 | hp2 | a0019 | c0028 | t0002 | g0082 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01071 | hp1 | a0006 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01071 | hp2 | a0024 | c0032 | t0001 | g0191 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01074 | hp1 | a0010 | c0010 | t0002 | g0024 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01081 | hp1 | a0031 | c0051 | t0001 | g0026 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01099 | hp1 | a0006 | c0004 | t0001 | g0001 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01099 | hp2 | a0010 | c0010 | t0002 | g0028 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01109 | hp1 | a0010 | c0010 | t0002 | g0029 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01167 | hp1 | a0018 | c0021 | t0002 | g0253 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01167 | hp2 | a0006 | c0004 | t0001 | g0199 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01169 | hp1 | a0006 | c0004 | t0001 | g0197 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01169 | hp2 | a0001 | c0034 | t0001 | g0265 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01175 | hp2 | a0004 | c0008 | t0001 | g0187 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01192 | hp1 | a0018 | c0021 | t0002 | g0250 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01243 | hp1 | a0050 | c0067 | t0001 | g0212 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01243 | hp2 | a0016 | c0017 | t0003 | g0211 | AMR | PUR | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01255 | hp1 | a0002 | c0019 | t0002 | g0003 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01256 | hp1 | a0002 | c0019 | t0002 | g0003 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01256 | hp2 | a0014 | c0018 | t0002 | g0007 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01257 | hp1 | a0004 | c0011 | t0001 | g0182 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01257 | hp2 | a0011 | c0009 | t0002 | g0002 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01258 | hp1 | a0004 | c0011 | t0001 | g0184 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01258 | hp2 | a0014 | c0018 | t0002 | g0007 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01346 | hp2 | a0068 | c0095 | t0001 | g0289 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01358 | hp1 | a0062 | c0076 | t0002 | g0053 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01361 | hp1 | a0010 | c0010 | t0002 | g0027 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01361 | hp2 | a0043 | c0055 | t0002 | g0065 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01433 | hp1 | a0006 | c0004 | t0001 | g0316 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01433 | hp2 | a0089 | c0103 | t0001 | g0101 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01496 | hp2 | a0002 | c0019 | t0002 | g0059 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01515 | hp1 | a0008 | c0045 | t0001 | g0337 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01515 | hp2 | a0041 | c0049 | t0002 | g0247 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01516 | hp1 | a0010 | c0010 | t0002 | g0006 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01516 | hp2 | a0088 | c0104 | t0001 | g0306 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01517 | hp1 | a0010 | c0010 | t0002 | g0006 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01517 | hp2 | a0041 | c0049 | t0002 | g0248 | EUR | IBS | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01884 | hp1 | a0027 | c0052 | t0002 | g0013 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01884 | hp2 | a0008 | c0006 | t0001 | g0338 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01891 | hp1 | a0032 | c0050 | t0002 | g0021 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01891 | hp2 | a0093 | c0116 | t0001 | g0378 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01934 | hp1 | a0056 | c0118 | t0002 | g0015 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01934 | hp2 | a0001 | c0007 | t0001 | g0310 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01943 | hp1 | a0002 | c0012 | t0002 | g0064 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01952 | hp1 | a0005 | c0024 | t0001 | g0222 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01952 | hp2 | a0018 | c0021 | t0002 | g0254 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01975 | hp1 | a0026 | c0033 | t0002 | g0152 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01978 | hp1 | a0018 | c0021 | t0002 | g0252 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01993 | hp1 | a0014 | c0018 | t0002 | g0092 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01993 | hp2 | a0002 | c0019 | t0002 | g0003 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02004 | hp1 | a0026 | c0033 | t0002 | g0153 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02027 | hp1 | a0005 | c0013 | t0001 | g0040 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02027 | hp2 | a0002 | c0012 | t0002 | g0037 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02040 | hp1 | a0004 | c0011 | t0001 | g0178 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02040 | hp2 | a0003 | c0003 | t0002 | g0373 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02055 | hp1 | a0009 | c0070 | t0001 | g0074 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02055 | hp2 | a0011 | c0009 | t0002 | g0141 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02071 | hp1 | a0075 | c0085 | t0002 | g0155 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02071 | hp2 | a0086 | c0111 | t0001 | g0277 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02080 | hp1 | a0008 | c0006 | t0001 | g0324 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02080 | hp2 | a0011 | c0009 | t0002 | g0056 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02083 | hp1 | a0003 | c0113 | t0002 | g0369 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02083 | hp2 | a0042 | c0054 | t0002 | g0158 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02129 | hp1 | a0087 | c0105 | t0001 | g0202 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02129 | hp2 | a0020 | c0025 | t0001 | g0005 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02132 | hp1 | a0005 | c0023 | t0001 | g0236 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02132 | hp2 | a0009 | c0020 | t0001 | g0070 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02145 | hp1 | a0009 | c0027 | t0001 | g0075 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02145 | hp2 | a0002 | c0042 | t0002 | g0076 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02148 | hp1 | a0026 | c0033 | t0002 | g0154 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02148 | hp2 | a0011 | c0009 | t0002 | g0055 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02155 | hp2 | a0023 | c0036 | t0002 | g0011 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02165 | hp1 | a0003 | c0003 | t0002 | g0371 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02257 | hp1 | a0004 | c0008 | t0001 | g0186 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02257 | hp2 | a0016 | c0017 | t0003 | g0207 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02258 | hp1 | a0035 | c0040 | t0002 | g0081 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02258 | hp2 | a0004 | c0008 | t0001 | g0177 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02280 | hp1 | a0008 | c0006 | t0001 | g0318 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02280 | hp2 | a0017 | c0022 | t0002 | g0343 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02293 | hp1 | a0002 | c0012 | t0002 | g0062 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02293 | hp2 | a0013 | c0014 | t0001 | g0292 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02300 | hp1 | a0002 | c0012 | t0002 | g0063 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02451 | hp1 | a0064 | c0079 | t0001 | g0379 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02451 | hp2 | a0004 | c0008 | t0001 | g0033 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02523 | hp1 | a0003 | c0003 | t0002 | g0374 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02523 | hp2 | a0004 | c0011 | t0001 | g0179 | EAS | KHV | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02572 | hp1 | a0061 | c0077 | t0002 | g0044 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02572 | hp2 | a0004 | c0008 | t0001 | g0213 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02602 | hp1 | a0008 | c0006 | t0001 | g0325 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02615 | hp1 | a0017 | c0022 | t0002 | g0345 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02615 | hp2 | a0060 | c0117 | t0002 | g0149 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02622 | hp1 | a0012 | c0015 | t0001 | g0334 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02622 | hp2 | a0010 | c0010 | t0002 | g0314 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02630 | hp1 | a0079 | c0100 | t0001 | g0319 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02630 | hp2 | a0004 | c0008 | t0001 | g0188 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02683 | hp1 | a0078 | c0075 | t0002 | g0067 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02683 | hp2 | a0073 | c0087 | t0002 | g0030 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02698 | hp1 | a0097 | c0058 | t0001 | g0219 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02698 | hp2 | a0044 | c0061 | t0001 | g0181 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02717 | hp1 | a0010 | c0084 | t0002 | g0041 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02717 | hp2 | a0004 | c0062 | t0001 | g0176 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02735 | hp1 | a0038 | c0044 | t0001 | g0329 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02735 | hp2 | a0011 | c0009 | t0002 | g0054 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02738 | hp1 | a0024 | c0032 | t0001 | g0190 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02738 | hp2 | a0021 | c0026 | t0002 | g0218 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02809 | hp1 | a0006 | c0004 | t0001 | g0198 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02809 | hp2 | a0027 | c0052 | t0002 | g0013 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02818 | hp1 | a0009 | c0027 | t0001 | g0068 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02818 | hp2 | a0004 | c0008 | t0001 | g0189 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02886 | hp1 | a0006 | c0004 | t0001 | g0195 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02886 | hp2 | a0033 | c0043 | t0002 | g0137 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02895 | hp1 | a0006 | c0004 | t0001 | g0201 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02895 | hp2 | a0009 | c0027 | t0001 | g0069 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02922 | hp1 | a0006 | c0004 | t0001 | g0001 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02922 | hp2 | a0063 | c0098 | t0002 | g0023 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02965 | hp1 | a0006 | c0004 | t0001 | g0347 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02965 | hp2 | a0028 | c0035 | t0001 | g0139 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02970 | hp1 | a0002 | c0042 | t0002 | g0142 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02970 | hp2 | a0027 | c0125 | t0002 | g0377 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02976 | hp1 | a0008 | c0045 | t0001 | g0336 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02976 | hp2 | a0004 | c0011 | t0001 | g0162 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03017 | hp1 | a0023 | c0053 | t0002 | g0161 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03041 | hp1 | a0006 | c0004 | t0001 | g0185 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03041 | hp2 | a0004 | c0008 | t0001 | g0315 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03098 | hp1 | a0048 | c0066 | t0002 | g0175 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03098 | hp2 | a0033 | c0043 | t0002 | g0032 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03130 | hp1 | a0009 | c0092 | t0001 | g0043 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03130 | hp2 | a0017 | c0022 | t0002 | g0344 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03139 | hp1 | a0010 | c0010 | t0002 | g0020 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03139 | hp2 | a0006 | c0004 | t0001 | g0001 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03195 | hp1 | a0025 | c0069 | t0001 | g0173 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03195 | hp2 | a0017 | c0022 | t0002 | g0341 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03209 | hp1 | a0004 | c0011 | t0001 | g0192 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03209 | hp2 | a0012 | c0099 | t0001 | g0333 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03239 | hp1 | a0012 | c0015 | t0001 | g0330 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03453 | hp1 | a0076 | c0080 | t0001 | g0380 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03453 | hp2 | a0011 | c0009 | t0002 | g0057 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03486 | hp1 | a0028 | c0035 | t0001 | g0051 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03486 | hp2 | a0025 | c0037 | t0001 | g0012 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03491 | hp1 | a0021 | c0026 | t0002 | g0217 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03491 | hp2 | a0039 | c0046 | t0001 | g0270 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03492 | hp1 | a0037 | c0041 | t0001 | g0035 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03492 | hp2 | a0021 | c0026 | t0002 | g0216 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03516 | hp1 | a0004 | c0008 | t0001 | g0138 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03516 | hp2 | a0008 | c0006 | t0001 | g0320 | AFR | ESN | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03540 | hp1 | a0006 | c0004 | t0001 | g0196 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03540 | hp2 | a0002 | c0096 | t0001 | g0134 | AFR | GWD | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03579 | hp1 | a0091 | c0114 | t0001 | g0140 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03579 | hp2 | a0055 | c0123 | t0004 | g0227 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03654 | hp1 | a0021 | c0026 | t0002 | g0215 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03654 | hp2 | a0001 | c0109 | t0001 | g0246 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03704 | hp1 | a0008 | c0006 | t0001 | g0322 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03704 | hp2 | a0069 | c0083 | t0002 | g0080 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03710 | hp1 | a0039 | c0046 | t0001 | g0263 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03710 | hp2 | a0096 | c0057 | t0001 | g0172 | SAS | PJL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03831 | hp1 | a0037 | c0041 | t0001 | g0146 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03831 | hp2 | a0098 | c0056 | t0001 | g0214 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03834 | hp1 | a0047 | c0065 | t0001 | g0346 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03834 | hp2 | a0084 | c0107 | t0002 | g0283 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03927 | hp1 | a0008 | c0006 | t0001 | g0317 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03927 | hp2 | a0022 | c0029 | t0001 | g0164 | SAS | BEB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04115 | hp1 | a0004 | c0011 | t0001 | g0194 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04115 | hp2 | a0008 | c0006 | t0001 | g0321 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04199 | hp1 | a0085 | c0106 | t0002 | g0275 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04199 | hp2 | a0011 | c0009 | t0002 | g0052 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04204 | hp2 | a0038 | c0044 | t0001 | g0328 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG04228 | hp2 | a0022 | c0029 | t0001 | g0157 | SAS | STU | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18522 | hp1 | a0025 | c0037 | t0001 | g0012 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18522 | hp2 | a0008 | c0006 | t0001 | g0339 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18612 | hp1 | a0008 | c0006 | t0001 | g0220 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0251 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18747 | hp2 | a0081 | c0102 | t0001 | g0103 | EAS | CHB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18906 | hp1 | a0045 | c0063 | t0001 | g0034 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18906 | hp2 | a0017 | c0022 | t0002 | g0342 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18939 | hp1 | a0030 | c0031 | t0001 | g0166 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18940 | hp2 | a0040 | c0047 | t0002 | g0361 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18941 | hp1 | a0022 | c0059 | t0001 | g0165 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18943 | hp1 | a0083 | c0108 | t0002 | g0372 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0350 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18945 | hp1 | a0005 | c0024 | t0001 | g0255 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18945 | hp2 | a0007 | c0005 | t0002 | g0004 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18948 | hp1 | a0012 | c0015 | t0001 | g0326 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18948 | hp2 | a0001 | c0007 | t0001 | g0280 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18949 | hp1 | a0001 | c0007 | t0001 | g0290 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18949 | hp2 | a0082 | c0112 | t0002 | g0349 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18950 | hp1 | a0001 | c0007 | t0001 | g0285 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18951 | hp1 | a0005 | c0013 | t0001 | g0235 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18951 | hp2 | a0009 | c0020 | t0001 | g0071 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18954 | hp2 | a0023 | c0036 | t0002 | g0011 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18956 | hp1 | a0013 | c0014 | t0001 | g0301 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18956 | hp2 | a0002 | c0094 | t0001 | g0129 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18961 | hp1 | a0005 | c0023 | t0001 | g0231 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18962 | hp1 | a0001 | c0007 | t0001 | g0288 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18963 | hp1 | a0013 | c0014 | t0001 | g0302 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18963 | hp2 | a0007 | c0005 | t0002 | g0094 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18967 | hp1 | a0013 | c0014 | t0001 | g0303 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18967 | hp2 | a0003 | c0048 | t0002 | g0360 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18970 | hp1 | a0013 | c0014 | t0001 | g0293 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18970 | hp2 | a0036 | c0038 | t0002 | g0090 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18972 | hp1 | a0015 | c0016 | t0002 | g0357 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18972 | hp2 | a0005 | c0013 | t0001 | g0241 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18973 | hp1 | a0003 | c0003 | t0002 | g0367 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18975 | hp1 | a0001 | c0007 | t0001 | g0286 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18977 | hp1 | a0029 | c0030 | t0001 | g0170 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18977 | hp2 | a0005 | c0013 | t0001 | g0230 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18980 | hp2 | a0002 | c0097 | t0002 | g0039 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18982 | hp1 | a0003 | c0003 | t0002 | g0048 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18984 | hp1 | a0007 | c0005 | t0002 | g0147 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18985 | hp1 | a0034 | c0039 | t0002 | g0078 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18985 | hp2 | a0005 | c0023 | t0001 | g0232 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18989 | hp1 | a0002 | c0012 | t0002 | g0077 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18990 | hp1 | a0015 | c0016 | t0002 | g0355 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18990 | hp2 | a0007 | c0005 | t0002 | g0042 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18993 | hp1 | a0005 | c0024 | t0001 | g0225 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18995 | hp2 | a0007 | c0005 | t0002 | g0096 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18998 | hp1 | a0003 | c0003 | t0002 | g0313 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18998 | hp2 | a0072 | c0086 | t0001 | g0122 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18999 | hp1 | a0040 | c0047 | t0002 | g0366 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18999 | hp2 | a0013 | c0014 | t0001 | g0312 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19000 | hp1 | a0005 | c0013 | t0001 | g0234 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19000 | hp2 | a0001 | c0007 | t0001 | g0279 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19002 | hp1 | a0004 | c0011 | t0001 | g0200 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19002 | hp2 | a0007 | c0005 | t0002 | g0098 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19004 | hp1 | a0029 | c0030 | t0001 | g0169 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0244 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19005 | hp2 | a0020 | c0025 | t0001 | g0005 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19007 | hp1 | a0009 | c0020 | t0001 | g0073 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19007 | hp2 | a0003 | c0003 | t0002 | g0354 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19009 | hp1 | a0015 | c0016 | t0006 | g0376 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19011 | hp1 | a0003 | c0003 | t0002 | g0351 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19011 | hp2 | a0001 | c0007 | t0001 | g0287 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19030 | hp1 | a0010 | c0010 | t0002 | g0019 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19030 | hp2 | a0094 | c0124 | t0002 | g0066 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19054 | hp1 | a0030 | c0031 | t0001 | g0206 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19054 | hp2 | a0007 | c0005 | t0002 | g0058 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19055 | hp1 | a0001 | c0007 | t0001 | g0284 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19055 | hp2 | a0029 | c0030 | t0001 | g0168 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19056 | hp2 | a0022 | c0029 | t0001 | g0167 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19057 | hp1 | a0005 | c0013 | t0001 | g0239 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0352 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19058 | hp1 | a0005 | c0023 | t0001 | g0237 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19060 | hp1 | a0034 | c0039 | t0002 | g0086 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19060 | hp2 | a0058 | c0073 | t0001 | g0296 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19062 | hp2 | a0007 | c0005 | t0002 | g0004 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19064 | hp1 | a0036 | c0038 | t0002 | g0091 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0375 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19065 | hp1 | a0005 | c0024 | t0001 | g0223 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19066 | hp1 | a0012 | c0015 | t0001 | g0332 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19067 | hp1 | a0005 | c0023 | t0001 | g0238 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19068 | hp2 | a0014 | c0018 | t0002 | g0087 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19070 | hp1 | a0003 | c0003 | t0002 | g0368 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19074 | hp1 | a0014 | c0018 | t0002 | g0088 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19078 | hp1 | a0015 | c0016 | t0002 | g0356 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19078 | hp2 | a0066 | c0091 | t0002 | g0143 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19079 | hp1 | a0005 | c0024 | t0001 | g0221 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19079 | hp2 | a0007 | c0005 | t0002 | g0097 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0364 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19080 | hp2 | a0020 | c0025 | t0001 | g0005 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19081 | hp1 | a0030 | c0031 | t0001 | g0171 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19081 | hp2 | a0059 | c0074 | t0001 | g0116 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0363 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19082 | hp2 | a0001 | c0110 | t0001 | g0274 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19083 | hp2 | a0007 | c0005 | t0002 | g0099 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19085 | hp1 | a0007 | c0005 | t0002 | g0093 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19086 | hp2 | a0003 | c0048 | t0005 | g0370 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19087 | hp1 | a0007 | c0005 | t0002 | g0095 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19089 | hp1 | a0007 | c0005 | t0002 | g0348 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19089 | hp2 | a0005 | c0013 | t0001 | g0233 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19090 | hp1 | a0002 | c0012 | t0002 | g0061 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19240 | hp1 | a0012 | c0015 | t0001 | g0327 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA19240 | hp2 | a0009 | c0027 | t0001 | g0050 | AFR | YRI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20129 | hp1 | a0049 | c0068 | t0002 | g0205 | AFR | ASW | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20129 | hp2 | a0052 | c0121 | t0001 | g0224 | AFR | ASW | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20752 | hp1 | a0080 | c0101 | t0001 | g0331 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20752 | hp2 | a0065 | c0093 | t0001 | g0144 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20805 | hp1 | a0001 | c0007 | t0001 | g0282 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20805 | hp2 | a0011 | c0009 | t0002 | g0002 | EUR | TSI | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | GIH | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20905 | hp2 | a0016 | c0017 | t0003 | g0210 | SAS | GIH | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01123 | hp1 | a0016 | c0017 | t0003 | g0209 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02109 | hp1 | a0010 | c0010 | t0001 | g0017 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02109 | hp2 | a0054 | c0122 | t0004 | g0228 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02486 | hp1 | a0028 | c0035 | t0001 | g0016 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02486 | hp2 | a0008 | c0006 | t0001 | g0340 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02559 | hp1 | a0077 | c0078 | t0001 | g0132 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG02559 | hp2 | a0001 | c0034 | t0001 | g0264 | AFR | ACB | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03471 | hp1 | a0090 | c0115 | t0001 | g0049 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG03471 | hp2 | a0020 | c0025 | t0001 | g0174 | AFR | MSL | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG06807 | hp1 | a0012 | c0015 | t0001 | g0335 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
HG06807 | hp2 | a0067 | c0082 | t0002 | g0014 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18955 | hp1 | a0074 | c0088 | t0001 | g0131 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA18955 | hp2 | a0099 | c0060 | t0001 | g0163 | EAS | JPT | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20300 | hp1 | a0018 | c0021 | t0002 | g0308 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA20300 | hp2 | a0053 | c0119 | t0004 | g0229 | AFR | USA | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA21309 | hp1 | a0007 | c0005 | t0002 | g0004 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
NA21309 | hp2 | a0095 | c0064 | t0001 | g0148 | AFR | LWK | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | TNXB_chr6_32036153_32114338 | TNXB | chr6 | 32036153 | 32114338 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041874
|
C | T | 1 | a0041 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.12530G>A | p.Ser4177Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12696/13097 | 12530/12735 | 4177/4244 | chr6 | 32041874 | ||
chr6:32041884
|
C | T | 1 | a0041 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.12520G>A | p.Asp4174Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12686/13097 | 12520/12735 | 4174/4244 | chr6 | 32041884 | ||
chr6:32041892
|
C | T | 1 | a0027 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.12512G>A | p.Arg4171His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12678/13097 | 12512/12735 | 4171/4244 | chr6 | 32041892 | ||
chr6:32042495
|
T | A | 12 | a0001a0013a0039others(9): Show | 81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
missense_variant | MODERATE | c.12170A>T | p.Asn4057Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12336/13097 | 12170/12735 | 4057/4244 | chr6 | 32042495 | ||
chr6:32042522
|
A | T | 1 | a0079 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.12143T>A | p.Leu4048His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12309/13097 | 12143/12735 | 4048/4244 | chr6 | 32042522 | ||
chr6:32042746
|
A | G | 10 | a0008a0012a0017others(7): Show | 36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
missense_variant | MODERATE | c.12011T>C | p.Met4004Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/44 | 12177/13097 | 12011/12735 | 4004/4244 | chr6 | 32042746 | ||
chr6:32042955
|
T | G | 27 | a0001a0008a0012others(24): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
missense_variant | MODERATE | c.11921A>C | p.Asn3974Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/44 | 12087/13097 | 11921/12735 | 3974/4244 | chr6 | 32042955 | ||
chr6:32043073
|
C | T | 2 | a0025a0050 | 4 | HG01243.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.11803G>A | p.Ala3935Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/44 | 11969/13097 | 11803/12735 | 3935/4244 | chr6 | 32043073 | ||
chr6:32043458
|
C | T | 40 | a0001a0004a0005others(37): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
missense_variant | MODERATE | c.11629G>A | p.Val3877Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11795/13097 | 11629/12735 | 3877/4244 | chr6 | 32043458 | ||
chr6:32043539
|
G | T | 16 | a0005a0007a0016others(13): Show | 59 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(56): Show |
missense_variant | MODERATE | c.11548C>A | p.Gln3850Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11714/13097 | 11548/12735 | 3850/4244 | chr6 | 32043539 | ||
chr6:32043718
|
ACCTCTTG others(113): Show |
A | 1 | a0083 | 1 | NA18943.hp1 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.11441_11530+30del | p.Gly3814_Thr3843del | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11441/12735 | 3814/4244 | chr6 | 32043718 | |||
chr6:32043862
|
T | C | 2 | a0069a0091 | 2 | HG03579.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.11417A>G | p.Gln3806Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11583/13097 | 11417/12735 | 3806/4244 | chr6 | 32043862 | ||
chr6:32044483
|
G | A | 2 | a0014a0034 | 8 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.11161C>T | p.Arg3721Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11327/13097 | 11161/12735 | 3721/4244 | chr6 | 32044483 | ||
chr6:32044684
|
A | C | 8 | a0003a0015a0018others(5): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
missense_variant | MODERATE | c.10960T>G | p.Ser3654Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11126/13097 | 10960/12735 | 3654/4244 | chr6 | 32044684 | ||
chr6:32045029
|
G | T | 1 | a0051 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.10904C>A | p.Pro3635His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 11070/13097 | 10904/12735 | 3635/4244 | chr6 | 32045029 | ||
chr6:32045120
|
C | T | 2 | a0054a0055 | 2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.10813G>A | p.Asp3605Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 10979/13097 | 10813/12735 | 3605/4244 | chr6 | 32045120 | ||
chr6:32046196
|
C | T | 1 | a0045 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.10585G>A | p.Val3529Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10751/13097 | 10585/12735 | 3529/4244 | chr6 | 32046196 | ||
chr6:32046198
|
G | A | 1 | a0027 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.10583C>T | p.Pro3528Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10749/13097 | 10583/12735 | 3528/4244 | chr6 | 32046198 | ||
chr6:32046292
|
C | T | 1 | a0085 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.10489G>A | p.Ala3497Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10655/13097 | 10489/12735 | 3497/4244 | chr6 | 32046292 | ||
chr6:32046421
|
C | T | 1 | a0074 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.10360G>A | p.Glu3454Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10526/13097 | 10360/12735 | 3454/4244 | chr6 | 32046421 | ||
chr6:32047988
|
C | T | 1 | a0044 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.10070G>A | p.Arg3357His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/44 | 10236/13097 | 10070/12735 | 3357/4244 | chr6 | 32047988 | ||
chr6:32047998
|
G | A | 1 | a0018 | 5 | HG01167.hp1 HG01192.hp1 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.10060C>T | p.Pro3354Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/44 | 10226/13097 | 10060/12735 | 3354/4244 | chr6 | 32047998 | ||
chr6:32048363
|
C | G | 1 | a0086 | 1 | HG02071.hp2 | missense_variant&splice_region_variant | MODERATE | c.10045G>C | p.Ala3349Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 10211/13097 | 10045/12735 | 3349/4244 | chr6 | 32048363 | ||
chr6:32049366
|
C | T | 1 | a0097 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.9661G>A | p.Val3221Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9827/13097 | 9661/12735 | 3221/4244 | chr6 | 32049366 | ||
chr6:32049384
|
C | T | 3 | a0005a0051a0052 | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.9643G>A | p.Glu3215Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9809/13097 | 9643/12735 | 3215/4244 | chr6 | 32049384 | ||
chr6:32049386
|
C | A | 1 | a0011 | 10 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(7): Show |
missense_variant | MODERATE | c.9641G>T | p.Gly3214Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9807/13097 | 9641/12735 | 3214/4244 | chr6 | 32049386 | ||
chr6:32049396
|
G | C | 2 | a0065a0092 | 2 | HG00140.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.9631C>G | p.Arg3211Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9797/13097 | 9631/12735 | 3211/4244 | chr6 | 32049396 | ||
chr6:32049456
|
C | T | 2 | a0025a0050 | 4 | HG01243.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.9571G>A | p.Gly3191Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9737/13097 | 9571/12735 | 3191/4244 | chr6 | 32049456 | ||
chr6:32049465
|
C | T | 3 | a0008a0025a0050 | 18 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(15): Show |
missense_variant | MODERATE | c.9562G>A | p.Val3188Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9728/13097 | 9562/12735 | 3188/4244 | chr6 | 32049465 | ||
chr6:32049501
|
C | T | 1 | a0087 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.9526G>A | p.Gly3176Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9692/13097 | 9526/12735 | 3176/4244 | chr6 | 32049501 | ||
chr6:32050249
|
A | C | 1 | a0088 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.9188T>G | p.Leu3063Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/44 | 9354/13097 | 9188/12735 | 3063/4244 | chr6 | 32050249 | ||
chr6:32052700
|
C | T | 1 | a0044 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.9085G>A | p.Val3029Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9251/13097 | 9085/12735 | 3029/4244 | chr6 | 32052700 | ||
chr6:32052745
|
A | G | 1 | a0038 | 2 | HG02735.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.9040T>C | p.Cys3014Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9206/13097 | 9040/12735 | 3014/4244 | chr6 | 32052745 | ||
chr6:32053418
|
C | T | 1 | a0040 | 2 | NA18940.hp2 NA18999.hp1 |
missense_variant | MODERATE | c.8761G>A | p.Val2921Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8927/13097 | 8761/12735 | 2921/4244 | chr6 | 32053418 | ||
chr6:32053499
|
C | T | 2 | a0026a0056 | 4 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
missense_variant | MODERATE | c.8680G>A | p.Glu2894Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8846/13097 | 8680/12735 | 2894/4244 | chr6 | 32053499 | ||
chr6:32053585
|
A | G | 3 | a0005a0051a0052 | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.8594T>C | p.Met2865Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8760/13097 | 8594/12735 | 2865/4244 | chr6 | 32053585 | ||
chr6:32055974
|
C | CACGCATC others(8): Show |
1 | a0072 | 1 | NA18998.hp2 | conservative_inframe_insertion | MODERATE | c.8329_8343dupCCCCAG others(9): Show |
p.Arg2781_Val2782ins others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8509/13097 | 8343/12735 | 2781/4244 | chr6 | 32055974 | ||
chr6:32056108
|
G | A | 1 | a0090 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.8210C>T | p.Pro2737Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8376/13097 | 8210/12735 | 2737/4244 | chr6 | 32056108 | ||
chr6:32056126
|
G | C | 5 | a0010a0031a0032others(2): Show | 17 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(14): Show |
missense_variant | MODERATE | c.8192C>G | p.Pro2731Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8358/13097 | 8192/12735 | 2731/4244 | chr6 | 32056126 | ||
chr6:32056592
|
C | A | 1 | a0061 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.8137G>T | p.Val2713Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8303/13097 | 8137/12735 | 2713/4244 | chr6 | 32056592 | ||
chr6:32056616
|
C | T | 1 | a0034 | 2 | NA18985.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.8113G>A | p.Val2705Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8279/13097 | 8113/12735 | 2705/4244 | chr6 | 32056616 | ||
chr6:32056618
|
C | T | 10 | a0009a0028a0064others(7): Show | 22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
missense_variant | MODERATE | c.8111G>A | p.Arg2704His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8277/13097 | 8111/12735 | 2704/4244 | chr6 | 32056618 | ||
chr6:32056775
|
C | T | 1 | a0075 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.7954G>A | p.Glu2652Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8120/13097 | 7954/12735 | 2652/4244 | chr6 | 32056775 | ||
chr6:32056783
|
G | A | 2 | a0071a0082 | 2 | HG00673.hp2 NA18949.hp2 |
missense_variant | MODERATE | c.7946C>T | p.Thr2649Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8112/13097 | 7946/12735 | 2649/4244 | chr6 | 32056783 | ||
chr6:32058081
|
G | A | 1 | a0070 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.7802C>T | p.Pro2601Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7968/13097 | 7802/12735 | 2601/4244 | chr6 | 32058081 | ||
chr6:32058093
|
C | T | 20 | a0004a0005a0006others(17): Show | 87 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(84): Show |
missense_variant | MODERATE | c.7790G>A | p.Arg2597Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7956/13097 | 7790/12735 | 2597/4244 | chr6 | 32058093 | ||
chr6:32058155
|
AGTGACCT others(3332): Show |
A | 1 | a0017 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
conservative_inframe_deletion | MODERATE | c.7395_7727del | p.Thr2465_Val2575del | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7893/13097 | 7395/12735 | 2465/4244 | chr6 | 32058155 | ||
chr6:32058250
|
G | A | 1 | a0046 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.7633C>T | p.Pro2545Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7799/13097 | 7633/12735 | 2545/4244 | chr6 | 32058250 | ||
chr6:32058330
|
C | T | 64 | a0001a0003a0004others(61): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
missense_variant | MODERATE | c.7553G>A | p.Gly2518Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7719/13097 | 7553/12735 | 2518/4244 | chr6 | 32058330 | ||
chr6:32061406
|
C | T | 15 | a0004a0006a0016others(12): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
missense_variant | MODERATE | c.7483G>A | p.Gly2495Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7649/13097 | 7483/12735 | 2495/4244 | chr6 | 32061406 | ||
chr6:32061472
|
G | A | 1 | a0096 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.7417C>T | p.Arg2473Cys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7583/13097 | 7417/12735 | 2473/4244 | chr6 | 32061472 | ||
chr6:32061528
|
A | G | 1 | a0017 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.7361T>C | p.Val2454Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7527/13097 | 7361/12735 | 2454/4244 | chr6 | 32061528 | ||
chr6:32061537
|
C | T | 1 | a0039 | 2 | HG03491.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.7352G>A | p.Arg2451Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7518/13097 | 7352/12735 | 2451/4244 | chr6 | 32061537 | ||
chr6:32061541
|
C | T | 1 | a0098 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.7348G>A | p.Gly2450Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7514/13097 | 7348/12735 | 2450/4244 | chr6 | 32061541 | ||
chr6:32061542
|
G | C | 1 | a0042 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.7347C>G | p.Asp2449Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7513/13097 | 7347/12735 | 2449/4244 | chr6 | 32061542 | ||
chr6:32061592
|
C | T | 1 | a0027 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.7297G>A | p.Val2433Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7463/13097 | 7297/12735 | 2433/4244 | chr6 | 32061592 | ||
chr6:32061654
|
G | A | 10 | a0009a0028a0064others(7): Show | 22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
missense_variant | MODERATE | c.7235C>T | p.Pro2412Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7401/13097 | 7235/12735 | 2412/4244 | chr6 | 32061654 | ||
chr6:32062274
|
C | T | 1 | a0076 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.7051G>A | p.Gly2351Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7217/13097 | 7051/12735 | 2351/4244 | chr6 | 32062274 | ||
chr6:32062354
|
G | T | 2 | a0064a0093 | 2 | HG01891.hp2 HG02451.hp1 |
missense_variant | MODERATE | c.6971C>A | p.Thr2324Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7137/13097 | 6971/12735 | 2324/4244 | chr6 | 32062354 | ||
chr6:32062423
|
G | T | 3 | a0005a0051a0052 | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.6902C>A | p.Pro2301His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7068/13097 | 6902/12735 | 2301/4244 | chr6 | 32062423 | ||
chr6:32064851
|
C | G | 1 | a0007 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
missense_variant | MODERATE | c.6811G>C | p.Val2271Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6977/13097 | 6811/12735 | 2271/4244 | chr6 | 32064851 | ||
chr6:32064968
|
C | T | 1 | a0036 | 2 | NA18970.hp2 NA19064.hp1 |
missense_variant | MODERATE | c.6694G>A | p.Asp2232Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6860/13097 | 6694/12735 | 2232/4244 | chr6 | 32064968 | ||
chr6:32064979
|
A | T | 6 | a0005a0051a0052others(3): Show | 22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
missense_variant | MODERATE | c.6683T>A | p.Phe2228Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6849/13097 | 6683/12735 | 2228/4244 | chr6 | 32064979 | ||
chr6:32065054
|
C | T | 1 | a0015 | 6 | HG00408.hp2 HG00609.hp2 NA18972.hp1 others(3): Show |
missense_variant | MODERATE | c.6608G>A | p.Arg2203Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6774/13097 | 6608/12735 | 2203/4244 | chr6 | 32065054 | ||
chr6:32067697
|
G | A | 1 | a0052 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.6508C>T | p.Arg2170Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6674/13097 | 6508/12735 | 2170/4244 | chr6 | 32067697 | ||
chr6:32067777
|
C | T | 1 | a0054 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.6428G>A | p.Gly2143Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6594/13097 | 6428/12735 | 2143/4244 | chr6 | 32067777 | ||
chr6:32067826
|
C | T | 18 | a0004a0006a0016others(15): Show | 71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
missense_variant | MODERATE | c.6379G>A | p.Val2127Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6545/13097 | 6379/12735 | 2127/4244 | chr6 | 32067826 | ||
chr6:32068672
|
C | T | 2 | a0050a0077 | 2 | HG01243.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.5938G>A | p.Ala1980Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6104/13097 | 5938/12735 | 1980/4244 | chr6 | 32068672 | ||
chr6:32068945
|
T | C | 1 | a0099 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.5779A>G | p.Ile1927Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5945/13097 | 5779/12735 | 1927/4244 | chr6 | 32068945 | ||
chr6:32068978
|
T | C | 1 | a0033 | 2 | HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.5746A>G | p.Thr1916Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5912/13097 | 5746/12735 | 1916/4244 | chr6 | 32068978 | ||
chr6:32069011
|
C | T | 1 | a0006 | 14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
missense_variant | MODERATE | c.5713G>A | p.Glu1905Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5879/13097 | 5713/12735 | 1905/4244 | chr6 | 32069011 | ||
chr6:32069592
|
C | T | 1 | a0027 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.5548G>A | p.Gly1850Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5714/13097 | 5548/12735 | 1850/4244 | chr6 | 32069592 | ||
chr6:32069698
|
G | C | 1 | a0030 | 3 | NA18939.hp1 NA19054.hp1 NA19081.hp1 |
missense_variant | MODERATE | c.5442C>G | p.Asp1814Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5608/13097 | 5442/12735 | 1814/4244 | chr6 | 32069698 | ||
chr6:32069724
|
A | G | 1 | a0089 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.5416T>C | p.Phe1806Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/44 | 5582/13097 | 5416/12735 | 1806/4244 | chr6 | 32069724 | ||
chr6:32070362
|
C | T | 1 | a0081 | 1 | NA18747.hp2 | stop_gained | HIGH | c.5043G>A | p.Trp1681* | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/44 | 5209/13097 | 5043/12735 | 1681/4244 | chr6 | 32070362 | ||
chr6:32072095
|
C | T | 3 | a0005a0051a0052 | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.4885G>A | p.Glu1629Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/44 | 5051/13097 | 4885/12735 | 1629/4244 | chr6 | 32072095 | ||
chr6:32072218
|
T | C | 1 | a0037 | 2 | HG03492.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.4762A>G | p.Ile1588Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/44 | 4928/13097 | 4762/12735 | 1588/4244 | chr6 | 32072218 | ||
chr6:32073766
|
G | A | 2 | a0061a0062 | 2 | HG01358.hp1 HG02572.hp1 |
missense_variant | MODERATE | c.4562C>T | p.Ala1521Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4728/13097 | 4562/12735 | 1521/4244 | chr6 | 32073766 | ||
chr6:32073844
|
G | A | 2 | a0031a0063 | 3 | HG00642.hp1 HG01081.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.4484C>T | p.Thr1495Ile | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4650/13097 | 4484/12735 | 1495/4244 | chr6 | 32073844 | ||
chr6:32073896
|
C | T | 1 | a0077 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4432G>A | p.Gly1478Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/44 | 4598/13097 | 4432/12735 | 1478/4244 | chr6 | 32073896 | ||
chr6:32079167
|
C | T | 6 | a0011a0023a0042others(3): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
missense_variant | MODERATE | c.4241G>A | p.Arg1414Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4407/13097 | 4241/12735 | 1414/4244 | chr6 | 32079167 | ||
chr6:32079291
|
G | T | 1 | a0078 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.4117C>A | p.Pro1373Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4283/13097 | 4117/12735 | 1373/4244 | chr6 | 32079291 | ||
chr6:32081646
|
C | G | 1 | a0059 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.3764G>C | p.Arg1255Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3930/13097 | 3764/12735 | 1255/4244 | chr6 | 32081646 | ||
chr6:32081646
|
C | T | 6 | a0008a0012a0038others(3): Show | 26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
missense_variant | MODERATE | c.3764G>A | p.Arg1255His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3930/13097 | 3764/12735 | 1255/4244 | chr6 | 32081646 | ||
chr6:32081652
|
G | T | 2 | a0054a0055 | 2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.3758C>A | p.Pro1253His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3924/13097 | 3758/12735 | 1253/4244 | chr6 | 32081652 | ||
chr6:32082290
|
T | C | 50 | a0001a0003a0004others(47): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): Show |
missense_variant | MODERATE | c.3482A>G | p.His1161Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/44 | 3648/13097 | 3482/12735 | 1161/4244 | chr6 | 32082290 | ||
chr6:32084449
|
T | C | 1 | a0058 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.3409A>G | p.Lys1137Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3575/13097 | 3409/12735 | 1137/4244 | chr6 | 32084449 | ||
chr6:32084478
|
T | C | 3 | a0028a0090a0091 | 5 | HG02486.hp1 HG02965.hp2 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.3380A>G | p.Lys1127Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3546/13097 | 3380/12735 | 1127/4244 | chr6 | 32084478 | ||
chr6:32084586
|
G | T | 3 | a0053a0054a0055 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.3272C>A | p.Ser1091Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3438/13097 | 3272/12735 | 1091/4244 | chr6 | 32084586 | ||
chr6:32084632
|
C | T | 1 | a0092 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.3226G>A | p.Asp1076Asn | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3392/13097 | 3226/12735 | 1076/4244 | chr6 | 32084632 | ||
chr6:32084667
|
C | T | 1 | a0057 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.3191G>A | p.Arg1064His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3357/13097 | 3191/12735 | 1064/4244 | chr6 | 32084667 | ||
chr6:32085951
|
C | T | 1 | a0095 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2947G>A | p.Ala983Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/44 | 3113/13097 | 2947/12735 | 983/4244 | chr6 | 32085951 | ||
chr6:32088803
|
A | C | 19 | a0004a0006a0016others(16): Show | 72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
missense_variant | MODERATE | c.2761T>G | p.Ser921Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/44 | 2927/13097 | 2761/12735 | 921/4244 | chr6 | 32088803 | ||
chr6:32088848
|
C | A | 1 | a0032 | 2 | HG00735.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.2716G>T | p.Val906Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/44 | 2882/13097 | 2716/12735 | 906/4244 | chr6 | 32088848 | ||
chr6:32089349
|
G | A | 1 | a0093 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2389C>T | p.Arg797Trp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2555/13097 | 2389/12735 | 797/4244 | chr6 | 32089349 | ||
chr6:32095878
|
G | A | 1 | a0056 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1975C>T | p.Arg659Cys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2141/13097 | 1975/12735 | 659/4244 | chr6 | 32095878 | ||
chr6:32095888
|
G | C | 2 | a0054a0055 | 2 | HG02109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1965C>G | p.Asp655Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2131/13097 | 1965/12735 | 655/4244 | chr6 | 32095888 | ||
chr6:32095904
|
C | T | 7 | a0004a0006a0020others(4): Show | 44 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(41): Show |
missense_variant | MODERATE | c.1949G>A | p.Arg650His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2115/13097 | 1949/12735 | 650/4244 | chr6 | 32095904 | ||
chr6:32095926
|
T | C | 1 | a0031 | 2 | HG00642.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.1927A>G | p.Thr643Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2093/13097 | 1927/12735 | 643/4244 | chr6 | 32095926 | ||
chr6:32096016
|
T | C | 6 | a0005a0051a0052others(3): Show | 22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
missense_variant | MODERATE | c.1837A>G | p.Ser613Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2003/13097 | 1837/12735 | 613/4244 | chr6 | 32096016 | ||
chr6:32096321
|
C | T | 18 | a0004a0006a0016others(15): Show | 69 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(66): Show |
missense_variant | MODERATE | c.1532G>A | p.Arg511His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1698/13097 | 1532/12735 | 511/4244 | chr6 | 32096321 | ||
chr6:32096384
|
C | T | 1 | a0013 | 6 | HG02293.hp2 NA18956.hp1 NA18963.hp1 others(3): Show |
missense_variant | MODERATE | c.1469G>A | p.Arg490Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1635/13097 | 1469/12735 | 490/4244 | chr6 | 32096384 | ||
chr6:32096594
|
A | G | 1 | a0047 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1259T>C | p.Val420Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1425/13097 | 1259/12735 | 420/4244 | chr6 | 32096594 | ||
chr6:32096752
|
G | C | 1 | a0094 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1101C>G | p.Asp367Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1267/13097 | 1101/12735 | 367/4244 | chr6 | 32096752 | ||
chr6:32096949
|
T | C | 2 | a0019a0046 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
missense_variant | MODERATE | c.904A>G | p.Thr302Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1070/13097 | 904/12735 | 302/4244 | chr6 | 32096949 | ||
chr6:32097234
|
C | T | 1 | a0095 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.619G>A | p.Gly207Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 785/13097 | 619/12735 | 207/4244 | chr6 | 32097234 | ||
chr6:32097246
|
C | T | 5 | a0004a0006a0024others(2): Show | 39 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(36): Show |
missense_variant | MODERATE | c.607G>A | p.Val203Met | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 773/13097 | 607/12735 | 203/4244 | chr6 | 32097246 | ||
chr6:32097336
|
C | T | 7 | a0022a0029a0030others(4): Show | 14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
missense_variant | MODERATE | c.517G>A | p.Ala173Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 683/13097 | 517/12735 | 173/4244 | chr6 | 32097336 | ||
chr6:32098086
|
C | T | 1 | a0043 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.113G>A | p.Arg38Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/44 | 279/13097 | 113/12735 | 38/4244 | chr6 | 32098086 | ||
chr6:32098113
|
C | T | 2 | a0023a0042 | 4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
missense_variant | MODERATE | c.86G>A | p.Arg29Gln | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/44 | 252/13097 | 86/12735 | 29/4244 | chr6 | 32098113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041421
|
G | A | 1 | a0001c0109 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.12663C>T | p.Phe4221Phe | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 12829/13097 | 12663/12735 | 4221/4244 | chr6 | 32041421 | ||
chr6:32041792
|
G | A | 1 | a0001c0110 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.12612C>T | p.Tyr4204Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/44 | 12778/13097 | 12612/12735 | 4204/4244 | chr6 | 32041792 | ||
chr6:32042103
|
G | A | 1 | a0007c0005 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
synonymous_variant | LOW | c.12378C>T | p.Asp4126Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 42/44 | 12544/13097 | 12378/12735 | 4126/4244 | chr6 | 32042103 | ||
chr6:32042509
|
G | C | 4 | a0005c0013a0005c0023a0005c0024others(1): Show | 18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
synonymous_variant | LOW | c.12156C>G | p.Arg4052Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/44 | 12322/13097 | 12156/12735 | 4052/4244 | chr6 | 32042509 | ||
chr6:32043471
|
C | T | 51 | a0001c0001a0001c0007a0001c0034others(48): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
synonymous_variant | LOW | c.11616G>A | p.Val3872Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11782/13097 | 11616/12735 | 3872/4244 | chr6 | 32043471 | ||
chr6:32043540
|
T | C | 19 | a0005c0013a0005c0023a0005c0024others(16): Show | 59 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(56): Show |
synonymous_variant | LOW | c.11547A>G | p.Thr3849Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/44 | 11713/13097 | 11547/12735 | 3849/4244 | chr6 | 32043540 | ||
chr6:32043867
|
A | G | 26 | a0004c0008a0004c0011a0004c0062others(23): Show | 85 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
synonymous_variant | LOW | c.11412T>C | p.Asp3804Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/44 | 11578/13097 | 11412/12735 | 3804/4244 | chr6 | 32043867 | ||
chr6:32044502
|
C | T | 6 | a0007c0005a0010c0010a0027c0125others(3): Show | 30 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(27): Show |
synonymous_variant | LOW | c.11142G>A | p.Thr3714Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11308/13097 | 11142/12735 | 3714/4244 | chr6 | 32044502 | ||
chr6:32044556
|
A | T | 16 | a0001c0001a0001c0007a0001c0109others(13): Show | 79 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(76): Show |
synonymous_variant | LOW | c.11088T>A | p.Thr3696Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/44 | 11254/13097 | 11088/12735 | 3696/4244 | chr6 | 32044556 | ||
chr6:32045040
|
C | T | 4 | a0001c0007a0068c0095a0084c0107others(1): Show | 15 | HG00639.hp1 HG00733.hp1 HG01346.hp2 others(12): Show |
synonymous_variant | LOW | c.10893G>A | p.Lys3631Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 11059/13097 | 10893/12735 | 3631/4244 | chr6 | 32045040 | ||
chr6:32045256
|
T | C | 2 | a0004c0062a0024c0032 | 4 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.10677A>G | p.Leu3559Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/44 | 10843/13097 | 10677/12735 | 3559/4244 | chr6 | 32045256 | ||
chr6:32046227
|
G | A | 1 | a0009c0092 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.10554C>T | p.Tyr3518Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10720/13097 | 10554/12735 | 3518/4244 | chr6 | 32046227 | ||
chr6:32046413
|
G | A | 3 | a0053c0119a0054c0122a0055c0123 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.10368C>T | p.Thr3456Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/44 | 10534/13097 | 10368/12735 | 3456/4244 | chr6 | 32046413 | ||
chr6:32048559
|
C | T | 1 | a0043c0055 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.9849G>A | p.Thr3283Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 10015/13097 | 9849/12735 | 3283/4244 | chr6 | 32048559 | ||
chr6:32048646
|
G | A | 1 | a0023c0036 | 2 | HG02155.hp2 NA18954.hp2 |
synonymous_variant | LOW | c.9762C>T | p.Pro3254Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/44 | 9928/13097 | 9762/12735 | 3254/4244 | chr6 | 32048646 | ||
chr6:32049328
|
A | G | 10 | a0002c0012a0002c0019a0002c0097others(7): Show | 23 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
synonymous_variant | LOW | c.9699T>C | p.His3233His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9865/13097 | 9699/12735 | 3233/4244 | chr6 | 32049328 | ||
chr6:32049355
|
C | T | 1 | a0008c0045 | 2 | HG01515.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.9672G>A | p.Leu3224Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9838/13097 | 9672/12735 | 3224/4244 | chr6 | 32049355 | ||
chr6:32049364
|
C | T | 1 | a0005c0023 | 5 | HG02132.hp1 NA18961.hp1 NA18985.hp2 others(2): Show |
synonymous_variant | LOW | c.9663G>A | p.Val3221Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/44 | 9829/13097 | 9663/12735 | 3221/4244 | chr6 | 32049364 | ||
chr6:32050269
|
C | T | 1 | a0060c0117 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.9168G>A | p.Glu3056Glu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/44 | 9334/13097 | 9168/12735 | 3056/4244 | chr6 | 32050269 | ||
chr6:32052785
|
G | A | 1 | a0042c0054 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.9000C>T | p.Gly3000Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/44 | 9166/13097 | 9000/12735 | 3000/4244 | chr6 | 32052785 | ||
chr6:32053581
|
G | A | 5 | a0005c0013a0005c0023a0005c0024others(2): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.8598C>T | p.Val2866Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/44 | 8764/13097 | 8598/12735 | 2866/4244 | chr6 | 32053581 | ||
chr6:32055855
|
C | A | 1 | a0086c0111 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.8463G>T | p.Val2821Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/44 | 8629/13097 | 8463/12735 | 2821/4244 | chr6 | 32055855 | ||
chr6:32056842
|
A | G | 1 | a0014c0081 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.7887T>C | p.Pro2629Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8053/13097 | 7887/12735 | 2629/4244 | chr6 | 32056842 | ||
chr6:32056863
|
G | A | 2 | a0005c0024a0052c0121 | 6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
synonymous_variant | LOW | c.7866C>T | p.Thr2622Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/44 | 8032/13097 | 7866/12735 | 2622/4244 | chr6 | 32056863 | ||
chr6:32058086
|
C | T | 9 | a0014c0018a0014c0081a0019c0028others(6): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
synonymous_variant | LOW | c.7797G>A | p.Leu2599Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7963/13097 | 7797/12735 | 2599/4244 | chr6 | 32058086 | ||
chr6:32058203
|
G | A | 12 | a0008c0006a0008c0045a0012c0015others(9): Show | 31 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(28): Show |
synonymous_variant | LOW | c.7680C>T | p.Asp2560Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/44 | 7846/13097 | 7680/12735 | 2560/4244 | chr6 | 32058203 | ||
chr6:32061428
|
G | A | 2 | a0019c0028a0046c0126 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
synonymous_variant | LOW | c.7461C>T | p.Arg2487Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7627/13097 | 7461/12735 | 2487/4244 | chr6 | 32061428 | ||
chr6:32061449
|
A | G | 73 | a0001c0001a0001c0007a0001c0034others(70): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
synonymous_variant | LOW | c.7440T>C | p.Tyr2480Tyr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7606/13097 | 7440/12735 | 2480/4244 | chr6 | 32061449 | ||
chr6:32061476
|
A | G | 1 | a0096c0057 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.7413T>C | p.Pro2471Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7579/13097 | 7413/12735 | 2471/4244 | chr6 | 32061476 | ||
chr6:32061512
|
G | A | 4 | a0009c0027a0028c0035a0090c0115others(1): Show | 9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
synonymous_variant | LOW | c.7377C>T | p.Gly2459Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7543/13097 | 7377/12735 | 2459/4244 | chr6 | 32061512 | ||
chr6:32061518
|
A | G | 1 | a0017c0022 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.7371T>C | p.Val2457Val | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7537/13097 | 7371/12735 | 2457/4244 | chr6 | 32061518 | ||
chr6:32061638
|
T | C | 65 | a0001c0001a0001c0007a0001c0034others(62): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(245): Show |
synonymous_variant | LOW | c.7251A>G | p.Leu2417Leu | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/44 | 7417/13097 | 7251/12735 | 2417/4244 | chr6 | 32061638 | ||
chr6:32062200
|
G | A | 1 | a0022c0059 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.7125C>T | p.His2375His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/44 | 7291/13097 | 7125/12735 | 2375/4244 | chr6 | 32062200 | ||
chr6:32064912
|
C | T | 3 | a0053c0119a0054c0122a0055c0123 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.6750G>A | p.Ser2250Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6916/13097 | 6750/12735 | 2250/4244 | chr6 | 32064912 | ||
chr6:32064966
|
G | A | 39 | a0001c0001a0001c0007a0001c0034others(36): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
synonymous_variant | LOW | c.6696C>T | p.Asp2232Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/44 | 6862/13097 | 6696/12735 | 2232/4244 | chr6 | 32064966 | ||
chr6:32067692
|
G | A | 5 | a0005c0013a0005c0023a0005c0024others(2): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.6513C>T | p.Arg2171Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6679/13097 | 6513/12735 | 2171/4244 | chr6 | 32067692 | ||
chr6:32067857
|
G | A | 9 | a0002c0096a0005c0013a0005c0023others(6): Show | 23 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(20): Show |
synonymous_variant | LOW | c.6348C>T | p.Thr2116Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6514/13097 | 6348/12735 | 2116/4244 | chr6 | 32067857 | ||
chr6:32067917
|
C | T | 2 | a0019c0028a0046c0126 | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
synonymous_variant | LOW | c.6288G>A | p.Pro2096Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6454/13097 | 6288/12735 | 2096/4244 | chr6 | 32067917 | ||
chr6:32067929
|
G | A | 1 | a0002c0097 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.6276C>T | p.Pro2092Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/44 | 6442/13097 | 6276/12735 | 2092/4244 | chr6 | 32067929 | ||
chr6:32068580
|
G | A | 22 | a0004c0008a0004c0011a0004c0062others(19): Show | 71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
synonymous_variant | LOW | c.6030C>T | p.Pro2010Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6196/13097 | 6030/12735 | 2010/4244 | chr6 | 32068580 | ||
chr6:32068586
|
T | C | 1 | a0017c0022 | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.6024A>G | p.Thr2008Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6190/13097 | 6024/12735 | 2008/4244 | chr6 | 32068586 | ||
chr6:32068673
|
G | A | 5 | a0005c0013a0005c0023a0005c0024others(2): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
synonymous_variant | LOW | c.5937C>T | p.Thr1979Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/44 | 6103/13097 | 5937/12735 | 1979/4244 | chr6 | 32068673 | ||
chr6:32068901
|
G | A | 2 | a0004c0008a0045c0063 | 11 | HG00741.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
synonymous_variant | LOW | c.5823C>T | p.Ser1941Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5989/13097 | 5823/12735 | 1941/4244 | chr6 | 32068901 | ||
chr6:32069045
|
C | T | 1 | a0094c0124 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.5679G>A | p.Thr1893Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/44 | 5845/13097 | 5679/12735 | 1893/4244 | chr6 | 32069045 | ||
chr6:32070206
|
G | C | 1 | a0003c0113 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.5199C>G | p.Ala1733Ala | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/44 | 5365/13097 | 5199/12735 | 1733/4244 | chr6 | 32070206 | ||
chr6:32079055
|
C | T | 3 | a0053c0119a0054c0122a0055c0123 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.4353G>A | p.Pro1451Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4519/13097 | 4353/12735 | 1451/4244 | chr6 | 32079055 | ||
chr6:32079076
|
G | A | 3 | a0002c0042a0033c0043a0043c0055 | 5 | HG01361.hp2 HG02145.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.4332C>T | p.His1444His | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4498/13097 | 4332/12735 | 1444/4244 | chr6 | 32079076 | ||
chr6:32079289
|
C | T | 1 | a0012c0099 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.4119G>A | p.Pro1373Pro | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/44 | 4285/13097 | 4119/12735 | 1373/4244 | chr6 | 32079289 | ||
chr6:32081600
|
G | A | 1 | a0025c0069 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.3810C>T | p.Thr1270Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3976/13097 | 3810/12735 | 1270/4244 | chr6 | 32081600 | ||
chr6:32081645
|
G | C | 1 | a0059c0074 | 1 | NA19081.hp2 | synonymous_variant | LOW | c.3765C>G | p.Arg1255Arg | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/44 | 3931/13097 | 3765/12735 | 1255/4244 | chr6 | 32081645 | ||
chr6:32084450
|
C | T | 1 | a0058c0073 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.3408G>A | p.Lys1136Lys | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/44 | 3574/13097 | 3408/12735 | 1136/4244 | chr6 | 32084450 | ||
chr6:32089353
|
T | C | 1 | a0060c0117 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2385A>G | p.Thr795Thr | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2551/13097 | 2385/12735 | 795/4244 | chr6 | 32089353 | ||
chr6:32089365
|
G | A | 2 | a0027c0052a0027c0125 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.2373C>T | p.Ser791Ser | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2539/13097 | 2373/12735 | 791/4244 | chr6 | 32089365 | ||
chr6:32089371
|
C | T | 1 | a0007c0005 | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
synonymous_variant | LOW | c.2367G>A | p.Gly789Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/44 | 2533/13097 | 2367/12735 | 789/4244 | chr6 | 32089371 | ||
chr6:32095831
|
G | T | 1 | a0009c0070 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.2022C>A | p.Gly674Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 2188/13097 | 2022/12735 | 674/4244 | chr6 | 32095831 | ||
chr6:32096119
|
G | A | 1 | a0016c0017 | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1900/13097 | 1734/12735 | 578/4244 | chr6 | 32096119 | ||
chr6:32096944
|
G | C | 2 | a0027c0052a0027c0125 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.909C>G | p.Gly303Gly | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/44 | 1075/13097 | 909/12735 | 303/4244 | chr6 | 32096944 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041186
|
C | T | 56 | a0001c0001t0002a0002c0012t0002a0002c0019t0002others(53): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*163G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 163 | chr6 | 32041186 | |||||
chr6:32041197
|
C | A | 1 | a0003c0048t0005 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 152 | chr6 | 32041197 | |||||
chr6:32041227
|
G | A | 3 | a0053c0119t0004a0054c0122t0004a0055c0123t0004 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*122C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 122 | chr6 | 32041227 | |||||
chr6:32041248
|
T | C | 1 | a0015c0016t0006 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 101 | chr6 | 32041248 | |||||
chr6:32041310
|
C | T | 1 | a0016c0017t0003 | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*39G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 44/44 | 39 | chr6 | 32041310 | |||||
chr6:32109327
|
G | A | 1 | a0092c0072t0007 | 1 | HG00140.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/44 | chr6 | 32109327 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32041502
|
T | C | 49 | a0002c0002t0001g0114a0008c0006t0001g0220a0008c0006t0001g0317others(46): Show | 51 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.12634-52A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041502 | ||||||
chr6:32041507
|
G | A | 16 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(13): Show | 17 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.12634-57C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041507 | ||||||
chr6:32041524
|
A | G | 43 | a0002c0042t0002g0076a0002c0042t0002g0142a0003c0003t0002g0351others(40): Show | 44 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.12634-74T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041524 | ||||||
chr6:32041574
|
C | T | 36 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(33): Show | 37 | HG00140.hp1 HG01167.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.12634-124G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041574 | ||||||
chr6:32041577
|
T | C | 34 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(31): Show | 35 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.12634-127A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041577 | ||||||
chr6:32041598
|
T | C | 33 | a0002c0012t0002g0077a0002c0042t0002g0142a0008c0006t0001g0220others(30): Show | 34 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.12634-148A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041598 | ||||||
chr6:32041608
|
C | T | 32 | a0002c0042t0002g0142a0008c0006t0001g0220a0008c0006t0001g0317others(29): Show | 33 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.12634-158G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041608 | ||||||
chr6:32041630
|
C | T | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.12633+141G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041630 | ||||||
chr6:32041679
|
A | G | 111 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.12633+92T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 43/43 | chr6 | 32041679 | ||||||
chr6:32042010
|
A | G | 4 | a0004c0062t0001g0176a0024c0032t0001g0180a0024c0032t0001g0190others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.12469+2T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 42/43 | chr6 | 32042010 | ||||||
chr6:32042239
|
G | C | 51 | a0002c0002t0001g0119a0002c0042t0002g0142a0002c0096t0001g0134others(48): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.12307+27C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 41/43 | chr6 | 32042239 | ||||||
chr6:32042402
|
G | A | 1 | a0064c0079t0001g0379 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12211-40C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042402 | ||||||
chr6:32042412
|
A | C | 53 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(50): Show | 54 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(51): Show |
intron_variant | MODIFIER | c.12210+43T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042412 | ||||||
chr6:32042415
|
C | CT | 53 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(50): Show | 54 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(51): Show |
intron_variant | MODIFIER | c.12210+39dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042415 | ||||||
chr6:32042419
|
C | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12210+36G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042419 | ||||||
chr6:32042450
|
C | T | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.12210+5G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 40/43 | chr6 | 32042450 | ||||||
chr6:32042684
|
C | T | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG00280.hp2 HG01123.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.12058+15G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/43 | chr6 | 32042684 | ||||||
chr6:32042688
|
C | T | 1 | a0001c0034t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12058+11G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 39/43 | chr6 | 32042688 | ||||||
chr6:32042848
|
G | C | 1 | a0016c0017t0003g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.11926-17C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/43 | chr6 | 32042848 | ||||||
chr6:32042945
|
G | C | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG01952.hp1 HG02027.hp1 HG02132.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.11925+6C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 38/43 | chr6 | 32042945 | ||||||
chr6:32043345
|
G | C | 1 | a0002c0002t0001g0130 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.11651-27C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/43 | chr6 | 32043345 | ||||||
chr6:32043427
|
G | C | 165 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.11650+10C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 36/43 | chr6 | 32043427 | ||||||
chr6:32043581
|
A | G | 206 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(203): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.11531-25T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043581 | ||||||
chr6:32043591
|
C | T | 4 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217others(1): Show | 4 | HG02738.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.11531-35G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043591 | ||||||
chr6:32043592
|
G | T | 79 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(76): Show | 85 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.11531-36C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043592 | ||||||
chr6:32043644
|
C | T | 23 | a0001c0001t0001g0260a0002c0002t0001g0111a0003c0048t0002g0360others(20): Show | 23 | HG00438.hp1 HG01123.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.11531-88G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043644 | ||||||
chr6:32043693
|
C | G | 21 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(18): Show | 21 | HG01952.hp1 HG02027.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.11530+56G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043693 | ||||||
chr6:32043703
|
G | A | 1 | a0083c0108t0002g0372 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.11530+46C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043703 | ||||||
chr6:32043711
|
G | C | 1 | a0044c0061t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.11530+38C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043711 | ||||||
chr6:32043712
|
G | A | 1 | a0083c0108t0002g0372 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.11530+37C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 35/43 | chr6 | 32043712 | ||||||
chr6:32043911
|
G | A | 1 | a0040c0047t0002g0361 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.11387-19C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043911 | ||||||
chr6:32043936
|
C | T | 2 | a0004c0011t0001g0182a0004c0011t0001g0184 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.11387-44G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043936 | ||||||
chr6:32043937
|
A | G | 186 | a0001c0007t0001g0310a0002c0012t0002g0077a0002c0097t0002g0039others(183): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.11387-45T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043937 | ||||||
chr6:32043959
|
A | T | 1 | a0042c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.11386+48T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043959 | ||||||
chr6:32043992
|
T | C | 3 | a0003c0003t0002g0244a0003c0003t0002g0251a0003c0003t0002g0313 | 3 | NA18612.hp2 NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.11386+15A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 34/43 | chr6 | 32043992 | ||||||
chr6:32044149
|
C | T | 4 | a0012c0015t0001g0326a0012c0015t0001g0332a0047c0065t0001g0346others(1): Show | 4 | HG03834.hp1 NA18948.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.11264-20G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044149 | ||||||
chr6:32044177
|
T | C | 140 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(137): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.11264-48A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044177 | ||||||
chr6:32044184
|
A | G | 161 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(158): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.11264-55T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044184 | ||||||
chr6:32044223
|
C | T | 11 | a0003c0003t0002g0353a0003c0003t0002g0354a0003c0003t0002g0362others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.11264-94G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044223 | ||||||
chr6:32044250
|
T | C | 1 | a0020c0025t0001g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11264-121A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044250 | ||||||
chr6:32044342
|
A | G | 52 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(49): Show | 58 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.11263+39T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 33/43 | chr6 | 32044342 | ||||||
chr6:32044732
|
G | A | 2 | a0041c0049t0002g0247a0041c0049t0002g0248 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.10928-16C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044732 | ||||||
chr6:32044780
|
G | A | 1 | a0035c0040t0002g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.10928-64C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044780 | ||||||
chr6:32044810
|
C | T | 41 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(38): Show | 45 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.10928-94G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 32/43 | chr6 | 32044810 | ||||||
chr6:32045352
|
A | G | 1 | a0054c0122t0004g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10607-26T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045352 | ||||||
chr6:32045503
|
G | A | 3 | a0029c0030t0001g0168a0029c0030t0001g0169a0029c0030t0001g0170 | 3 | NA18977.hp1 NA19004.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.10607-177C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045503 | ||||||
chr6:32045582
|
C | T | 1 | a0001c0034t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.10607-256G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045582 | ||||||
chr6:32045680
|
C | T | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.10607-354G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045680 | ||||||
chr6:32045723
|
T | C | 75 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(72): Show | 81 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.10607-397A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045723 | ||||||
chr6:32045777
|
C | T | 2 | a0049c0068t0002g0205a0061c0077t0002g0044 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.10606+398G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045777 | ||||||
chr6:32045850
|
G | A | 1 | a0008c0045t0001g0337 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10606+325C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045850 | ||||||
chr6:32045859
|
A | G | 1 | a0042c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10606+316T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045859 | ||||||
chr6:32045863
|
G | T | 7 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217others(4): Show | 8 | HG02083.hp2 HG02155.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.10606+312C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045863 | ||||||
chr6:32045892
|
C | A | 1 | a0074c0088t0001g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.10606+283G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045892 | ||||||
chr6:32045905
|
A | G | 1 | a0073c0087t0002g0030 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10606+270T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045905 | ||||||
chr6:32045913
|
T | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.10606+262A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045913 | ||||||
chr6:32045922
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.10606+253G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045922 | ||||||
chr6:32045981
|
T | A | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.10606+194A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 31/43 | chr6 | 32045981 | ||||||
chr6:32046679
|
C | T | 35 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(32): Show | 36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.10325-223G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046679 | ||||||
chr6:32046798
|
A | G | 237 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(234): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.10325-342T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046798 | ||||||
chr6:32046969
|
C | T | 1 | a0074c0088t0001g0131 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.10325-513G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32046969 | ||||||
chr6:32047051
|
G | A | 5 | a0019c0028t0002g0047a0019c0028t0002g0082a0019c0028t0002g0084others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.10325-595C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047051 | ||||||
chr6:32047058
|
G | A | 1 | a0040c0047t0002g0361 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.10325-602C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047058 | ||||||
chr6:32047180
|
C | A | 1 | a0079c0100t0001g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.10324+554G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047180 | ||||||
chr6:32047265
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.10324+469C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047265 | ||||||
chr6:32047549
|
C | T | 1 | a0042c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10324+185G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047549 | ||||||
chr6:32047651
|
C | T | 38 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(35): Show | 38 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.10324+83G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 30/43 | chr6 | 32047651 | ||||||
chr6:32048019
|
A | G | 57 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(54): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.10046-7T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048019 | ||||||
chr6:32048087
|
C | T | 13 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(10): Show | 13 | HG00438.hp1 HG02027.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.10046-75G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048087 | ||||||
chr6:32048109
|
C | T | 1 | a0009c0027t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.10046-97G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048109 | ||||||
chr6:32048320
|
G | T | 1 | a0008c0045t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10045+43C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 29/43 | chr6 | 32048320 | ||||||
chr6:32048743
|
C | T | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.9758-93G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048743 | ||||||
chr6:32048748
|
T | G | 1 | a0001c0001t0002g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.9758-98A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048748 | ||||||
chr6:32048891
|
G | C | 9 | a0009c0027t0001g0050a0009c0027t0001g0068a0009c0027t0001g0069others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.9758-241C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32048891 | ||||||
chr6:32049225
|
G | C | 1 | a0001c0001t0001g0304 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.9757+45C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32049225 | ||||||
chr6:32049258
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.9757+12G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 28/43 | chr6 | 32049258 | ||||||
chr6:32049596
|
GAGA | G | 6 | a0013c0014t0001g0292a0013c0014t0001g0293a0013c0014t0001g0301others(3): Show | 6 | HG02293.hp2 NA18956.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.9440-12_9440-10del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049596 | ||||||
chr6:32049744
|
C | T | 37 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(34): Show | 43 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.9440-157G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049744 | ||||||
chr6:32049745
|
G | A | 5 | a0016c0017t0003g0207a0016c0017t0003g0208a0016c0017t0003g0209others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9440-158C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049745 | ||||||
chr6:32049747
|
A | G | 5 | a0016c0017t0003g0207a0016c0017t0003g0208a0016c0017t0003g0209others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9440-160T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049747 | ||||||
chr6:32049763
|
A | G | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.9440-176T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049763 | ||||||
chr6:32049768
|
T | TG | 13 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(10): Show | 14 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.9440-182dupC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049768 | ||||||
chr6:32049830
|
G | C | 4 | a0035c0040t0002g0089a0036c0038t0002g0090a0036c0038t0002g0091others(1): Show | 4 | HG00741.hp1 HG03704.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.9439+168C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049830 | ||||||
chr6:32049839
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.9439+159C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 27/43 | chr6 | 32049839 | ||||||
chr6:32050410
|
A | G | 1 | a0003c0003t0001g0350 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.9116-89T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050410 | ||||||
chr6:32050426
|
C | A | 1 | a0061c0077t0002g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.9116-105G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050426 | ||||||
chr6:32050462
|
C | T | 20 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(17): Show | 20 | HG00438.hp1 HG00735.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.9116-141G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050462 | ||||||
chr6:32050517
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.9116-196T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050517 | ||||||
chr6:32050568
|
C | G | 5 | a0016c0017t0003g0207a0016c0017t0003g0208a0016c0017t0003g0209others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.9116-247G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050568 | ||||||
chr6:32050592
|
T | C | 2 | a0001c0007t0001g0310a0070c0090t0001g0136 | 2 | HG00673.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.9116-271A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050592 | ||||||
chr6:32050633
|
G | A | 10 | a0006c0004t0001g0001a0006c0004t0001g0185a0006c0004t0001g0195others(7): Show | 14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.9116-312C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050633 | ||||||
chr6:32050694
|
G | A | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.9116-373C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050694 | ||||||
chr6:32050796
|
A | C | 35 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(32): Show | 36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.9116-475T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32050796 | ||||||
chr6:32051094
|
C | T | 1 | a0083c0108t0002g0372 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.9116-773G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051094 | ||||||
chr6:32051419
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9116-1098C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051419 | ||||||
chr6:32051458
|
A | C | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.9116-1137T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051458 | ||||||
chr6:32051605
|
A | C | 1 | a0001c0034t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.9115+1065T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051605 | ||||||
chr6:32051735
|
T | C | 7 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0321others(4): Show | 7 | HG00140.hp1 HG02080.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.9115+935A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051735 | ||||||
chr6:32051969
|
G | C | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.9115+701C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051969 | ||||||
chr6:32051992
|
G | A | 60 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(57): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.9115+678C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32051992 | ||||||
chr6:32052070
|
T | C | 6 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.9115+600A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052070 | ||||||
chr6:32052169
|
C | T | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.9115+501G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052169 | ||||||
chr6:32052204
|
C | A | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.9115+466G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052204 | ||||||
chr6:32052237
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9115+433C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052237 | ||||||
chr6:32052450
|
C | CA | 20 | a0001c0001t0001g0109a0001c0001t0001g0159a0001c0001t0001g0160others(17): Show | 22 | HG00140.hp1 HG02080.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.9115+219dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052450 | ||||||
chr6:32052450
|
CA | C | 10 | a0001c0001t0001g0272a0001c0001t0001g0295a0001c0007t0001g0282others(7): Show | 10 | HG01934.hp1 HG01975.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.9115+219delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052450 | ||||||
chr6:32052461
|
A | G | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.9115+209T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052461 | ||||||
chr6:32052557
|
T | C | 1 | a0098c0056t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.9115+113A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 26/43 | chr6 | 32052557 | ||||||
chr6:32053067
|
G | A | 29 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(26): Show | 30 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.8792-74C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053067 | ||||||
chr6:32053333
|
G | C | 1 | a0049c0068t0002g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8791+55C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053333 | ||||||
chr6:32053353
|
C | T | 22 | a0009c0020t0001g0046a0009c0020t0001g0070a0009c0020t0001g0071others(19): Show | 22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8791+35G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 25/43 | chr6 | 32053353 | ||||||
chr6:32053852
|
T | C | 1 | a0044c0061t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8468-141A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053852 | ||||||
chr6:32053885
|
C | T | 21 | a0009c0020t0001g0046a0009c0020t0001g0070a0009c0020t0001g0071others(18): Show | 21 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.8468-174G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053885 | ||||||
chr6:32053913
|
A | C | 5 | a0004c0011t0001g0192a0004c0062t0001g0176a0024c0032t0001g0180others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.8468-202T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053913 | ||||||
chr6:32053999
|
G | C | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.8468-288C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32053999 | ||||||
chr6:32054061
|
A | T | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.8468-350T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054061 | ||||||
chr6:32054075
|
A | G | 37 | a0004c0011t0001g0162a0004c0011t0001g0182a0004c0011t0001g0183others(34): Show | 39 | HG00558.hp1 HG00738.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.8468-364T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054075 | ||||||
chr6:32054182
|
C | T | 1 | a0008c0006t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.8468-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054182 | ||||||
chr6:32054185
|
C | G | 6 | a0005c0024t0001g0221a0005c0024t0001g0222a0005c0024t0001g0223others(3): Show | 6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.8468-474G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054185 | ||||||
chr6:32054199
|
A | G | 22 | a0009c0020t0001g0046a0009c0020t0001g0070a0009c0020t0001g0071others(19): Show | 22 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8468-488T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054199 | ||||||
chr6:32054212
|
GC | G | 2 | a0020c0025t0001g0005a0020c0025t0001g0174 | 4 | HG02129.hp2 HG03471.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.8468-502delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054212 | ||||||
chr6:32054370
|
A | G | 15 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(12): Show | 17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.8468-659T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054370 | ||||||
chr6:32054852
|
A | G | 1 | a0049c0068t0002g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8467+999T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054852 | ||||||
chr6:32054860
|
C | G | 1 | a0002c0002t0001g0008 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.8467+991G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32054860 | ||||||
chr6:32055056
|
T | G | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.8467+795A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055056 | ||||||
chr6:32055121
|
C | T | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.8467+730G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055121 | ||||||
chr6:32055152
|
C | T | 1 | a0001c0007t0001g0310 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.8467+699G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055152 | ||||||
chr6:32055202
|
C | A | 2 | a0064c0079t0001g0379a0093c0116t0001g0378 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.8467+649G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055202 | ||||||
chr6:32055234
|
T | A | 21 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(18): Show | 23 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.8467+617A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055234 | ||||||
chr6:32055348
|
C | T | 1 | a0009c0070t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8467+503G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055348 | ||||||
chr6:32055366
|
G | A | 2 | a0009c0020t0001g0046a0066c0091t0002g0143 | 2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.8467+485C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055366 | ||||||
chr6:32055648
|
C | T | 14 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(11): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.8467+203G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055648 | ||||||
chr6:32055716
|
A | G | 2 | a0031c0051t0001g0025a0031c0051t0001g0026 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.8467+135T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055716 | ||||||
chr6:32055754
|
C | A | 6 | a0005c0024t0001g0221a0005c0024t0001g0222a0005c0024t0001g0223others(3): Show | 6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.8467+97G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055754 | ||||||
chr6:32055766
|
G | A | 2 | a0009c0020t0001g0046a0066c0091t0002g0143 | 2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.8467+85C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 24/43 | chr6 | 32055766 | ||||||
chr6:32056277
|
T | A | 1 | a0001c0109t0001g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8144-103A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/43 | chr6 | 32056277 | ||||||
chr6:32056378
|
T | C | 1 | a0055c0123t0004g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8144-204A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 23/43 | chr6 | 32056378 | ||||||
chr6:32057004
|
C | T | 3 | a0002c0002t0001g0114a0002c0002t0001g0130a0002c0002t0001g0150 | 3 | HG02056.hp1 NA18971.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.7826-101G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057004 | ||||||
chr6:32057005
|
G | A | 13 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(10): Show | 13 | HG00438.hp1 HG02027.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.7826-102C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057005 | ||||||
chr6:32057055
|
T | C | 239 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(236): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.7826-152A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057055 | ||||||
chr6:32057281
|
C | A | 12 | a0005c0013t0001g0230a0005c0013t0001g0233a0005c0013t0001g0234others(9): Show | 12 | HG00438.hp1 HG02132.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.7826-378G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057281 | ||||||
chr6:32057379
|
A | C | 1 | a0037c0041t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7826-476T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057379 | ||||||
chr6:32057524
|
G | A | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7825+534C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057524 | ||||||
chr6:32057538
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.7825+520G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057538 | ||||||
chr6:32057539
|
T | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.7825+519A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057539 | ||||||
chr6:32057549
|
C | T | 60 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(57): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.7825+509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057549 | ||||||
chr6:32057633
|
ACT | A | 35 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(32): Show | 36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.7825+423_7825+424d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057633 | ||||||
chr6:32057663
|
T | C | 2 | a0064c0079t0001g0379a0093c0116t0001g0378 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.7825+395A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057663 | ||||||
chr6:32057778
|
C | A | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.7825+280G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32057778 | ||||||
chr6:32058031
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.7825+27T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 22/43 | chr6 | 32058031 | ||||||
chr6:32058435
|
CA | C | 14 | a0022c0029t0001g0157a0022c0029t0001g0164a0022c0029t0001g0167others(11): Show | 14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.7493-46delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058435 | ||||||
chr6:32058480
|
T | C | 373 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(370): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.7493-90A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058480 | ||||||
chr6:32058551
|
C | T | 2 | a0060c0117t0002g0149a0068c0095t0001g0289 | 2 | HG01346.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.7493-161G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058551 | ||||||
chr6:32058629
|
CAT | C | 6 | a0026c0033t0002g0152a0026c0033t0002g0153a0026c0033t0002g0154others(3): Show | 6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.7493-241_7493-240d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058629 | ||||||
chr6:32058733
|
T | G | 1 | a0066c0091t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-343A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058733 | ||||||
chr6:32058736
|
A | C | 1 | a0066c0091t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-346T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058736 | ||||||
chr6:32058819
|
T | A | 1 | a0066c0091t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-429A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058819 | ||||||
chr6:32058873
|
T | A | 1 | a0066c0091t0002g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7493-483A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058873 | ||||||
chr6:32058900
|
G | A | 1 | a0004c0008t0001g0187 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7493-510C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32058900 | ||||||
chr6:32059031
|
G | A | 30 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(27): Show | 31 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.7493-641C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059031 | ||||||
chr6:32059032
|
G | C | 1 | a0022c0029t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7493-642C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059032 | ||||||
chr6:32059131
|
A | G | 1 | a0055c0123t0004g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7493-741T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059131 | ||||||
chr6:32059418
|
C | CA | 61 | a0001c0001t0001g0243a0001c0001t0001g0273a0002c0002t0001g0128others(58): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.7493-1029dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059418 | ||||||
chr6:32059418
|
CA | C | 20 | a0001c0001t0001g0106a0001c0007t0001g0285a0002c0002t0001g0124others(17): Show | 22 | NA18612.hp1 NA18945.hp2 NA18950.hp1 others(19): Show |
intron_variant | MODIFIER | c.7493-1029delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059418 | ||||||
chr6:32059669
|
A | T | 5 | a0008c0006t0001g0318a0008c0006t0001g0320a0008c0006t0001g0338others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.7493-1279T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059669 | ||||||
chr6:32059784
|
T | C | 1 | a0076c0080t0001g0380 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7493-1394A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059784 | ||||||
chr6:32059889
|
C | T | 1 | a0022c0059t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.7493-1499G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059889 | ||||||
chr6:32059983
|
T | C | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7492+1414A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32059983 | ||||||
chr6:32060105
|
C | T | 1 | a0005c0013t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.7492+1292G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060105 | ||||||
chr6:32060300
|
C | CCAGCCTG others(62): Show |
1 | a0022c0029t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7492+1096_7492+109 others(73): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060300 | ||||||
chr6:32060300
|
C | CCAGCCTG others(61): Show |
13 | a0022c0029t0001g0157a0022c0029t0001g0164a0022c0059t0001g0165others(10): Show | 13 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.7492+1029_7492+109 others(72): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060300 | ||||||
chr6:32060332
|
C | CA | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.7492+1064dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060332 | ||||||
chr6:32060332
|
CA | C | 14 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(11): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.7492+1064delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060332 | ||||||
chr6:32060372
|
G | C | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.7492+1025C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060372 | ||||||
chr6:32060420
|
TATATATT others(18): Show |
T | 1 | a0072c0086t0001g0122 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7492+952_7492+976d others(27): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060420 | ||||||
chr6:32060644
|
T | C | 1 | a0068c0095t0001g0289 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.7492+753A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060644 | ||||||
chr6:32060732
|
G | A | 1 | a0001c0034t0001g0265 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.7492+665C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32060732 | ||||||
chr6:32061173
|
T | C | 2 | a0004c0011t0001g0182a0004c0011t0001g0184 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7492+224A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061173 | ||||||
chr6:32061228
|
C | G | 2 | a0010c0084t0002g0041a0048c0066t0002g0175 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.7492+169G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061228 | ||||||
chr6:32061247
|
C | T | 2 | a0030c0031t0001g0206a0060c0117t0002g0149 | 2 | HG02615.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.7492+150G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061247 | ||||||
chr6:32061283
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7492+114C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061283 | ||||||
chr6:32061389
|
C | T | 3 | a0009c0020t0001g0070a0009c0020t0001g0071a0009c0020t0001g0072 | 3 | HG00597.hp2 HG02132.hp2 NA18951.hp2 |
splice_region_variant&intron_variant | LOW | c.7492+8G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 21/43 | chr6 | 32061389 | ||||||
chr6:32061751
|
G | A | 1 | a0003c0003t0002g0368 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7169-31C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061751 | ||||||
chr6:32061968
|
A | G | 4 | a0001c0001t0001g0307a0009c0020t0001g0070a0009c0020t0001g0071others(1): Show | 4 | HG00597.hp2 HG02056.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.7168+189T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061968 | ||||||
chr6:32061969
|
T | C | 2 | a0054c0122t0004g0228a0055c0123t0004g0227 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7168+188A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061969 | ||||||
chr6:32061992
|
G | A | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7168+165C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32061992 | ||||||
chr6:32062072
|
G | A | 60 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(57): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.7168+85C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062072 | ||||||
chr6:32062138
|
G | T | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.7168+19C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062138 | ||||||
chr6:32062146
|
C | T | 1 | a0022c0029t0001g0167 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7168+11G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062146 | ||||||
chr6:32062152
|
C | T | 10 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(7): Show | 11 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.7168+5G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 20/43 | chr6 | 32062152 | ||||||
chr6:32062507
|
G | A | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.6842-24C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062507 | ||||||
chr6:32062712
|
G | C | 1 | a0002c0002t0001g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6842-229C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062712 | ||||||
chr6:32062923
|
C | T | 8 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(5): Show | 10 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6842-440G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32062923 | ||||||
chr6:32063045
|
T | C | 1 | a0003c0003t0002g0374 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6842-562A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063045 | ||||||
chr6:32063047
|
C | T | 10 | a0012c0015t0001g0326a0012c0015t0001g0327a0012c0015t0001g0330others(7): Show | 10 | HG02622.hp1 HG02735.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.6842-564G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063047 | ||||||
chr6:32063142
|
C | G | 1 | a0096c0057t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6842-659G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063142 | ||||||
chr6:32063197
|
G | C | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6842-714C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063197 | ||||||
chr6:32063404
|
G | GA | 19 | a0001c0001t0001g0297a0005c0013t0001g0040a0005c0013t0001g0230others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6842-922dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063404 | ||||||
chr6:32063404
|
GA | G | 26 | a0001c0007t0001g0285a0010c0010t0001g0017a0010c0010t0002g0006others(23): Show | 28 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.6842-922delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063404 | ||||||
chr6:32063479
|
G | A | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6842-996C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063479 | ||||||
chr6:32063534
|
T | C | 2 | a0001c0001t0002g0271a0085c0106t0002g0275 | 2 | HG00099.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.6842-1051A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32063534 | ||||||
chr6:32064127
|
G | A | 14 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(11): Show | 14 | HG00140.hp1 HG01884.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.6841+694C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064127 | ||||||
chr6:32064140
|
G | C | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.6841+681C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064140 | ||||||
chr6:32064235
|
C | T | 1 | a0082c0112t0002g0349 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6841+586G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064235 | ||||||
chr6:32064238
|
G | C | 1 | a0003c0048t0002g0360 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6841+583C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064238 | ||||||
chr6:32064324
|
C | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6841+497G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064324 | ||||||
chr6:32064362
|
G | A | 35 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(32): Show | 36 | HG00140.hp1 HG01243.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.6841+459C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064362 | ||||||
chr6:32064426
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6841+395G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064426 | ||||||
chr6:32064428
|
G | C | 83 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.6841+393C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064428 | ||||||
chr6:32064434
|
G | T | 3 | a0023c0036t0002g0011a0023c0053t0002g0161a0042c0054t0002g0158 | 4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.6841+387C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064434 | ||||||
chr6:32064529
|
C | T | 60 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(57): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.6841+292G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064529 | ||||||
chr6:32064572
|
C | T | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6841+249G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064572 | ||||||
chr6:32064644
|
C | T | 66 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(63): Show | 72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.6841+177G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 19/43 | chr6 | 32064644 | ||||||
chr6:32065230
|
G | A | 83 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.6545-113C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065230 | ||||||
chr6:32065674
|
C | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6545-557G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065674 | ||||||
chr6:32065682
|
C | T | 1 | a0012c0015t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6545-565G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065682 | ||||||
chr6:32065770
|
G | A | 2 | a0009c0020t0001g0073a0094c0124t0002g0066 | 2 | NA19007.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6545-653C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065770 | ||||||
chr6:32065839
|
G | A | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.6545-722C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065839 | ||||||
chr6:32065852
|
G | C | 1 | a0002c0002t0001g0008 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6545-735C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32065852 | ||||||
chr6:32066167
|
A | G | 349 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(346): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.6545-1050T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066167 | ||||||
chr6:32066292
|
G | C | 1 | a0012c0015t0001g0332 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6545-1175C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066292 | ||||||
chr6:32066315
|
G | C | 2 | a0003c0048t0002g0360a0003c0048t0005g0370 | 2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6545-1198C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066315 | ||||||
chr6:32066399
|
A | AAATC | 24 | a0002c0019t0002g0003a0002c0019t0002g0059a0002c0019t0002g0060others(21): Show | 26 | HG00423.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.6544+1258_6544+126 others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066399 | ||||||
chr6:32066399
|
AAATC | A | 6 | a0001c0001t0001g0257a0002c0002t0001g0113a0020c0025t0001g0005others(3): Show | 8 | HG01255.hp2 HG02071.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.6544+1258_6544+126 others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066399 | ||||||
chr6:32066629
|
A | G | 1 | a0022c0029t0001g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6544+1032T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32066629 | ||||||
chr6:32067074
|
TAAAAAGA others(6): Show |
T | 3 | a0023c0036t0002g0011a0023c0053t0002g0161a0042c0054t0002g0158 | 4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.6544+574_6544+586d others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067074 | ||||||
chr6:32067084
|
G | GAAAGA | 255 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(252): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.6544+572_6544+576d others(7): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067084 | ||||||
chr6:32067094
|
AATGAAAG | A | 3 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+560_6544+566d others(9): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067094 | ||||||
chr6:32067108
|
A | T | 3 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+553T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067108 | ||||||
chr6:32067111
|
AAG | A | 3 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+548_6544+549d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067111 | ||||||
chr6:32067124
|
A | AAAGG | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0034t0001g0265 | 3 | HG01169.hp2 NA18961.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.6544+533_6544+536d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067124 | ||||||
chr6:32067124
|
A | G | 9 | a0002c0019t0002g0003a0002c0019t0002g0059a0002c0019t0002g0060others(6): Show | 11 | HG00735.hp2 HG01255.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+537T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067124 | ||||||
chr6:32067127
|
GGAAGGA | G | 3 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+533d others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067127 | ||||||
chr6:32067128
|
G | GAAGAAGA others(4): Show |
1 | a0034c0039t0002g0078 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.6544+532_6544+533i others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | ||||||
chr6:32067128
|
G | GAAGAAGA others(3): Show |
1 | a0012c0099t0001g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6544+532_6544+533i others(12): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | ||||||
chr6:32067128
|
G | GAAGAAGA others(15): Show |
1 | a0002c0002t0001g0111 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6544+532_6544+533i others(24): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067128 | ||||||
chr6:32067132
|
G | A | 4 | a0001c0007t0001g0287a0002c0002t0001g0111a0012c0099t0001g0333others(1): Show | 4 | HG03209.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.6544+529C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGA | 36 | a0001c0001t0001g0031a0001c0001t0001g0257a0001c0001t0001g0294others(33): Show | 37 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.6544+525_6544+528d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(1): Show |
48 | a0001c0001t0001g0226a0001c0001t0001g0258a0001c0001t0001g0259others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.6544+521_6544+528d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(5): Show |
66 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0249others(63): Show | 70 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.6544+517_6544+528d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(9): Show |
30 | a0001c0001t0001g0160a0002c0002t0001g0009a0002c0002t0001g0010others(27): Show | 32 | HG00423.hp1 HG00738.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.6544+513_6544+528d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(13): Show |
12 | a0001c0001t0001g0300a0002c0002t0001g0120a0002c0002t0001g0121others(9): Show | 12 | HG00597.hp2 HG01517.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6544+509_6544+528d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(17): Show |
4 | a0003c0003t0002g0048a0003c0003t0002g0362a0015c0016t0002g0357others(1): Show | 4 | HG00438.hp2 NA18972.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.6544+505_6544+528d others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAAG others(21): Show |
2 | a0002c0002t0001g0118a0037c0041t0001g0146 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6544+501_6544+528d others(30): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGAAGA others(12): Show |
1 | a0040c0047t0002g0361 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(21): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(1): Show |
10 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0110others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(5): Show |
9 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0107others(6): Show | 9 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(9): Show |
10 | a0001c0001t0001g0106a0001c0001t0001g0151a0010c0010t0002g0006others(7): Show | 11 | HG01074.hp1 HG01099.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+528_6544+529i others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(13): Show |
3 | a0001c0001t0001g0102a0035c0040t0002g0089a0039c0046t0001g0263 | 3 | HG00741.hp1 HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(17): Show |
1 | a0063c0098t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(21): Show |
2 | a0010c0010t0002g0029a0038c0044t0001g0329 | 2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(30): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(5): Show |
2 | a0054c0122t0004g0228a0055c0123t0004g0227 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6544+528_6544+529i others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAAGGAAG others(17): Show |
1 | a0053c0119t0004g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAGAAAGA others(4): Show |
1 | a0015c0016t0002g0356 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.6544+528_6544+529i others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
G | GAGAAGAA others(3): Show |
1 | a0001c0001t0001g0269 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6544+528_6544+529i others(12): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
GAAGA | G | 6 | a0001c0007t0001g0282a0008c0006t0001g0318a0008c0006t0001g0320others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.6544+525_6544+528d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
GAAGAAAG others(1): Show |
G | 33 | a0005c0013t0001g0040a0005c0024t0001g0221a0005c0024t0001g0222others(30): Show | 36 | HG00140.hp1 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.6544+521_6544+528d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
GAAGAAAG others(5): Show |
G | 17 | a0005c0013t0001g0230a0005c0013t0001g0233a0005c0013t0001g0234others(14): Show | 17 | HG00438.hp1 HG00738.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.6544+517_6544+528d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067132
|
GAAGAAAG others(9): Show |
G | 14 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(11): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.6544+513_6544+528d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067132 | ||||||
chr6:32067140
|
A | G | 1 | a0001c0007t0001g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6544+521T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067140 | ||||||
chr6:32067143
|
G | GAA | 11 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6544+516_6544+517d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067143 | ||||||
chr6:32067144
|
A | G | 7 | a0005c0013t0001g0040a0005c0024t0001g0221a0005c0024t0001g0222others(4): Show | 7 | HG01952.hp1 HG02027.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.6544+517T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067144 | ||||||
chr6:32067145
|
AAG | A | 25 | a0004c0008t0001g0315a0004c0011t0001g0162a0004c0011t0001g0178others(22): Show | 29 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.6544+514_6544+515d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067145 | ||||||
chr6:32067148
|
A | G | 15 | a0005c0013t0001g0230a0005c0013t0001g0233a0005c0013t0001g0234others(12): Show | 15 | HG00438.hp1 HG02132.hp1 HG03491.hp1 others(12): Show |
intron_variant | MODIFIER | c.6544+513T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067148 | ||||||
chr6:32067152
|
A | AAAGAAAG others(8): Show |
1 | a0002c0094t0001g0129 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6544+494_6544+508d others(17): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067152 | ||||||
chr6:32067152
|
A | G | 3 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.6544+509T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067152 | ||||||
chr6:32067163
|
G | GAAAGAAA others(9): Show |
1 | a0009c0027t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6544+497_6544+498i others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067163 | ||||||
chr6:32067381
|
AAG | A | 9 | a0009c0027t0001g0050a0009c0027t0001g0068a0009c0027t0001g0069others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.6544+278_6544+279d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067381 | ||||||
chr6:32067482
|
C | T | 1 | a0010c0010t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6544+179G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067482 | ||||||
chr6:32067650
|
T | C | 64 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(61): Show | 71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.6544+11A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067650 | ||||||
chr6:32067653
|
A | T | 3 | a0001c0001t0001g0249a0041c0049t0002g0247a0041c0049t0002g0248 | 3 | HG00639.hp2 HG01515.hp2 HG01517.hp2 |
splice_region_variant&intron_variant | LOW | c.6544+8T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 18/43 | chr6 | 32067653 | ||||||
chr6:32068084
|
A | G | 12 | a0003c0003t0002g0353a0003c0003t0002g0354a0003c0003t0002g0364others(9): Show | 12 | HG00423.hp1 HG02040.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.6221-100T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068084 | ||||||
chr6:32068300
|
C | A | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6220+90G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068300 | ||||||
chr6:32068335
|
G | A | 1 | a0005c0024t0001g0255 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6220+55C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068335 | ||||||
chr6:32068358
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6220+32G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 17/43 | chr6 | 32068358 | ||||||
chr6:32068753
|
C | T | 1 | a0012c0099t0001g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5903-46G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 16/43 | chr6 | 32068753 | ||||||
chr6:32069320
|
C | T | 1 | a0061c0077t0002g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5588-184G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/43 | chr6 | 32069320 | ||||||
chr6:32069372
|
G | A | 1 | a0017c0022t0002g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5587+181C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 15/43 | chr6 | 32069372 | ||||||
chr6:32070003
|
G | A | 1 | a0028c0035t0001g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5278+124C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070003 | ||||||
chr6:32070023
|
C | T | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5278+104G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070023 | ||||||
chr6:32070087
|
G | A | 1 | a0042c0054t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5278+40C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 14/43 | chr6 | 32070087 | ||||||
chr6:32070498
|
GC | G | 14 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(11): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4991-85delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070498 | ||||||
chr6:32070773
|
C | T | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.4991-359G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070773 | ||||||
chr6:32070788
|
C | T | 1 | a0053c0119t0004g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4991-374G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070788 | ||||||
chr6:32070818
|
C | T | 1 | a0088c0104t0001g0306 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4991-404G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070818 | ||||||
chr6:32070902
|
G | A | 4 | a0006c0004t0001g0197a0006c0004t0001g0198a0006c0004t0001g0199others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4991-488C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070902 | ||||||
chr6:32070923
|
C | T | 81 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.4991-509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32070923 | ||||||
chr6:32071455
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4990+535A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071455 | ||||||
chr6:32071474
|
A | G | 1 | a0014c0018t0002g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4990+516T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071474 | ||||||
chr6:32071526
|
C | T | 1 | a0009c0020t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4990+464G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071526 | ||||||
chr6:32071578
|
C | CT | 152 | a0001c0001t0001g0309a0002c0019t0002g0003a0002c0019t0002g0059others(149): Show | 161 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.4990+411dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071578 | ||||||
chr6:32071578
|
C | CTT | 79 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.4990+410_4990+411d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071578 | ||||||
chr6:32071676
|
C | G | 1 | a0095c0064t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4990+314G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071676 | ||||||
chr6:32071873
|
A | G | 1 | a0005c0024t0001g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4990+117T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 13/43 | chr6 | 32071873 | ||||||
chr6:32072408
|
T | C | 1 | a0008c0045t0001g0337 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4682-110A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072408 | ||||||
chr6:32072632
|
G | A | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4682-334C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072632 | ||||||
chr6:32072707
|
T | C | 22 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(19): Show | 22 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.4682-409A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072707 | ||||||
chr6:32072827
|
C | T | 32 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(29): Show | 32 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.4682-529G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072827 | ||||||
chr6:32072859
|
G | T | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4682-561C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32072859 | ||||||
chr6:32073023
|
T | C | 6 | a0026c0033t0002g0152a0026c0033t0002g0153a0026c0033t0002g0154others(3): Show | 6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.4681+624A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073023 | ||||||
chr6:32073102
|
T | G | 2 | a0031c0051t0001g0025a0031c0051t0001g0026 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.4681+545A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073102 | ||||||
chr6:32073154
|
A | G | 86 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(83): Show | 93 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.4681+493T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073154 | ||||||
chr6:32073216
|
G | A | 7 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217others(4): Show | 8 | HG01243.hp1 HG02738.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.4681+431C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073216 | ||||||
chr6:32073266
|
A | C | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.4681+381T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073266 | ||||||
chr6:32073293
|
G | C | 1 | a0078c0075t0002g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4681+354C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073293 | ||||||
chr6:32073516
|
G | A | 1 | a0009c0020t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4681+131C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073516 | ||||||
chr6:32073596
|
G | A | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4681+51C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 12/43 | chr6 | 32073596 | ||||||
chr6:32074154
|
C | G | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4376-202G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074154 | ||||||
chr6:32074214
|
C | T | 6 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4376-262G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074214 | ||||||
chr6:32074273
|
C | T | 1 | a0008c0006t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4376-321G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074273 | ||||||
chr6:32074423
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.4376-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074423 | ||||||
chr6:32074458
|
T | A | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4376-506A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074458 | ||||||
chr6:32074545
|
T | C | 313 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(310): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.4376-593A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074545 | ||||||
chr6:32074568
|
G | A | 1 | a0006c0004t0001g0201 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4376-616C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074568 | ||||||
chr6:32074971
|
C | T | 1 | a0002c0012t0002g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4376-1019G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32074971 | ||||||
chr6:32075189
|
C | G | 2 | a0030c0031t0001g0171a0030c0031t0001g0206 | 2 | NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4376-1237G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075189 | ||||||
chr6:32075380
|
T | C | 4 | a0010c0010t0002g0006a0010c0010t0002g0024a0010c0010t0002g0027others(1): Show | 5 | HG01074.hp1 HG01099.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.4376-1428A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075380 | ||||||
chr6:32075533
|
G | A | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4376-1581C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075533 | ||||||
chr6:32075879
|
C | CT | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4376-1928dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32075879 | ||||||
chr6:32076209
|
TGCTGGTG others(5): Show |
T | 1 | a0001c0001t0001g0298 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4376-2269_4376-225 others(16): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076209 | ||||||
chr6:32076217
|
G | T | 1 | a0060c0117t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4376-2265C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076217 | ||||||
chr6:32076292
|
C | T | 1 | a0008c0006t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4376-2340G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076292 | ||||||
chr6:32076395
|
G | C | 3 | a0064c0079t0001g0379a0076c0080t0001g0380a0093c0116t0001g0378 | 3 | HG01891.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4376-2443C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076395 | ||||||
chr6:32076538
|
A | G | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4375+2495T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076538 | ||||||
chr6:32076539
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.4375+2494G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076539 | ||||||
chr6:32076784
|
C | G | 1 | a0010c0010t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4375+2249G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32076784 | ||||||
chr6:32077057
|
G | C | 35 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(32): Show | 40 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.4375+1976C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077057 | ||||||
chr6:32077074
|
C | T | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.4375+1959G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077074 | ||||||
chr6:32077075
|
A | G | 1 | a0015c0016t0006g0376 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4375+1958T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077075 | ||||||
chr6:32077104
|
T | TGCCTGAC others(4): Show |
1 | a0082c0112t0002g0349 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4375+1918_4375+192 others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077104 | ||||||
chr6:32077449
|
T | A | 17 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(14): Show | 19 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.4375+1584A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077449 | ||||||
chr6:32077518
|
A | G | 3 | a0023c0036t0002g0011a0023c0053t0002g0161a0042c0054t0002g0158 | 4 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375+1515T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077518 | ||||||
chr6:32077670
|
T | G | 1 | a0006c0004t0001g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4375+1363A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077670 | ||||||
chr6:32077797
|
C | T | 1 | a0003c0003t0002g0352 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4375+1236G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077797 | ||||||
chr6:32077957
|
G | A | 1 | a0096c0057t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4375+1076C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32077957 | ||||||
chr6:32078071
|
A | AGAGAAAG others(8): Show |
2 | a0003c0113t0002g0369a0040c0047t0002g0361 | 2 | HG02083.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4375+961_4375+962i others(17): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078071 | ||||||
chr6:32078073
|
G | A | 2 | a0003c0113t0002g0369a0040c0047t0002g0361 | 2 | HG02083.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4375+960C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
G | GAGAA | 73 | a0001c0001t0001g0298a0002c0002t0001g0008a0002c0002t0001g0009others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.4375+956_4375+959d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
G | GAGAAAGA others(1): Show |
40 | a0002c0002t0001g0113a0002c0002t0001g0123a0002c0002t0001g0124others(37): Show | 43 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.4375+952_4375+959d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
G | GAGAAAGA others(5): Show |
12 | a0003c0003t0002g0353a0003c0048t0002g0360a0007c0005t0002g0042others(9): Show | 14 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.4375+948_4375+959d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
G | GAGAAAGA others(9): Show |
4 | a0002c0012t0002g0062a0002c0012t0002g0063a0008c0006t0001g0220others(1): Show | 4 | HG02293.hp1 HG02300.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375+944_4375+959d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
G | GAGAAAGA others(13): Show |
1 | a0002c0012t0002g0064 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4375+940_4375+959d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAA | G | 28 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0007t0001g0287others(25): Show | 30 | HG00673.hp1 HG00735.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.4375+956_4375+959d others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAAAGA others(1): Show |
G | 25 | a0001c0001t0001g0156a0001c0001t0001g0226a0001c0001t0001g0294others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.4375+952_4375+959d others(10): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAAAGA others(5): Show |
G | 31 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0001g0109others(28): Show | 33 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.4375+948_4375+959d others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAAAGA others(9): Show |
G | 26 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(23): Show | 26 | HG00280.hp2 HG01123.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.4375+944_4375+959d others(18): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAAAGA others(13): Show |
G | 16 | a0001c0001t0001g0159a0001c0001t0001g0160a0005c0013t0001g0040others(13): Show | 16 | HG00438.hp1 HG02027.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4375+940_4375+959d others(22): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078073
|
GAGAAAGA others(17): Show |
G | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4375+936_4375+959d others(26): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078073 | ||||||
chr6:32078075
|
GAAAGAAA others(10): Show |
G | 1 | a0005c0013t0001g0233 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4375+941_4375+957d others(19): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078075 | ||||||
chr6:32078093
|
AAGAAAG | A | 3 | a0006c0004t0001g0197a0006c0004t0001g0198a0006c0004t0001g0199 | 3 | HG01167.hp2 HG01169.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4375+934_4375+939d others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078093 | ||||||
chr6:32078095
|
G | GAA | 3 | a0004c0008t0001g0138a0030c0031t0001g0166a0049c0068t0002g0205 | 3 | HG03516.hp1 NA18939.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4375+936_4375+937d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078095 | ||||||
chr6:32078097
|
AAG | A | 59 | a0004c0008t0001g0033a0004c0008t0001g0177a0004c0008t0001g0186others(56): Show | 66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.4375+934_4375+935d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078097 | ||||||
chr6:32078133
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4375+900T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078133 | ||||||
chr6:32078309
|
G | A | 1 | a0098c0056t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4375+724C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078309 | ||||||
chr6:32078447
|
C | CA | 114 | a0001c0001t0001g0108a0001c0001t0001g0243a0001c0001t0001g0276others(111): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.4375+585dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | ||||||
chr6:32078447
|
C | CAA | 17 | a0002c0002t0001g0125a0002c0002t0001g0126a0002c0094t0001g0129others(14): Show | 17 | HG00741.hp2 HG02080.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.4375+584_4375+585d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | ||||||
chr6:32078447
|
CA | C | 20 | a0001c0001t0001g0109a0001c0001t0001g0159a0001c0001t0001g0300others(17): Show | 21 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.4375+585delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078447 | ||||||
chr6:32078498
|
A | C | 23 | a0009c0020t0001g0046a0009c0020t0001g0070a0009c0020t0001g0071others(20): Show | 23 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.4375+535T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078498 | ||||||
chr6:32078532
|
G | A | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.4375+501C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078532 | ||||||
chr6:32078565
|
C | A | 14 | a0022c0029t0001g0157a0022c0029t0001g0164a0022c0029t0001g0167others(11): Show | 14 | HG02698.hp1 HG03710.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.4375+468G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078565 | ||||||
chr6:32078805
|
G | A | 1 | a0070c0090t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4375+228C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 11/43 | chr6 | 32078805 | ||||||
chr6:32079396
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4043-31C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079396 | ||||||
chr6:32079491
|
T | C | 11 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(8): Show | 12 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.4043-126A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079491 | ||||||
chr6:32079500
|
G | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.4043-135C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079500 | ||||||
chr6:32079574
|
T | G | 2 | a0008c0045t0001g0336a0008c0045t0001g0337 | 2 | HG01515.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4043-209A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079574 | ||||||
chr6:32079659
|
C | G | 65 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(62): Show | 72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.4043-294G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079659 | ||||||
chr6:32079718
|
C | T | 1 | a0023c0036t0002g0011 | 2 | HG02155.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.4043-353G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079718 | ||||||
chr6:32079960
|
A | C | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4043-595T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32079960 | ||||||
chr6:32080217
|
GT | G | 370 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(367): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.4043-853delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080217 | ||||||
chr6:32080218
|
T | G | 1 | a0007c0005t0002g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4043-853A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080218 | ||||||
chr6:32080367
|
T | C | 1 | a0079c0100t0001g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4042+1001A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080367 | ||||||
chr6:32080456
|
C | G | 1 | a0007c0005t0002g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4042+912G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080456 | ||||||
chr6:32080457
|
G | C | 1 | a0007c0005t0002g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4042+911C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080457 | ||||||
chr6:32080633
|
G | T | 3 | a0009c0020t0001g0070a0009c0020t0001g0071a0009c0020t0001g0072 | 3 | HG00597.hp2 HG02132.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.4042+735C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080633 | ||||||
chr6:32080846
|
T | C | 1 | a0063c0098t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4042+522A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080846 | ||||||
chr6:32080903
|
G | A | 6 | a0026c0033t0002g0152a0026c0033t0002g0153a0026c0033t0002g0154others(3): Show | 6 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.4042+465C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080903 | ||||||
chr6:32080975
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4042+393C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 10/43 | chr6 | 32080975 | ||||||
chr6:32081736
|
C | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3737-63G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081736 | ||||||
chr6:32081960
|
G | C | 1 | a0002c0002t0001g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3736+76C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081960 | ||||||
chr6:32081961
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3736+75G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32081961 | ||||||
chr6:32082029
|
T | A | 1 | a0004c0011t0001g0200 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.3736+7A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 9/43 | chr6 | 32082029 | ||||||
chr6:32082636
|
A | C | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3446-310T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082636 | ||||||
chr6:32082767
|
C | T | 348 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(345): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.3446-441G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082767 | ||||||
chr6:32082844
|
G | A | 2 | a0003c0048t0002g0360a0003c0048t0005g0370 | 2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3446-518C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082844 | ||||||
chr6:32082876
|
C | T | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.3446-550G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082876 | ||||||
chr6:32082981
|
C | T | 18 | a0014c0018t0002g0007a0014c0018t0002g0087a0014c0018t0002g0088others(15): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.3446-655G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32082981 | ||||||
chr6:32083030
|
C | T | 1 | a0054c0122t0004g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3446-704G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083030 | ||||||
chr6:32083123
|
C | T | 1 | a0043c0055t0002g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3446-797G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083123 | ||||||
chr6:32083420
|
A | G | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3445+993T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083420 | ||||||
chr6:32083599
|
C | T | 1 | a0035c0040t0002g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3445+814G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083599 | ||||||
chr6:32083762
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3445+651G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083762 | ||||||
chr6:32083818
|
G | A | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3445+595C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083818 | ||||||
chr6:32083855
|
G | A | 1 | a0011c0009t0002g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3445+558C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32083855 | ||||||
chr6:32084089
|
C | A | 1 | a0065c0093t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3445+324G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32084089 | ||||||
chr6:32084312
|
CTCCAGGA others(5): Show |
C | 26 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(23): Show | 26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.3445+89_3445+100de others(13): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 8/43 | chr6 | 32084312 | ||||||
chr6:32085121
|
C | T | 38 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(35): Show | 44 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.3149-412G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085121 | ||||||
chr6:32085206
|
C | T | 65 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(62): Show | 72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.3149-497G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085206 | ||||||
chr6:32085385
|
A | G | 4 | a0001c0001t0001g0297a0001c0001t0001g0304a0001c0001t0001g0305others(1): Show | 4 | NA18957.hp2 NA18973.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3148+365T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085385 | ||||||
chr6:32085425
|
G | A | 4 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217others(1): Show | 4 | HG02738.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3148+325C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085425 | ||||||
chr6:32085566
|
C | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3148+184G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085566 | ||||||
chr6:32085674
|
C | T | 1 | a0043c0055t0002g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3148+76G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 7/43 | chr6 | 32085674 | ||||||
chr6:32086435
|
C | G | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-317G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086435 | ||||||
chr6:32086569
|
C | A | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-451G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086569 | ||||||
chr6:32086832
|
A | G | 1 | a0012c0015t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2780-714T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086832 | ||||||
chr6:32086882
|
C | T | 3 | a0011c0009t0002g0052a0011c0009t0002g0054a0011c0009t0002g0056 | 3 | HG02080.hp2 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2780-764G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086882 | ||||||
chr6:32086938
|
A | G | 1 | a0099c0060t0001g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2780-820T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086938 | ||||||
chr6:32086965
|
T | G | 1 | a0035c0040t0002g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2780-847A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32086965 | ||||||
chr6:32087089
|
T | C | 1 | a0014c0018t0002g0092 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2780-971A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087089 | ||||||
chr6:32087107
|
G | C | 15 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(12): Show | 17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.2780-989C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087107 | ||||||
chr6:32087157
|
G | A | 33 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(30): Show | 37 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.2780-1039C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087157 | ||||||
chr6:32087210
|
T | C | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2780-1092A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087210 | ||||||
chr6:32087609
|
G | A | 1 | a0023c0053t0002g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2779+1176C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087609 | ||||||
chr6:32087824
|
G | T | 1 | a0069c0083t0002g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2779+961C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087824 | ||||||
chr6:32087922
|
G | T | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2779+863C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32087922 | ||||||
chr6:32088018
|
A | C | 1 | a0002c0002t0001g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2779+767T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088018 | ||||||
chr6:32088165
|
C | G | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2779+620G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088165 | ||||||
chr6:32088573
|
GTAA | G | 348 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(345): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2779+209_2779+211d others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088573 | ||||||
chr6:32088729
|
A | G | 1 | a0003c0003t0002g0353 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2779+56T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 6/43 | chr6 | 32088729 | ||||||
chr6:32089113
|
A | G | 1 | a0010c0084t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2516-65T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089113 | ||||||
chr6:32089130
|
C | G | 5 | a0008c0006t0001g0318a0008c0006t0001g0320a0008c0006t0001g0338others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2516-82G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089130 | ||||||
chr6:32089143
|
TCTGCCCT others(7): Show |
T | 1 | a0095c0064t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2515+66_2515+79del others(14): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 5/43 | chr6 | 32089143 | ||||||
chr6:32089531
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2359-152C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089531 | ||||||
chr6:32089565
|
G | A | 1 | a0013c0014t0001g0293 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2359-186C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089565 | ||||||
chr6:32089848
|
C | T | 7 | a0021c0026t0002g0215a0021c0026t0002g0216a0021c0026t0002g0217others(4): Show | 8 | HG01243.hp1 HG02738.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.2359-469G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089848 | ||||||
chr6:32089850
|
C | T | 58 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(55): Show | 64 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.2359-471G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32089850 | ||||||
chr6:32090113
|
C | T | 1 | a0044c0061t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2359-734G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090113 | ||||||
chr6:32090195
|
T | A | 82 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2359-816A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090195 | ||||||
chr6:32090357
|
G | A | 1 | a0036c0038t0002g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2359-978C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090357 | ||||||
chr6:32090454
|
C | G | 1 | a0008c0045t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2359-1075G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090454 | ||||||
chr6:32090484
|
C | T | 1 | a0043c0055t0002g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2359-1105G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090484 | ||||||
chr6:32090648
|
G | C | 21 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(18): Show | 25 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359-1269C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090648 | ||||||
chr6:32090899
|
C | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0159others(13): Show | 16 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2359-1520G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32090899 | ||||||
chr6:32091171
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2359-1792G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091171 | ||||||
chr6:32091173
|
C | T | 1 | a0057c0071t0002g0203 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2359-1794G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091173 | ||||||
chr6:32091203
|
C | T | 1 | a0001c0109t0001g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2359-1824G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091203 | ||||||
chr6:32091204
|
G | A | 1 | a0011c0009t0002g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2359-1825C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091204 | ||||||
chr6:32091298
|
C | T | 3 | a0022c0029t0001g0167a0022c0059t0001g0165a0099c0060t0001g0163 | 3 | NA18941.hp1 NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2359-1919G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091298 | ||||||
chr6:32091480
|
AT | A | 6 | a0002c0002t0001g0133a0017c0022t0002g0341a0017c0022t0002g0342others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2359-2102delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091480 | ||||||
chr6:32091511
|
CTT | C | 3 | a0020c0025t0001g0005a0020c0025t0001g0174a0048c0066t0002g0175 | 5 | HG02129.hp2 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2359-2134_2359-213 others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091511 | ||||||
chr6:32091623
|
C | T | 17 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(14): Show | 19 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2359-2244G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091623 | ||||||
chr6:32091674
|
A | G | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.2359-2295T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091674 | ||||||
chr6:32091897
|
C | G | 37 | a0003c0003t0001g0350a0003c0003t0002g0048a0003c0003t0002g0244others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2359-2518G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32091897 | ||||||
chr6:32092090
|
A | G | 5 | a0019c0028t0002g0047a0019c0028t0002g0082a0019c0028t0002g0084others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2359-2711T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092090 | ||||||
chr6:32092436
|
G | C | 65 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(62): Show | 72 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2358+2640C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092436 | ||||||
chr6:32092516
|
C | T | 1 | a0009c0027t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2358+2560G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092516 | ||||||
chr6:32092690
|
CA | C | 261 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(258): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.2358+2385delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092690 | ||||||
chr6:32092690
|
CAA | C | 20 | a0001c0001t0001g0273a0012c0015t0001g0335a0014c0018t0002g0007others(17): Show | 21 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.2358+2384_2358+238 others(6): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092690 | ||||||
chr6:32092715
|
A | G | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2358+2361T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092715 | ||||||
chr6:32092719
|
G | C | 14 | a0011c0009t0002g0002a0011c0009t0002g0045a0011c0009t0002g0052others(11): Show | 17 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2358+2357C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092719 | ||||||
chr6:32092780
|
A | G | 12 | a0005c0013t0001g0230a0005c0013t0001g0233a0005c0013t0001g0234others(9): Show | 12 | HG00438.hp1 HG02132.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.2358+2296T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092780 | ||||||
chr6:32092822
|
G | A | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2358+2254C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32092822 | ||||||
chr6:32093038
|
T | C | 6 | a0005c0024t0001g0221a0005c0024t0001g0222a0005c0024t0001g0223others(3): Show | 6 | HG01952.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2358+2038A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093038 | ||||||
chr6:32093365
|
T | A | 1 | a0086c0111t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2358+1711A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093365 | ||||||
chr6:32093448
|
G | A | 4 | a0026c0033t0002g0152a0026c0033t0002g0153a0026c0033t0002g0154others(1): Show | 4 | HG01934.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2358+1628C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093448 | ||||||
chr6:32093562
|
T | G | 20 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0111others(17): Show | 22 | HG04204.hp1 NA18940.hp1 NA18950.hp2 others(19): Show |
intron_variant | MODIFIER | c.2358+1514A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093562 | ||||||
chr6:32093888
|
A | G | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2358+1188T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093888 | ||||||
chr6:32093997
|
G | A | 1 | a0095c0064t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+1079C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32093997 | ||||||
chr6:32094095
|
C | CA | 79 | a0001c0001t0001g0109a0001c0001t0001g0273a0001c0001t0001g0291others(76): Show | 84 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2358+980dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | ||||||
chr6:32094095
|
C | CAA | 35 | a0002c0042t0002g0142a0004c0008t0001g0138a0004c0008t0001g0189others(32): Show | 37 | HG00438.hp1 HG01069.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2358+979_2358+980d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | ||||||
chr6:32094095
|
CA | C | 119 | a0001c0001t0001g0102a0001c0001t0001g0243a0001c0001t0001g0257others(116): Show | 125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.2358+980delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | ||||||
chr6:32094095
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2358+968_2358+980d others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094095 | ||||||
chr6:32094475
|
C | T | 19 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(16): Show | 19 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2358+601G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094475 | ||||||
chr6:32094603
|
T | G | 12 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(9): Show | 14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.2358+473A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094603 | ||||||
chr6:32094691
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2358+385C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094691 | ||||||
chr6:32094910
|
G | A | 82 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2358+166C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094910 | ||||||
chr6:32094981
|
C | G | 1 | a0061c0077t0002g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2358+95G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 4/43 | chr6 | 32094981 | ||||||
chr6:32095325
|
CAG | C | 27 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(24): Show | 27 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2243-136_2243-135d others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/43 | chr6 | 32095325 | ||||||
chr6:32095593
|
G | C | 2 | a0009c0020t0001g0046a0066c0091t0002g0143 | 2 | HG00423.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2242+18C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 3/43 | chr6 | 32095593 | ||||||
chr6:32097483
|
C | G | 1 | a0001c0034t0001g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.404-34G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 2/43 | chr6 | 32097483 | ||||||
chr6:32098345
|
G | A | 2 | a0010c0010t0002g0006a0010c0010t0002g0028 | 3 | HG01099.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-139C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098345 | ||||||
chr6:32098366
|
T | C | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-160A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098366 | ||||||
chr6:32098400
|
T | C | 81 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8-194A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098400 | ||||||
chr6:32098443
|
C | T | 4 | a0010c0010t0002g0006a0010c0010t0002g0024a0010c0010t0002g0027others(1): Show | 5 | HG01074.hp1 HG01099.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-237G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098443 | ||||||
chr6:32098456
|
T | TTTTTG | 25 | a0002c0002t0001g0008a0005c0013t0001g0040a0005c0013t0001g0230others(22): Show | 26 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-255_-8-251dupCA others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | ||||||
chr6:32098456
|
TTTTTG | T | 8 | a0004c0011t0001g0178a0004c0011t0001g0179a0004c0011t0001g0192others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-255_-8-251delCA others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | ||||||
chr6:32098456
|
TTTTTGTT others(3): Show |
T | 26 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(23): Show | 26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-260_-8-251delCA others(8): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098456 | ||||||
chr6:32098543
|
C | T | 15 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(12): Show | 17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-337G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098543 | ||||||
chr6:32098670
|
G | A | 37 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-464C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098670 | ||||||
chr6:32098858
|
T | A | 1 | a0094c0124t0002g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-652A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098858 | ||||||
chr6:32098936
|
A | G | 1 | a0010c0010t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-730T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098936 | ||||||
chr6:32098969
|
T | C | 2 | a0033c0043t0002g0032a0033c0043t0002g0137 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-763A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098969 | ||||||
chr6:32098988
|
C | T | 26 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(23): Show | 26 | HG00140.hp1 HG01515.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-782G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32098988 | ||||||
chr6:32099038
|
C | T | 15 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(12): Show | 17 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-832G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099038 | ||||||
chr6:32099042
|
T | A | 348 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(345): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-8-836A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099042 | ||||||
chr6:32099226
|
T | C | 16 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(13): Show | 18 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1020A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099226 | ||||||
chr6:32099235
|
CT | C | 131 | a0001c0001t0001g0031a0001c0001t0001g0291a0002c0002t0001g0111others(128): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-8-1030delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | ||||||
chr6:32099235
|
CTT | C | 181 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(178): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-8-1031_-8-1030del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | ||||||
chr6:32099235
|
CTTT | C | 20 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(17): Show | 20 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1032_-8-1030del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099235 | ||||||
chr6:32099658
|
T | G | 17 | a0001c0001t0001g0159a0001c0001t0001g0160a0011c0009t0002g0002others(14): Show | 20 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-1452A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099658 | ||||||
chr6:32099659
|
TG | T | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1454delC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099659 | ||||||
chr6:32099661
|
G | C | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1455C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099661 | ||||||
chr6:32099726
|
GA | G | 55 | a0001c0001t0001g0298a0003c0003t0001g0350a0003c0003t0002g0251others(52): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-8-1521delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099726 | ||||||
chr6:32099946
|
T | TA | 87 | a0001c0001t0001g0031a0001c0001t0001g0243a0001c0001t0001g0268others(84): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-1741dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | ||||||
chr6:32099946
|
T | TAA | 11 | a0012c0015t0001g0332a0012c0015t0001g0335a0012c0099t0001g0333others(8): Show | 11 | HG01891.hp1 HG01975.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-1742_-8-1741dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | ||||||
chr6:32099946
|
TA | T | 23 | a0004c0008t0001g0177a0006c0004t0001g0199a0007c0005t0002g0004others(20): Show | 27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-1741delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099946 | ||||||
chr6:32099966
|
AAAAAC | A | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1765_-8-1761del others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32099966 | ||||||
chr6:32100065
|
A | G | 1 | a0002c0002t0001g0008 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-8-1859T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100065 | ||||||
chr6:32100107
|
CT | C | 41 | a0001c0001t0001g0305a0001c0007t0001g0280a0001c0007t0001g0288others(38): Show | 41 | HG00140.hp1 HG01071.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-8-1902delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100107 | ||||||
chr6:32100173
|
C | T | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1967G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100173 | ||||||
chr6:32100190
|
C | T | 24 | a0001c0001t0001g0031a0009c0020t0001g0046a0009c0020t0001g0070others(21): Show | 24 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-1984G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100190 | ||||||
chr6:32100328
|
C | T | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2122G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100328 | ||||||
chr6:32100405
|
G | C | 1 | a0033c0043t0002g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-2199C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100405 | ||||||
chr6:32100653
|
G | A | 1 | a0052c0121t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-2447C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100653 | ||||||
chr6:32100714
|
G | A | 1 | a0054c0122t0004g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-8-2508C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100714 | ||||||
chr6:32100718
|
C | T | 2 | a0014c0018t0002g0007a0014c0081t0002g0079 | 3 | HG00323.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-8-2512G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100718 | ||||||
chr6:32100845
|
G | T | 1 | a0004c0062t0001g0176 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-2639C>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32100845 | ||||||
chr6:32101029
|
G | C | 1 | a0043c0055t0002g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8-2823C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101029 | ||||||
chr6:32101077
|
C | CA | 52 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160others(49): Show | 55 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-2872dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
C | CAA | 55 | a0001c0001t0001g0102a0001c0001t0001g0145a0001c0001t0001g0226others(52): Show | 55 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-2873_-8-2872dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
C | CAAA | 29 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(26): Show | 31 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-2874_-8-2872dup others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
C | CAAAA | 8 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0001g0276others(5): Show | 8 | HG01358.hp2 HG02055.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-2875_-8-2872dup others(4): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
CA | C | 53 | a0002c0002t0001g0115a0002c0012t0002g0038a0003c0003t0002g0244others(50): Show | 55 | HG00140.hp1 HG00408.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-2872delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
CAA | C | 25 | a0003c0003t0002g0251a0003c0003t0002g0313a0003c0003t0002g0353others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-2873_-8-2872del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101077
|
CAAA | C | 11 | a0003c0003t0001g0350a0003c0003t0002g0351a0003c0003t0002g0352others(8): Show | 11 | HG00408.hp2 HG00609.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-2874_-8-2872del others(3): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101077 | ||||||
chr6:32101108
|
G | A | 10 | a0004c0008t0001g0315a0006c0004t0001g0001a0006c0004t0001g0195others(7): Show | 14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-2902C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101108 | ||||||
chr6:32101179
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18979.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-8-2973T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101179 | ||||||
chr6:32101455
|
A | T | 1 | a0012c0015t0001g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8-3249T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101455 | ||||||
chr6:32101491
|
G | A | 1 | a0012c0015t0001g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8-3285C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101491 | ||||||
chr6:32101512
|
A | T | 2 | a0054c0122t0004g0228a0055c0123t0004g0227 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-8-3306T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101512 | ||||||
chr6:32101588
|
C | CT | 66 | a0001c0001t0001g0100a0001c0001t0001g0145a0001c0001t0001g0151others(63): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-8-3383dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101588 | ||||||
chr6:32101588
|
C | CTT | 63 | a0002c0002t0001g0114a0002c0002t0001g0204a0002c0012t0002g0037others(60): Show | 70 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.-8-3384_-8-3383dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101588 | ||||||
chr6:32101608
|
T | C | 1 | a0001c0109t0001g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-3402A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101608 | ||||||
chr6:32101855
|
C | G | 1 | a0002c0042t0002g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8-3649G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32101855 | ||||||
chr6:32102029
|
G | C | 378 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(375): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.-8-3823C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102029 | ||||||
chr6:32102064
|
C | T | 1 | a0093c0116t0001g0378 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-3858G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102064 | ||||||
chr6:32102236
|
G | C | 1 | a0096c0057t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8-4030C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102236 | ||||||
chr6:32102292
|
G | A | 79 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-8-4086C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102292 | ||||||
chr6:32102297
|
G | A | 14 | a0001c0007t0001g0279a0001c0007t0001g0280a0001c0007t0001g0281others(11): Show | 14 | HG00733.hp1 HG01346.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-4091C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102297 | ||||||
chr6:32102462
|
A | G | 11 | a0007c0005t0002g0004a0007c0005t0002g0042a0007c0005t0002g0058others(8): Show | 13 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-4256T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102462 | ||||||
chr6:32102498
|
A | G | 1 | a0063c0098t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-4292T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102498 | ||||||
chr6:32102570
|
AAAAAAAG | A | 149 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(146): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-8-4371_-8-4365del others(7): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102570 | ||||||
chr6:32102585
|
A | T | 1 | a0026c0033t0002g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-8-4379T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102585 | ||||||
chr6:32102746
|
CCT | C | 35 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(32): Show | 39 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-8-4542_-8-4541del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102746 | ||||||
chr6:32102825
|
CA | C | 5 | a0016c0017t0003g0207a0016c0017t0003g0208a0016c0017t0003g0209others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4620delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102825 | ||||||
chr6:32102913
|
T | A | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4707A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102913 | ||||||
chr6:32102938
|
A | C | 3 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038 | 3 | HG00408.hp1 HG00597.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-8-4732T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32102938 | ||||||
chr6:32103061
|
T | C | 15 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(12): Show | 16 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-4855A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103061 | ||||||
chr6:32103108
|
T | C | 1 | a0086c0111t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8-4902A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103108 | ||||||
chr6:32103114
|
T | G | 1 | a0087c0105t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-8-4908A>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103114 | ||||||
chr6:32103187
|
A | T | 1 | a0010c0010t0002g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-4981T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103187 | ||||||
chr6:32103231
|
G | A | 15 | a0001c0007t0001g0278a0001c0007t0001g0279a0001c0007t0001g0280others(12): Show | 15 | HG00639.hp1 HG00733.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-5025C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103231 | ||||||
chr6:32103233
|
G | A | 27 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(24): Show | 27 | HG00140.hp1 HG01109.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-5027C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103233 | ||||||
chr6:32103240
|
C | G | 348 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(345): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-8-5034G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103240 | ||||||
chr6:32103250
|
G | A | 1 | a0002c0096t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-5044C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103250 | ||||||
chr6:32103271
|
T | TA | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-5066dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103271 | ||||||
chr6:32103335
|
C | T | 3 | a0001c0001t0001g0249a0041c0049t0002g0247a0041c0049t0002g0248 | 3 | HG00639.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-8-5129G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103335 | ||||||
chr6:32103422
|
TC | T | 17 | a0001c0001t0001g0159a0001c0001t0001g0160a0011c0009t0002g0002others(14): Show | 20 | HG00642.hp2 HG00733.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-5217delG | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103422 | ||||||
chr6:32103429
|
C | CA | 213 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(210): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-8-5224dupT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103429 | ||||||
chr6:32103429
|
CA | C | 8 | a0002c0002t0001g0111a0003c0003t0002g0048a0009c0027t0001g0050others(5): Show | 8 | HG02486.hp1 HG02965.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-5224delT | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103429 | ||||||
chr6:32103478
|
C | A | 1 | a0002c0097t0002g0039 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-8-5272G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103478 | ||||||
chr6:32103481
|
C | G | 11 | a0012c0015t0001g0326a0012c0015t0001g0327a0012c0015t0001g0330others(8): Show | 11 | HG02622.hp1 HG02735.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-5275G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103481 | ||||||
chr6:32103491
|
CCA | C | 13 | a0008c0006t0001g0220a0008c0006t0001g0317a0008c0006t0001g0318others(10): Show | 13 | HG00140.hp1 HG01884.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-5287_-8-5286del others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103491 | ||||||
chr6:32103607
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-5401G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103607 | ||||||
chr6:32103662
|
A | T | 1 | a0001c0109t0001g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-5456T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103662 | ||||||
chr6:32103727
|
C | CT | 44 | a0001c0001t0001g0245a0002c0012t0002g0036a0003c0003t0002g0244others(41): Show | 44 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-9+5453dupA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | ||||||
chr6:32103727
|
C | CTT | 6 | a0008c0006t0001g0317a0017c0022t0002g0341a0017c0022t0002g0342others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+5452_-9+5453dup others(2): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | ||||||
chr6:32103727
|
CT | C | 15 | a0001c0001t0001g0305a0002c0002t0001g0135a0004c0011t0001g0200others(12): Show | 17 | HG01074.hp2 HG01934.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+5453delA | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103727 | ||||||
chr6:32103806
|
A | C | 1 | a0009c0092t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9+5375T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103806 | ||||||
chr6:32103812
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-9+5369G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103812 | ||||||
chr6:32103860
|
T | C | 150 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(147): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9+5321A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103860 | ||||||
chr6:32103889
|
A | G | 21 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(18): Show | 21 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9+5292T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32103889 | ||||||
chr6:32104116
|
C | T | 348 | a0001c0001t0001g0031a0001c0001t0001g0100a0001c0001t0001g0102others(345): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-9+5065G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104116 | ||||||
chr6:32104208
|
C | T | 1 | a0007c0005t0002g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-9+4973G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104208 | ||||||
chr6:32104434
|
A | C | 15 | a0022c0029t0001g0164a0022c0029t0001g0167a0022c0059t0001g0165others(12): Show | 15 | HG02129.hp1 HG02698.hp1 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+4747T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104434 | ||||||
chr6:32104596
|
C | T | 1 | a0010c0084t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9+4585G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104596 | ||||||
chr6:32104618
|
A | G | 18 | a0005c0013t0001g0040a0005c0013t0001g0230a0005c0013t0001g0233others(15): Show | 18 | HG00438.hp1 HG01952.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9+4563T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104618 | ||||||
chr6:32104643
|
C | T | 1 | a0005c0013t0001g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9+4538G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32104643 | ||||||
chr6:32105152
|
T | A | 1 | a0070c0090t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-9+4029A>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105152 | ||||||
chr6:32105163
|
C | T | 64 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(61): Show | 71 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.-9+4018G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105163 | ||||||
chr6:32105463
|
GAGGGC | G | 4 | a0002c0012t0002g0036a0002c0012t0002g0037a0002c0012t0002g0038others(1): Show | 4 | HG00408.hp1 HG00597.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+3713_-9+3717del others(5): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105463 | ||||||
chr6:32105581
|
C | T | 1 | a0088c0104t0001g0306 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-9+3600G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105581 | ||||||
chr6:32105639
|
C | T | 1 | a0037c0041t0001g0035 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9+3542G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105639 | ||||||
chr6:32105762
|
A | T | 1 | a0010c0010t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+3419T>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105762 | ||||||
chr6:32105800
|
A | C | 1 | a0005c0013t0001g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9+3381T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105800 | ||||||
chr6:32105923
|
C | T | 57 | a0004c0008t0001g0033a0004c0008t0001g0138a0004c0008t0001g0177others(54): Show | 58 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+3258G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105923 | ||||||
chr6:32105929
|
A | G | 2 | a0033c0043t0002g0032a0033c0043t0002g0137 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+3252T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32105929 | ||||||
chr6:32106122
|
G | C | 1 | a0060c0117t0002g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9+3059C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106122 | ||||||
chr6:32106131
|
T | TG | 47 | a0001c0001t0001g0031a0001c0001t0001g0145a0001c0001t0001g0159others(44): Show | 48 | HG00408.hp2 HG00609.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9+3049dupC | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106131 | ||||||
chr6:32106134
|
G | C | 7 | a0007c0005t0002g0147a0021c0026t0002g0215a0021c0026t0002g0216others(4): Show | 8 | HG01884.hp1 HG02738.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3047C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106134 | ||||||
chr6:32106136
|
G | C | 10 | a0010c0010t0002g0006a0010c0010t0002g0024a0010c0010t0002g0027others(7): Show | 11 | HG00642.hp1 HG01074.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+3045C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106136 | ||||||
chr6:32106140
|
G | C | 1 | a0002c0002t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-9+3041C>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106140 | ||||||
chr6:32106196
|
T | C | 15 | a0001c0001t0001g0151a0003c0003t0002g0313a0015c0016t0002g0355others(12): Show | 15 | HG00408.hp2 HG00609.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+2985A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106196 | ||||||
chr6:32106247
|
A | G | 14 | a0001c0001t0001g0242a0001c0001t0001g0243a0003c0003t0001g0350others(11): Show | 14 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+2934T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106247 | ||||||
chr6:32106256
|
G | A | 3 | a0008c0006t0001g0338a0008c0006t0001g0339a0008c0006t0001g0340 | 3 | HG01884.hp2 HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-9+2925C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106256 | ||||||
chr6:32106301
|
G | A | 1 | a0022c0029t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+2880C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106301 | ||||||
chr6:32106514
|
C | T | 1 | a0004c0011t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+2667G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106514 | ||||||
chr6:32106657
|
C | T | 1 | a0022c0029t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+2524G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106657 | ||||||
chr6:32106672
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9+2509G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106672 | ||||||
chr6:32106734
|
C | T | 1 | a0073c0087t0002g0030 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-9+2447G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106734 | ||||||
chr6:32106741
|
C | G | 13 | a0010c0010t0001g0017a0010c0010t0002g0006a0010c0010t0002g0019others(10): Show | 14 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+2440G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106741 | ||||||
chr6:32106772
|
T | C | 1 | a0015c0016t0006g0376 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-9+2409A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32106772 | ||||||
chr6:32107027
|
T | C | 31 | a0004c0008t0001g0315a0006c0004t0001g0001a0006c0004t0001g0316others(28): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9+2154A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107027 | ||||||
chr6:32107078
|
C | T | 1 | a0071c0089t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-9+2103G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107078 | ||||||
chr6:32107114
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9+2067A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107114 | ||||||
chr6:32107137
|
C | T | 1 | a0010c0010t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+2044G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107137 | ||||||
chr6:32107157
|
C | T | 1 | a0028c0035t0001g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+2024G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107157 | ||||||
chr6:32107220
|
C | A | 6 | a0001c0001t0001g0159a0001c0001t0001g0160a0022c0029t0001g0157others(3): Show | 7 | HG02083.hp2 HG02155.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+1961G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107220 | ||||||
chr6:32107526
|
T | C | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+1655A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107526 | ||||||
chr6:32107582
|
T | C | 5 | a0017c0022t0002g0341a0017c0022t0002g0342a0017c0022t0002g0343others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+1599A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107582 | ||||||
chr6:32107766
|
A | C | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1415T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107766 | ||||||
chr6:32107767
|
C | A | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1414G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107767 | ||||||
chr6:32107768
|
A | C | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1413T>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107768 | ||||||
chr6:32107770
|
ATGGGGGT others(8): Show |
A | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1396_-9+1410del others(15): Show |
TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107770 | ||||||
chr6:32107786
|
T | C | 204 | a0001c0001t0001g0226a0001c0001t0001g0242a0001c0001t0001g0243others(201): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-9+1395A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107786 | ||||||
chr6:32107787
|
G | A | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1394C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107787 | ||||||
chr6:32107789
|
C | G | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1392G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107789 | ||||||
chr6:32107790
|
C | A | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1391G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107790 | ||||||
chr6:32107792
|
C | G | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1389G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107792 | ||||||
chr6:32107799
|
C | T | 1 | a0056c0118t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+1382G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107799 | ||||||
chr6:32107963
|
A | G | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+1218T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107963 | ||||||
chr6:32107988
|
G | A | 2 | a0027c0052t0002g0013a0027c0125t0002g0377 | 3 | HG01884.hp1 HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+1193C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32107988 | ||||||
chr6:32108023
|
A | G | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+1158T>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108023 | ||||||
chr6:32108059
|
G | A | 6 | a0001c0001t0001g0226a0005c0024t0001g0221a0005c0024t0001g0222others(3): Show | 6 | HG01952.hp1 HG02165.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1122C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108059 | ||||||
chr6:32108335
|
G | A | 1 | a0047c0065t0001g0346 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+846C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108335 | ||||||
chr6:32108361
|
C | G | 2 | a0007c0005t0002g0348a0056c0118t0002g0015 | 2 | HG01934.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-9+820G>C | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108361 | ||||||
chr6:32108561
|
G | A | 1 | a0006c0004t0001g0347 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9+620C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108561 | ||||||
chr6:32108578
|
T | C | 3 | a0053c0119t0004g0229a0054c0122t0004g0228a0055c0123t0004g0227 | 3 | HG02109.hp2 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+603A>G | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108578 | ||||||
chr6:32108640
|
C | T | 1 | a0067c0082t0002g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+541G>A | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108640 | ||||||
chr6:32108722
|
G | A | 119 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(116): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-9+459C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32108722 | ||||||
chr6:32109065
|
C | A | 31 | a0003c0003t0001g0350a0003c0003t0002g0351a0003c0003t0002g0352others(28): Show | 32 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-9+116G>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32109065 | ||||||
chr6:32109130
|
G | A | 3 | a0064c0079t0001g0379a0076c0080t0001g0380a0093c0116t0001g0378 | 3 | HG01891.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+51C>T | TNXB | ENSG00000168477.21 | transcript | ENST00000644971.2 | protein_coding | 1/43 | chr6 | 32109130 |